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Hidradenitis suppurativa

Abstract

Hidradenitis suppurativa (HS; also designated as acne inversa) is a chronic inflammatory disorder, which affects the intertriginous skin and is associated with numerous systemic comorbidities. The estimated prevalence of HS is ~1% in most studied countries. Typically starting in early adulthood, cutaneous inflamed nodules, abscesses and pus-discharging tunnels develop in axillary, inguinal, gluteal and perianal body sites. The comorbidities of HS include metabolic and cardiovascular disorders, which contribute to reduced life expectancy. A genetic predisposition, smoking, obesity and hormonal factors are established aetiological factors for HS. Cutaneous changes seem to start around hair follicles and involve activation of cells of the innate and adaptive immune systems, with pivotal roles for pro-inflammatory cytokines such as tumour necrosis factor, IL-1β and IL-17. The unrestricted and chronic immune response eventually leads to severe pain, pus discharge, irreversible tissue destruction and scar development. HS has profound negative effects on patients’ quality of life, which often culminate in social withdrawal, unemployment, depression and suicidal thoughts. The therapeutic options for HS comprise antibiotic treatment, neutralization of tumour necrosis factor and surgical intervention together with lifestyle modification. Nevertheless, there is an enormous need for awareness of HS, understanding of its pathogenesis and novel treatments.

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Fig. 1: Histology of hidradenitis suppurativa lesions.
Fig. 2: Pathogenesis of HS — initial pathogenetic events.
Fig. 3: Pathogenesis of HS — progression to advanced disease.
Fig. 4: Typical skin lesions of hidradenitis suppurativa.
Fig. 5: Hidradenitis suppurativa management.

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References

  1. Saunte, D. M. L. & Jemec, G. B. E. Hidradenitis suppurativa: advances in diagnosis and treatment. JAMA 318, 2019–2032 (2017).

    Article  PubMed  Google Scholar 

  2. Ingram, J. R. et al. Population-based clinical practice research datalink study using algorithm modelling to identify the true burden of hidradenitis suppurativa. Br. J. Dermatol. 178, 917–924 (2018). This paper is a well-conducted registry study providing a realistic estimate of HS prevalence.

    Article  CAS  PubMed  Google Scholar 

  3. Theut Riis, P., Thorlacius, L., Knudsen List, E. & Jemec, G. B. E. A pilot study of unemployment in patients with hidradenitis suppurativa in Denmark. Br. J. Dermatol. 176, 1083–1085 (2017).

    Article  CAS  PubMed  Google Scholar 

  4. Matusiak, L., Bieniek, A. & Szepietowski, J. C. Hidradenitis suppurativa markedly decreases quality of life and professional activity. J. Am. Acad. Dermatol. 62, 706–708 (2010).

    Article  PubMed  Google Scholar 

  5. Wolk, K. et al. Deficiency of IL-22 contributes to a chronic inflammatory disease: pathogenetic mechanisms in acne inversa. J. Immunol. 186, 1228–1239 (2011). This paper is the first investigation of the role of cytokines related to activated lymphocytes (for example, IL-17, IL-22, IL-26 and IFNγ) and myeloid cells (for example, IL-1β and IL-10), the elements of their pathways and their consequences in the skin of patients with HS.

    Article  CAS  PubMed  Google Scholar 

  6. Sabat, R. et al. Increased prevalence of metabolic syndrome in patients with acne inversa. PLoS One 7, e31810 (2012). This paper is a comprehensive prospective case–control study that first reported the high prevalence of the metabolic syndrome in patients with HS, an observation most striking among young patients.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Shlyankevich, J., Chen, A. J., Kim, G. E. & Kimball, A. B. Hidradenitis suppurativa is a systemic disease with substantial comorbidity burden: a chart-verified case-control analysis. J. Am. Acad. Dermatol. 71, 1144–1150 (2014).

    Article  PubMed  Google Scholar 

  8. Schneider-Burrus, S. et al. High prevalence of back pain and axial spondyloarthropathy in patients with hidradenitis suppurativa. Dermatology 232, 606–612 (2016).

    Article  PubMed  Google Scholar 

  9. Richette, P. et al. Hidradenitis suppurativa associated with spondyloarthritis — results from a multicenter national prospective study. J. Rheumatol. 41, 490–494 (2014).

    Article  PubMed  Google Scholar 

  10. Deckers, I. E. et al. Inflammatory bowel disease is associated with hidradenitis suppurativa: results from a multicenter cross-sectional study. J. Am. Acad. Dermatol. 76, 49–53 (2017).

    Article  PubMed  Google Scholar 

  11. Egeberg, A. et al. Prevalence and risk of inflammatory bowel disease in patients with hidradenitis suppurativa. J. Invest. Dermatol. 137, 1060–1064 (2017).

    Article  CAS  PubMed  Google Scholar 

  12. Gonzalez-Lopez, M. A. et al. Increased prevalence of subclinical atherosclerosis in patients with hidradenitis suppurativa (HS). J. Am. Acad. Dermatol. 75, 329–335 (2016).

    Article  PubMed  Google Scholar 

  13. Vazquez, B. G., Alikhan, A., Weaver, A. L., Wetter, D. A. & Davis, M. D. Incidence of hidradenitis suppurativa and associated factors: a population-based study of Olmsted County, Minnesota. J. Invest. Dermatol. 133, 97–103 (2013).

    Article  CAS  PubMed  Google Scholar 

  14. Kurek, A., Johanne Peters, E. M., Sabat, R., Sterry, W. & Schneider-Burrus, S. Depression is a frequent co-morbidity in patients with acne inversa. J. Dtsch. Dermatol. Ges. 11, 743–750 (2013).

    PubMed  Google Scholar 

  15. Jemec, G. B. & Kimball, A. B. Hidradenitis suppurativa: epidemiology and scope of the problem. J. Am. Acad. Dermatol. 73, S4–S7 (2015).

    Article  PubMed  Google Scholar 

  16. Ingvarsson, G. Regional variation of hidradenitis suppurativa in the Norwegian patient registry during a 5-year period may describe professional awareness of the disease, not changes in prevalence. Br. J. Dermatol. 176, 274–275 (2017).

    Article  CAS  PubMed  Google Scholar 

  17. Sung, S. & Kimball, A. B. Counterpoint: analysis of patient claims data to determine the prevalence of hidradenitis suppurativa in the United States. J. Am. Acad. Dermatol. 69, 818–819 (2013).

    Article  PubMed  Google Scholar 

  18. Kurokawa, I., Hayashi, N. & Japan Acne Research, S. Questionnaire surveillance of hidradenitis suppurativa in Japan. J. Dermatol. 42, 747–749 (2015).

    Article  PubMed  Google Scholar 

  19. Lee, J. H., Kwon, H. S., Jung, H. M., Kim, G. M. & Bae, J. M. Prevalence and comorbidities associated with hidradenitis suppurativa in Korea: a nationwide population-based study. J. Eur. Acad. Dermatol. Venereol. 32, 1784–1790 (2018).

    Article  CAS  PubMed  Google Scholar 

  20. Garg, A., Kirby, J. S., Lavian, J., Lin, G. & Strunk, A. Sex- and age-adjusted population analysis of prevalence estimates for hidradenitis suppurativa in the United States. JAMA Dermatol. 153, 760–764 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  21. Jemec, G. B., Heidenheim, M. & Nielsen, N. H. The prevalence of hidradenitis suppurativa and its potential precursor lesions. J. Am. Acad. Dermatol. 35, 191–194 (1996).

    Article  CAS  PubMed  Google Scholar 

  22. Calao, M. et al. Hidradenitis suppurativa (HS) prevalence, demographics and management pathways in Australia: a population-based cross-sectional study. PLoS One 13, e0200683 (2018). This paper is a comprehensive study describing the prevalence of HS in the general population.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Zouboulis, C. C. et al. Development and validation of the international hidradenitis suppurativa severity score system (IHS4), a novel dynamic scoring system to assess HS severity. Br. J. Dermatol. 177, 1401–1409 (2017). This paper describes the development of the IHS4, which has the potential to become the gold standard for the classification of patients with HS.

    Article  CAS  PubMed  Google Scholar 

  24. Deckers, I. E., van der Zee, H. H., Boer, J. & Prens, E. P. Correlation of early-onset hidradenitis suppurativa with stronger genetic susceptibility and more widespread involvement. J. Am. Acad. Dermatol. 72, 485–488 (2015).

    Article  PubMed  Google Scholar 

  25. Yang, J. H. et al. Demographic and clinical features of hidradenitis suppurativa in Korea. J. Dermatol. 45, 1389–1395 (2018).

    Article  PubMed  Google Scholar 

  26. Kromann, C. B. et al. Risk factors, clinical course and long-term prognosis in hidradenitis suppurativa: a cross-sectional study. Br. J. Dermatol. 171, 819–824 (2014).

    Article  CAS  PubMed  Google Scholar 

  27. Egeberg, A., Gislason, G. H. & Hansen, P. R. Risk of major adverse cardiovascular events and all-cause mortality in patients with hidradenitis suppurativa. JAMA Dermatol. 152, 429–434 (2016).

    Article  PubMed  Google Scholar 

  28. Ingram, J. R. The genetics of hidradenitis suppurativa. Dermatol. Clin. 34, 23–28 (2016).

    Article  CAS  PubMed  Google Scholar 

  29. von der Werth, J. M. & Williams, H. C. The natural history of hidradenitis suppurativa. J. Eur. Acad. Dermatol. Venereol. 14, 389–392 (2000).

    Article  PubMed  Google Scholar 

  30. Wang, B. et al. Gamma-secretase gene mutations in familial acne inversa. Science 330, 1065 (2010). This paper is the first study to demonstrate loss of function mutations in genes encoding γ-secretase, cumulatively found among members of Chinese families with severe HS.

    Article  CAS  PubMed  Google Scholar 

  31. Haapasalo, A. & Kovacs, D. M. The many substrates of presenilin/gamma-secretase. J. Alzheimers Dis. 25, 3–28 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Frew, J. W., Vekic, D. A., Woods, J. & Cains, G. D. A systematic review and critical evaluation of reported pathogenic sequence variants in hidradenitis suppurativa. Br. J. Dermatol. 177, 987–998 (2017).

    Article  CAS  PubMed  Google Scholar 

  33. Pan, Y. et al. γ-Secretase functions through Notch signaling to maintain skin appendages but is not required for their patterning or initial morphogenesis. Dev. Cell 7, 731–743 (2004).

    Article  CAS  PubMed  Google Scholar 

  34. O’Sullivan Coyne, G., Woodring, T. S., Lee, C. R., Chen, A. P. & Kong, H. H. Hidradenitis suppurativa-like lesions associated with pharmacologic inhibition of gamma-secretase. J. Invest. Dermatol. 138, 979–981 (2018).

    Article  PubMed  CAS  Google Scholar 

  35. Aubin-Houzelstein, G. Notch signaling and the developing hair follicle. Adv. Exp. Med. Biol. 727, 142–160 (2012).

    Article  CAS  PubMed  Google Scholar 

  36. Asano, N., Watanabe, T., Kitani, A., Fuss, I. J. & Strober, W. Notch1 signaling and regulatory T cell function. J. Immunol. 180, 2796–2804 (2008).

    Article  CAS  PubMed  Google Scholar 

  37. Ali, N. et al. Regulatory T cells in skin facilitate epithelial stem cell differentiation. Cell 169, 1119–1129 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Lowell, S., Jones, P., Le Roux, I., Dunne, J. & Watt, F. M. Stimulation of human epidermal differentiation by delta-notch signalling at the boundaries of stem-cell clusters. Curr. Biol. 10, 491–500 (2000).

    Article  CAS  PubMed  Google Scholar 

  39. Alam, M. S. et al. Notch signaling drives IL-22 secretion in CD4+ T cells by stimulating the aryl hydrocarbon receptor. Proc. Natl Acad. Sci. USA 107, 5943–5948 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  40. Pang, B. et al. Elevated Notch1 enhances interleukin-22 production by CD4+ T cells via aryl hydrocarbon receptor in patients with lung adenocarcinoma. Biosci. Rep. 38, BSR20181922 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  41. Wolk, K. et al. IL-22 increases the innate immunity of tissues. Immunity 21, 241–254 (2004).

    Article  CAS  PubMed  Google Scholar 

  42. Pink, A. E. et al. Mutations in the gamma-secretase genes NCSTN, PSENEN, and PSEN1 underlie rare forms of hidradenitis suppurativa (acne inversa). J. Invest. Dermatol. 132, 2459–2461 (2012).

    Article  CAS  PubMed  Google Scholar 

  43. Liu, M. et al. Genetic analysis of NCSTN for potential association with hidradenitis suppurativa in familial and nonfamilial patients. Br. J. Dermatol. 175, 414–416 (2016).

    Article  CAS  PubMed  Google Scholar 

  44. Ingram, J. R., Wood, M., John, B., Butler, R. & Anstey, A. V. Absence of pathogenic gamma-secretase mutations in a South Wales cohort of familial and sporadic hidradenitis suppurativa (acne inversa). Br. J. Dermatol. 168, 874–876 (2013).

    Article  CAS  PubMed  Google Scholar 

  45. Giatrakos, S. et al. Haplotypes of IL-12Rbeta1 impact on the clinical phenotype of hidradenitis suppurativa. Cytokine 62, 297–301 (2013).

    Article  CAS  PubMed  Google Scholar 

  46. Vural, S. et al. Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case-control study. Br. J. Dermatol. 180, 1459–1467 (2019).

    Article  CAS  PubMed  Google Scholar 

  47. Revuz, J. E. et al. Prevalence and factors associated with hidradenitis suppurativa: results from two case-control studies. J. Am. Acad. Dermatol. 59, 596–601 (2008).

    Article  PubMed  Google Scholar 

  48. Konig, A., Lehmann, C., Rompel, R. & Happle, R. Cigarette smoking as a triggering factor of hidradenitis suppurativa. Dermatology 198, 261–264 (1999).

    Article  CAS  PubMed  Google Scholar 

  49. Hana, A. et al. Functional significance of non-neuronal acetylcholine in skin epithelia. Life Sci. 80, 2214–2220 (2007).

    Article  CAS  PubMed  Google Scholar 

  50. Radek, K. A. et al. Neuroendocrine nicotinic receptor activation increases susceptibility to bacterial infections by suppressing antimicrobial peptide production. Cell Host Microbe 7, 277–289 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Wu, Y. et al. Nicotine enhances Staphylococcus epidermidis biofilm formation by altering the bacterial autolysis, extracellular DNA releasing, and polysaccharide intercellular adhesin production. Front. Microbiol. 9, 2575 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  52. Wittebole, X. et al. Nicotine exposure alters in vivo human responses to endotoxin. Clin. Exp. Immunol. 147, 28–34 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  53. Boer, J. Should hidradenitis suppurativa be included in dermatoses showing Koebnerization? Is it friction or fiction? Dermatology 233, 47–52 (2017).

    Article  PubMed  Google Scholar 

  54. Alikhan, A., Lynch, P. J. & Eisen, D. B. Hidradenitis suppurativa: a comprehensive review. J. Am. Acad. Dermatol. 60, 539–561; quiz 562–563 (2009).

    Article  PubMed  Google Scholar 

  55. Riis, P. T., Ring, H. C., Themstrup, L. & Jemec, G. B. The role of androgens and estrogens in hidradenitis suppurativa — a systematic review. Acta Dermatovenerol. Croat. 24, 239–249 (2016).

    PubMed  Google Scholar 

  56. Karagiannidis, I., Nikolakis, G., Sabat, R. & Zouboulis, C. C. Hidradenitis suppurativa/acne inversa: an endocrine skin disorder? Rev. Endocr. Metab. Disord. 17, 335–341 (2016).

    Article  CAS  PubMed  Google Scholar 

  57. Gauntner, T. D. Hormonal, stem cell and Notch signalling as possible mechanisms of disease in hidradenitis suppurativa: a systems-level transcriptomic analysis. Br. J. Dermatol. 180, 203–204 (2019).

    Article  PubMed  Google Scholar 

  58. Jenei, A. et al. Apocrine gland-rich skin has a non-inflammatory IL-17-related immune milieu, that turns to inflammatory IL-17-mediated disease in hidradenitis suppurativa. J. Invest. Dermatol. 139, 964–968 (2019).

    Article  CAS  PubMed  Google Scholar 

  59. Kamp, S. et al. Hidradenitis suppurativa: a disease of the absent sebaceous gland? Sebaceous gland number and volume are significantly reduced in uninvolved hair follicles from patients with hidradenitis suppurativa. Br. J. Dermatol. 164, 1017–1022 (2011).

    Article  CAS  PubMed  Google Scholar 

  60. Naik, H. B. et al. Are bacteria infectious pathogens in hidradenitis suppurativa? Debate at the symposium for hidradenitis suppurativa advances meeting, November 2017. J. Invest. Dermatol. 139, 13–16 (2019).

    Article  CAS  PubMed  Google Scholar 

  61. Guet-Revillet, H. et al. The microbiological landscape of anaerobic infections in hidradenitis suppurativa: a prospective metagenomic study. Clin. Infect. Dis. 65, 282–291 (2017). This paper investigates intracutaneous bacterial colonization in patients with HS and shows the enrichment of specific Gram-negative anaerobic species in chronic HS lesions.

    Article  CAS  PubMed  Google Scholar 

  62. Nikolakis, G. et al. Bacteriology of hidradenitis suppurativa/acne inversa: a review. J. Am. Acad. Dermatol. 73, S12–S18 (2015).

    Article  PubMed  Google Scholar 

  63. Ring, H. C. et al. The bacteriology of hidradenitis suppurativa: a systematic review. Exp. Dermatol. 24, 727–731 (2015).

    Article  CAS  PubMed  Google Scholar 

  64. Kathju, S., Lasko, L. A. & Stoodley, P. Considering hidradenitis suppurativa as a bacterial biofilm disease. FEMS Immunol. Med. Microbiol. 65, 385–389 (2012).

    Article  CAS  PubMed  Google Scholar 

  65. Ring, H. C. et al. Bacterial biofilm in chronic lesions of hidradenitis suppurativa. Br. J. Dermatol. 176, 993–1000 (2017).

    Article  CAS  PubMed  Google Scholar 

  66. Ring, H. C. et al. Normal skin microbiota is altered in pre-clinical hidradenitis suppurativa. Acta Derm. Venereol. 97, 208–213 (2017).

    Article  CAS  PubMed  Google Scholar 

  67. De Vita, V. & Fabbrocini, G. Mechanical stress as a cause of hidradenitis suppurativa: a lesson from a patient with a monster hernia. Acta Dermatovenerol. Croat. 26, 260–261 (2018).

    PubMed  Google Scholar 

  68. Yu, C. C. & Cook, M. G. Hidradenitis suppurativa: a disease of follicular epithelium, rather than apocrine glands. Br. J. Dermatol. 122, 763–769 (1990). This paper describes an early histopathological study that suggests that HS develops upon dilatation and rupture of hair follicles.

    Article  CAS  PubMed  Google Scholar 

  69. Attanoos, R. L., Appleton, M. A. & Douglas-Jones, A. G. The pathogenesis of hidradenitis suppurativa: a closer look at apocrine and apoeccrine glands. Br. J. Dermatol. 133, 254–258 (1995).

    Article  CAS  PubMed  Google Scholar 

  70. Boer, J. & Weltevreden, E. F. Hidradenitis suppurativa or acne inversa. A clinicopathological study of early lesions. Br. J. Dermatol. 135, 721–725 (1996).

    Article  CAS  PubMed  Google Scholar 

  71. Jemec, G. B. & Hansen, U. Histology of hidradenitis suppurativa. J. Am. Acad. Dermatol. 34, 994–999 (1996).

    Article  CAS  PubMed  Google Scholar 

  72. von Laffert, M. et al. Hidradenitis suppurativa (acne inversa): early inflammatory events at terminal follicles and at interfollicular epidermis. Exp. Dermatol. 19, 533–537 (2010).

    Article  Google Scholar 

  73. van der Zee, H. H. et al. Elevated levels of tumour necrosis factor (TNF)-alpha, interleukin (IL)-1beta and IL-10 in hidradenitis suppurativa skin: a rationale for targeting TNF-alpha and IL-1beta. Br. J. Dermatol. 164, 1292–1298 (2011).

    Article  PubMed  CAS  Google Scholar 

  74. Hunger, R. E., Surovy, A. M., Hassan, A. S., Braathen, L. R. & Yawalkar, N. Toll-like receptor 2 is highly expressed in lesions of acne inversa and colocalizes with C-type lectin receptor. Br. J. Dermatol. 158, 691–697 (2008).

    Article  CAS  PubMed  Google Scholar 

  75. Witte-Handel, E. et al. The IL-1 pathway is hyperactive in hidradenitis suppurativa and contributes to skin infiltration and destruction. J. Invest. Dermatol. 139, 1294–1305 (2019). This paper elucidates the role of IL-1β in cutaneous purulence and tissue destruction by transcriptome analyses, stimulation studies with skin-derived cells and ex vivo cytokine neutralization of HS skin.

    Article  PubMed  CAS  Google Scholar 

  76. Kelly, G. et al. Dysregulated cytokine expression in lesional and nonlesional skin in hidradenitis suppurativa. Br. J. Dermatol. 173, 1431–1439 (2015).

    Article  CAS  PubMed  Google Scholar 

  77. Manfredini, M. et al. The P2X7 receptor is overexpressed in the lesional skin of subjects affected by hidradenitis suppurativa: a preliminary study. Dermatology https://doi.org/10.1159/000502026 (2019).

    Article  PubMed  Google Scholar 

  78. Dinarello, C. A., Simon, A. & van der Meer, J. W. Treating inflammation by blocking interleukin-1 in a broad spectrum of diseases. Nat. Rev. Drug. Discov. 11, 633–652 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Sedger, L. M. & McDermott, M. F. TNF and TNF-receptors: from mediators of cell death and inflammation to therapeutic giants — past, present and future. Cytokine Growth Factor. Rev. 25, 453–472 (2014).

    Article  CAS  PubMed  Google Scholar 

  80. Wolk, K. et al. IL-22 and IL-20 are key mediators of the epidermal alterations in psoriasis while IL-17 and IFN-gamma are not. J. Mol. Med. 87, 523–536 (2009).

    Article  CAS  PubMed  Google Scholar 

  81. Kimball, A. B. et al. Two phase 3 trials of adalimumab for hidradenitis suppurativa. N. Engl. J. Med. 375, 422–434 (2016). This paper describes the first large RCT in HS.

    Article  CAS  PubMed  Google Scholar 

  82. van der Zee, H. H. et al. Alterations in leucocyte subsets and histomorphology in normal-appearing perilesional skin and early and chronic hidradenitis suppurativa lesions. Br. J. Dermatol. 166, 98–106 (2012). This paper is the first study presenting immunostaining data demonstrating that keratin fibres act as foreign body material in the skin of patients with HS.

    Article  PubMed  Google Scholar 

  83. List, E. K., Pascual, J. C., Zarchi, K., Nurnberg, B. M. & Jemec, G. B. E. Mast cells in hidradenitis suppurativa: a clinicopathological study. Arch. Dermatol. Res. 311, 331–335 (2019).

    Article  PubMed  Google Scholar 

  84. Platzer, C. et al. Cyclic adenosine monophosphate-responsive elements are involved in the transcriptional activation of the human IL-10 gene in monocytic cells. Eur. J. Immunol. 29, 3098–3104 (1999).

    Article  CAS  PubMed  Google Scholar 

  85. Platzer, C., Meisel, C., Vogt, K., Platzer, M. & Volk, H. D. Up-regulation of monocytic IL-10 by tumor necrosis factor-alpha and cAMP elevating drugs. Int. Immunol. 7, 517–523 (1995).

    Article  CAS  PubMed  Google Scholar 

  86. Sabat, R. et al. Biology of interleukin-10. Cytokine Growth Factor. Rev. 21, 331–344 (2010).

    Article  CAS  PubMed  Google Scholar 

  87. Fiorentino, D. F. et al. IL-10 acts on the antigen-presenting cell to inhibit cytokine production by Th1 cells. J. Immunol. 146, 3444–3451 (1991).

    CAS  PubMed  Google Scholar 

  88. Wolk, K., Docke, W., von Baehr, V., Volk, H. & Sabat, R. Comparison of monocyte functions after LPS- or IL-10-induced reorientation: importance in clinical immunoparalysis. Pathobiology 67, 253–256 (1999).

    Article  CAS  PubMed  Google Scholar 

  89. Hotz, C. et al. Intrinsic defect in keratinocyte function leads to inflammation in hidradenitis suppurativa. J. Invest. Dermatol. 136, 1768–1780 (2016).

    Article  CAS  PubMed  Google Scholar 

  90. Moran, B. et al. Hidradenitis suppurativa is characterized by dysregulation of the Th17:Treg cell axis, which is corrected by anti-TNF therapy. J. Invest. Dermatol. 137, 2389–2395 (2017). This paper uses multi-colour flow cytometry to investigate the cytokine production capacity of T cells derived from lesional and perilesional skin compared with unaffected HS skin. The results show the enrichment of CD4 + T cells that simultaneously secret multiple cytokines, especially in perilesional skin.

    Article  CAS  PubMed  Google Scholar 

  91. Sabat, R., Wolk, K., Loyal, L., Docke, W. D. & Ghoreschi, K. T cell pathology in skin inflammation. Semin. Immunopathol. 41, 359–377 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  92. Schroder, K., Hertzog, P. J., Ravasi, T. & Hume, D. A. Interferon-gamma: an overview of signals, mechanisms and functions. J. Leukoc. Biol. 75, 163–189 (2004).

    Article  CAS  PubMed  Google Scholar 

  93. Van Raemdonck, K., Van den Steen, P. E., Liekens, S., Van Damme, J. & Struyf, S. CXCR3 ligands in disease and therapy. Cytokine Growth Factor. Rev. 26, 311–327 (2015).

    Article  PubMed  CAS  Google Scholar 

  94. Vossen, A. et al. Novel cytokine and chemokine markers of hidradenitis suppurativa reflect chronic inflammation and itch. Allergy 74, 631–634 (2019).

    PubMed  Google Scholar 

  95. Kao, C. Y. et al. IL-17 markedly up-regulates beta-defensin-2 expression in human airway epithelium via JAK and NF-kappaB signaling pathways. J. Immunol. 173, 3482–3491 (2004).

    Article  CAS  PubMed  Google Scholar 

  96. Albanesi, C., Cavani, A. & Girolomoni, G. IL-17 is produced by nickel-specific T lymphocytes and regulates ICAM-1 expression and chemokine production in human keratinocytes: synergistic or antagonist effects with IFN-gamma and TNF-alpha. J. Immunol. 162, 494–502 (1999).

    CAS  PubMed  Google Scholar 

  97. Fossiez, F. et al. T cell interleukin-17 induces stromal cells to produce proinflammatory and hematopoietic cytokines. J. Exp. Med. 183, 2593–2603 (1996).

    Article  CAS  PubMed  Google Scholar 

  98. Wolk, K. et al. The Th17 cytokine IL-22 induces IL-20 production in keratinocytes: a novel immunological cascade with potential relevance in psoriasis. Eur. J. Immunol. 39, 3570–3581 (2009).

    Article  CAS  PubMed  Google Scholar 

  99. Witte, E. et al. IL-19 is a component of the pathogenetic IL-23/IL-17 cascade in psoriasis. J. Invest. Dermatol. 134, 2757–2767 (2014).

    Article  CAS  PubMed  Google Scholar 

  100. Liang, S. C. et al. Interleukin (IL)-22 and IL-17 are coexpressed by Th17 cells and cooperatively enhance expression of antimicrobial peptides. J. Exp. Med. 203, 2271–2279 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  101. Shen, F., Ruddy, M. J., Plamondon, P. & Gaffen, S. L. Cytokines link osteoblasts and inflammation: microarray analysis of interleukin-17- and TNF-alpha-induced genes in bone cells. J. Leukoc. Biol. 77, 388–399 (2005).

    Article  CAS  PubMed  Google Scholar 

  102. Weiss, B. et al. Cloning of murine IL-22 receptor alpha 2 and comparison with its human counterpart. Genes Immun. 5, 330–336 (2004).

    Article  CAS  PubMed  Google Scholar 

  103. Sabat, R., Ouyang, W. & Wolk, K. Therapeutic opportunities of the IL-22-IL-22R1 system. Nat. Rev. Drug. Discov. 13, 21–38 (2014).

    Article  CAS  PubMed  Google Scholar 

  104. Mozeika, E., Pilmane, M., Nurnberg, B. M. & Jemec, G. B. Tumour necrosis factor-alpha and matrix metalloproteinase-2 are expressed strongly in hidradenitis suppurativa. Acta Derm. Venereol. 93, 301–304 (2013).

    Article  PubMed  CAS  Google Scholar 

  105. Radaeva, S., Sun, R., Pan, H. N., Hong, F. & Gao, B. Interleukin 22 (IL-22) plays a protective role in T cell-mediated murine hepatitis: IL-22 is a survival factor for hepatocytes via STAT3 activation. Hepatology 39, 1332–1342 (2004).

    Article  CAS  PubMed  Google Scholar 

  106. Gimblet, C. et al. IL-22 protects against tissue damage during cutaneous leishmaniasis. PLoS One 10, e0134698 (2015).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  107. Chestovich, P. J. et al. Interleukin-22: implications for liver ischemia-reperfusion injury. Transplantation 93, 485–492 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  108. Sabat, R. & Wolk, K. Deciphering the role of interleukin-22 in metabolic alterations. Cell Biosci. 5, 68 (2015).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  109. Wang, X. et al. Interleukin-22 alleviates metabolic disorders and restores mucosal immunity in diabetes. Nature 514, 237–241 (2014).

    Article  CAS  PubMed  Google Scholar 

  110. Danby, F. W., Jemec, G. B., Marsch, W. & von Laffert, M. Preliminary findings suggest hidradenitis suppurativa may be due to defective follicular support. Br. J. Dermatol. 168, 1034–1039 (2013).

    Article  CAS  PubMed  Google Scholar 

  111. Greb, J. E. et al. Psoriasis. Nat. Rev. Dis. Prim. 2, 16082 (2016).

    Article  PubMed  Google Scholar 

  112. Thomi, R. et al. Interleukin-32 is highly expressed in lesions of hidradenitis suppurativa. Br. J. Dermatol. 177, 1358–1366 (2017).

    Article  CAS  PubMed  Google Scholar 

  113. Thomi, R., Kakeda, M., Yawalkar, N., Schlapbach, C. & Hunger, R. E. Increased expression of the interleukin-36 cytokines in lesions of hidradenitis suppurativa. J. Eur. Acad. Dermatol. Venereol. 31, 2091–2096 (2017).

    Article  CAS  PubMed  Google Scholar 

  114. Di Caprio, R. et al. IL-36 cytokines are increased in acne and hidradenitis suppurativa. Arch. Dermatol. Res. 309, 673–678 (2017).

    Article  PubMed  CAS  Google Scholar 

  115. Hessam, S. et al. Interleukin-36 in hidradenitis suppurativa: evidence for a distinctive proinflammatory role and a key factor in the development of an inflammatory loop. Br. J. Dermatol. 178, 761–767 (2018).

    Article  CAS  PubMed  Google Scholar 

  116. Foster, A. M. et al. IL-36 promotes myeloid cell infiltration, activation, and inflammatory activity in skin. J. Immunol. 192, 6053–6061 (2014).

    Article  CAS  PubMed  Google Scholar 

  117. Winkle, S. M., Throop, A. L. & Herbst-Kralovetz, M. M. IL-36gamma augments host defense and immune responses in human female reproductive tract epithelial cells. Front. Microbiol. 7, 955 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  118. Wolk, K. et al. Lipocalin-2 is expressed by activated granulocytes and keratinocytes in affected skin and reflects disease activity in acne inversa/hidradenitis suppurativa. Br. J. Dermatol. 177, 1385–1393 (2017).

    Article  CAS  PubMed  Google Scholar 

  119. Abella, V. et al. The potential of lipocalin-2/NGAL as biomarker for inflammatory and metabolic diseases. Biomarkers 20, 565–571 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  120. Chakraborty, S., Kaur, S., Guha, S. & Batra, S. K. The multifaceted roles of neutrophil gelatinase associated lipocalin (NGAL) in inflammation and cancer. Biochim. Biophys. Acta 1826, 129–169 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  121. Thomi, R. et al. Elevated levels of the antimicrobial peptide LL-37 in hidradenitis suppurativa are associated with a Th1/Th17 immune response. Exp. Dermatol. 27, 172–177 (2018).

    Article  CAS  PubMed  Google Scholar 

  122. von Laffert, M., Stadie, V., Wohlrab, J. & Marsch, W. C. Hidradenitis suppurativa/acne inversa: bilocated epithelial hyperplasia with very different sequelae. Br. J. Dermatol. 164, 367–371 (2011).

    Article  Google Scholar 

  123. Jimenez-Gallo, D. et al. The clinical significance of increased serum proinflammatory cytokines, C-reactive protein, and erythrocyte sedimentation rate in patients with hidradenitis suppurativa. Mediators Inflamm. 2017, 2450401 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  124. Wolk, K. & Sabat, R. Adipokines in psoriasis: an important link between skin inflammation and metabolic alterations. Rev. Endocr. Metab. Disord. 17, 305–317 (2016).

    Article  CAS  PubMed  Google Scholar 

  125. Malara, A. et al. Adipokines are dysregulated in patients with hidradenitis suppurativa. Br. J. Dermatol. 178, 792–793 (2018).

    Article  CAS  PubMed  Google Scholar 

  126. Girouard, S. D., Falk, R. H., Rennke, H. G. & Merola, J. F. Hidradenitis suppurativa resulting in systemic amyloid A amyloidosis: a case report and review of the literature. Dermatol. Online J. 18, 2 (2012).

    PubMed  Google Scholar 

  127. Schandorff, K. D., Miller, I. M., Krustrup, D., Jemec, G. B. & Marckmann, P. Renal amyloid A amyloidosis as a complication of hidradenitis suppurativa. Clin. Nephrol. 86, 51–54 (2016).

    Article  CAS  PubMed  Google Scholar 

  128. Damen, M., Popa, C. D., Netea, M. G., Dinarello, C. A. & Joosten, L. A. B. Interleukin-32 in chronic inflammatory conditions is associated with a higher risk of cardiovascular diseases. Atherosclerosis 264, 83–91 (2017).

    Article  CAS  PubMed  Google Scholar 

  129. Tsaousi, A. et al. MMP8 is increased in lesions and blood of acne inversa patients: a potential link to skin destruction and metabolic alterations. Mediators Inflamm. 2016, 4097574 (2016).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  130. Matusiak, L., Bieniek, A. & Szepietowski, J. C. Increased serum tumour necrosis factor-alpha in hidradenitis suppurativa patients: is there a basis for treatment with anti-tumour necrosis factor-alpha agents? Acta Derm. Venereol. 89, 601–603 (2009).

    Article  CAS  PubMed  Google Scholar 

  131. Matusiak, L., Szczech, J., Bieniek, A., Nowicka-Suszko, D. & Szepietowski, J. C. Increased interleukin (IL)-17 serum levels in patients with hidradenitis suppurativa: implications for treatment with anti-IL-17 agents. J. Am. Acad. Dermatol. 76, 670–675 (2017).

    Article  CAS  PubMed  Google Scholar 

  132. Armaka, M. et al. Mesenchymal cell targeting by TNF as a common pathogenic principle in chronic inflammatory joint and intestinal diseases. J. Exp. Med. 205, 331–337 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  133. Uluckan, O. et al. Chronic skin inflammation leads to bone loss by IL-17-mediated inhibition of Wnt signaling in osteoblasts. Sci. Transl. Med. 8, 330ra337 (2016).

    Article  CAS  Google Scholar 

  134. Freysz, M., Jemec, G. B. & Lipsker, D. A systematic review of terms used to describe hidradenitis suppurativa. Br. J. Dermatol. 173, 1298–1300 (2015).

    Article  CAS  PubMed  Google Scholar 

  135. Revuz, J. Hidradenitis suppurativa. J. Eur. Acad. Dermatol. Venereol. 23, 985–998 (2009).

    Article  CAS  PubMed  Google Scholar 

  136. Schrader, A. M., Deckers, I. E., van der Zee, H. H., Boer, J. & Prens, E. P. Hidradenitis suppurativa: a retrospective study of 846 Dutch patients to identify factors associated with disease severity. J. Am. Acad. Dermatol. 71, 460–467 (2014). This paper reports on risk factors in a large representative cohort of patients with HS.

    Article  PubMed  Google Scholar 

  137. Saunte, D. M. et al. Diagnostic delay in hidradenitis suppurativa is a global problem. Br. J. Dermatol. 173, 1546–1549 (2015).

    Article  CAS  PubMed  Google Scholar 

  138. Wortsman, X., Castro, A. & Figueroa, A. Color Doppler ultrasound assessment of morphology and types of fistulous tracts in hidradenitis suppurativa (HS). J. Am. Acad. Dermatol. 75, 760–767 (2016).

    Article  PubMed  Google Scholar 

  139. Wortsman, X. et al. Ultrasound in-depth characterization and staging of hidradenitis suppurativa. Dermatol. Surg. 39, 1835–1842 (2013).

    Article  CAS  PubMed  Google Scholar 

  140. Virgilio, E., Bocchetti, T. & Balducci, G. Utility of MRI in the diagnosis and post-treatment evaluation of anogenital hidradenitis suppurativa. Dermatol. Surg. 41, 865–866 (2015).

    Article  CAS  PubMed  Google Scholar 

  141. Hurley, H. in Dermatologic Surgery: Principles and Practice (eds Roenigk, R. K., Roenigk, H. H. Jr). 729–739 (CRC Press, 1989).

  142. Sartorius, K., Emtestam, L., Jemec, G. B. & Lapins, J. Objective scoring of hidradenitis suppurativa reflecting the role of tobacco smoking and obesity. Br. J. Dermatol. 161, 831–839 (2009).

    Article  CAS  PubMed  Google Scholar 

  143. Kimball, A. B. et al. Adalimumab for the treatment of moderate to severe hidradenitis suppurativa: a parallel randomized trial. Ann. Intern. Med. 157, 846–855 (2012).

    Article  PubMed  Google Scholar 

  144. Hessam, S. et al. A novel severity assessment scoring system for hidradenitis suppurativa. JAMA Dermatol. 154, 330–335 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  145. Kokolakis, G. & Sabat, R. Distinguishing mild, moderate, and severe hidradenitis suppurativa. JAMA Dermatol. 154, 971–972 (2018).

    Article  PubMed  Google Scholar 

  146. Horvath, B. et al. Hurley staging refined: a proposal by the Dutch Hidradenitis Suppurativa Expert Group. Acta Derm. Venereol. 97, 412–413 (2017).

    Article  PubMed  Google Scholar 

  147. Chernyshov, P. V. The evolution of quality of life assessment and use in dermatology. Dermatology 235, 167–174 (2019).

    Article  PubMed  Google Scholar 

  148. Ferreira-Valente, M. A., Pais-Ribeiro, J. L. & Jensen, M. P. Validity of four pain intensity rating scales. Pain 152, 2399–2404 (2011).

    Article  PubMed  Google Scholar 

  149. Kimball, A. B. et al. Psychometric properties of the itch numeric rating scale in patients with moderate-to-severe plaque psoriasis. Br. J. Dermatol. 175, 157–162 (2016).

    Article  CAS  PubMed  Google Scholar 

  150. Pedersen, C. B. et al. Reliability and validity of the psoriasis itch visual analog scale in psoriasis vulgaris. J. Dermatol. Treat. 28, 213–220 (2017).

    Article  Google Scholar 

  151. Spinhoven, P. et al. A validation study of the Hospital Anxiety and Depression Scale (HADS) in different groups of Dutch subjects. Psychol. Med. 27, 363–370 (1997).

    Article  CAS  PubMed  Google Scholar 

  152. Yao, Y., Jorgensen, A. R. & Thomsen, S. F. Work productivity and activity impairment in patients with hidradenitis suppurativa: a cross-sectional study. Int. J. Dermatol. 59, 333–340 (2019).

    Article  PubMed  Google Scholar 

  153. Wieland, C. W. et al. Myeloid marker S100A8/A9 and lymphocyte marker, soluble interleukin 2 receptor: biomarkers of hidradenitis suppurativa disease activity? Br. J. Dermatol. 168, 1252–1258 (2013).

    Article  CAS  PubMed  Google Scholar 

  154. Matusiak, L., Salomon, J., Nowicka-Suszko, D., Bieniek, A. & Szepietowski, J. C. Chitinase-3-like protein 1 (YKL-40): novel biomarker of hidradenitis suppurativa disease activity? Acta Derm. Venereol. 95, 736–737 (2015).

    Article  CAS  PubMed  Google Scholar 

  155. Grant, A., Gonzalez, T., Montgomery, M. O., Cardenas, V. & Kerdel, F. A. Infliximab therapy for patients with moderate to severe hidradenitis suppurativa: a randomized, double-blind, placebo-controlled crossover trial. J. Am. Acad. Dermatol. 62, 205–217 (2010).

    Article  CAS  PubMed  Google Scholar 

  156. Gold, D. A., Reeder, V. J., Mahan, M. G. & Hamzavi, I. H. The prevalence of metabolic syndrome in patients with hidradenitis suppurativa. J. Am. Acad. Dermatol. 70, 699–703 (2014).

    Article  PubMed  Google Scholar 

  157. Ng, S. C. et al. Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies. Lancet 390, 2769–2778 (2018).

    Article  Google Scholar 

  158. van der Zee, H. H., de Winter, K., van der Woude, C. J. & Prens, E. P. The prevalence of hidradenitis suppurativa in 1093 patients with inflammatory bowel disease. Br. J. Dermatol. 171, 673–675 (2014).

    Article  PubMed  Google Scholar 

  159. Deckers, I. E., van der Zee, H. H. & Prens, E. P. Severe fatigue based on anaemia in patients with hidradenitis suppurativa: report of two cases and a review of the literature. J. Eur. Acad. Dermatol. Venereol. 30, 174–175 (2016).

    Article  CAS  PubMed  Google Scholar 

  160. Fraenkel, P. G. Anemia of inflammation: a review. Med. Clin. North. Am. 101, 285–296 (2017).

    Article  PubMed  Google Scholar 

  161. Cugno, M., Borghi, A. & Marzano, A. V. PAPA, PASH and PAPASH syndromes: pathophysiology, presentation and treatment. Am. J. Clin. Dermatol. 18, 555–562 (2017).

    Article  PubMed  Google Scholar 

  162. Vanlaerhoven, A. et al. Hurley III hidradenitis suppurativa has an aggressive disease course. Dermatology 234, 232–233 (2018).

    Article  PubMed  Google Scholar 

  163. Kromann, C. B., Ibler, K. S., Kristiansen, V. B. & Jemec, G. B. The influence of body weight on the prevalence and severity of hidradenitis suppurativa. Acta Derm. Venereol. 94, 553–557 (2014).

    Article  PubMed  Google Scholar 

  164. Micieli, R. & Alavi, A. Lymphedema in patients with hidradenitis suppurativa: a systematic review of published literature. Int. J. Dermatol. 57, 1471–1480 (2018).

    Article  PubMed  Google Scholar 

  165. Russ, E. & Castillo, M. Lumbosacral epidural abscess due to hidradenitis suppurativa. AJR Am. J. Roentgenol. 178, 770–771 (2002).

    Article  PubMed  Google Scholar 

  166. Chapman, S., Delgadillo, D. III, Barber, C. & Khachemoune, A. Cutaneous squamous cell carcinoma complicating hidradenitis suppurativa: a review of the prevalence, pathogenesis, and treatment of this dreaded complication. Acta Dermatovenerol. Alp. Pannonica Adriat. 27, 25–28 (2018).

    PubMed  Google Scholar 

  167. Tannenbaum, R., Strunk, A. & Garg, A. Association between hidradenitis suppurativa and lymphoma. JAMA Dermatol. 155, 624–625 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  168. Wortsman, X. Imaging of hidradenitis suppurativa. Dermatol. Clin. 34, 59–68 (2016).

    Article  CAS  PubMed  Google Scholar 

  169. Sivanand, A., Gulliver, W. P., Josan, C. K., Alhusayen, R. & Fleming, P. J. Weight loss and dietary interventions for hidradenitis suppurativa: a systematic review. J. Cutan. Med. Surg. 24, 64–72 (2019).

    Article  PubMed  Google Scholar 

  170. Loh, T. Y., Hendricks, A. J., Hsiao, J. L. & Shi, V. Y. Undergarment and fabric selection in the management of hidradenitis suppurativa. Dermatology https://doi.org/10.1159/000501611 (2019).

    Article  PubMed  Google Scholar 

  171. Hunger, R. E. et al. Swiss practice recommendations for the management of hidradenitis suppurativa/acne inversa. Dermatology 233, 113–119 (2017).

    Article  CAS  PubMed  Google Scholar 

  172. Megna, M. et al. Hidradenitis suppurativa: guidelines of the Italian society of dermatology and venereology (SIDeMaST) for the use of anti-TNF-α agents. G. Ital. Dermatol. Venereol. 150, 731–739 (2015).

    CAS  PubMed  Google Scholar 

  173. Zouboulis, C. C. et al. S1 guideline for the treatment of hidradenitis suppurativa/acne inversa * (number ICD-10 L73.2) [German]. J. Dtsch. Dermatol. Ges. 10, S1–S31 (2012).

    Article  PubMed  Google Scholar 

  174. Zouboulis, C. C. et al. European S1 guideline for the treatment of hidradenitis suppurativa/acne inversa. J. Eur. Acad. Dermatol. Venereol. 29, 619–644 (2015).

    Article  CAS  PubMed  Google Scholar 

  175. Sabat, R. et al. Acne inversa/hidradenitis suppurativa: an update. Hautarzt 68, 999–1006 (2017).

    Article  CAS  PubMed  Google Scholar 

  176. Dauden, E. et al. Recommendations for the management of comorbidity in hidradenitis suppurativa. J. Eur. Acad. Dermatol. Venereol. 32, 129–144 (2018).

    Article  CAS  PubMed  Google Scholar 

  177. Nielsen, R. M., Lindso Andersen, P., Sigsgaard, V., Theut Riis, P. & Jemec, G. B. Pain perception in patients with hidradenitis suppurativa. Br. J. Dermatol. 182, 166–174 (2019).

    PubMed  Google Scholar 

  178. WHO. Scoping document for WHO guidelines for the pharmacological treatment of persisting pain in adults with medical illnesses. https://www.who.int/medicines/areas/quality_safety/Scoping_WHO_GLs_PersistPainAdults_webversion.pdf?ua=1 (2012).

  179. Clemmensen, O. J. Topical treatment of hidradenitis suppurativa with clindamycin. Int. J. Dermatol. 22, 325–328 (1983).

    Article  CAS  PubMed  Google Scholar 

  180. Fischer, A. H., Haskin, A. & Okoye, G. A. Patterns of antimicrobial resistance in lesions of hidradenitis suppurativa. J. Am. Acad. Dermatol. 76, 309–313 (2017).

    Article  CAS  PubMed  Google Scholar 

  181. Jemec, G. B. & Wendelboe, P. Topical clindamycin versus systemic tetracycline in the treatment of hidradenitis suppurativa. J. Am. Acad. Dermatol. 39, 971–974 (1998).

    Article  CAS  PubMed  Google Scholar 

  182. Matusiak, L., Bieniek, A. & Szepietowski, J. C. Bacteriology of hidradenitis suppurativa — which antibiotics are the treatment of choice? Acta Derm. Venereol. 94, 699–702 (2014).

    Article  PubMed  Google Scholar 

  183. Scheinfeld, N. Hidradenitis suppurativa: a practical review of possible medical treatments based on over 350 hidradenitis patients. Dermatol. Online J. 19, 1 (2013).

    PubMed  Google Scholar 

  184. Mendonca, C. O. & Griffiths, C. E. Clindamycin and rifampicin combination therapy for hidradenitis suppurativa. Br. J. Dermatol. 154, 977–978 (2006).

    Article  CAS  PubMed  Google Scholar 

  185. Bettoli, V., Join-Lambert, O. & Nassif, A. Antibiotic treatment of hidradenitis suppurativa. Dermatol. Clin. 34, 81–89 (2016).

    Article  CAS  PubMed  Google Scholar 

  186. Join-Lambert, O. et al. Dramatic reduction of clindamycin plasma concentration in hidradenitis suppurativa patients treated with the rifampin-clindamycin combination. Eur. J. Dermatol. 24, 94–95 (2014).

    Article  CAS  PubMed  Google Scholar 

  187. Albrecht, J., Baine, P. A., Ladizinski, B., Jemec, G. B. & Bigby, M. Long-term clinical safety of clindamycin and rifampicin combination for the treatment of hidradenitis suppurativa. A critically appraised topic. Br. J. Dermatol. 180, 749–755 (2019).

    Article  CAS  PubMed  Google Scholar 

  188. Join-Lambert, O. et al. Efficacy of ertapenem in severe hidradenitis suppurativa: a pilot study in a cohort of 30 consecutive patients. J. Antimicrob. Chemother. 71, 513–520 (2016).

    Article  CAS  PubMed  Google Scholar 

  189. Join-Lambert, O. et al. Efficacy of rifampin-moxifloxacin-metronidazole combination therapy in hidradenitis suppurativa. Dermatology 222, 49–58 (2011).

    Article  CAS  PubMed  Google Scholar 

  190. Yazdanyar, S., Boer, J., Ingvarsson, G., Szepietowski, J. C. & Jemec, G. B. Dapsone therapy for hidradenitis suppurativa: a series of 24 patients. Dermatology 222, 342–346 (2011).

    Article  CAS  PubMed  Google Scholar 

  191. Riis, P. T. et al. Intralesional triamcinolone for flares of hidradenitis suppurativa (HS): a case series. J. Am. Acad. Dermatol. 75, 1151–1155 (2016).

    Article  CAS  PubMed  Google Scholar 

  192. Kimball, A. B. et al. HiSCR (Hidradenitis Suppurativa Clinical Response): a novel clinical endpoint to evaluate therapeutic outcomes in patients with hidradenitis suppurativa from the placebo-controlled portion of a phase 2 adalimumab study. J. Eur. Acad. Dermatol. Venereol. 30, 989–994 (2016).

    Article  CAS  PubMed  Google Scholar 

  193. Kimball, A. B., Ganguli, A. & Fleischer, A. Reliability of the hidradenitis suppurativa clinical response in the assessment of patients with hidradenitis suppurativa. J. Eur. Acad. Dermatol. Venereol. 32, 2254–2256 (2018).

    Article  CAS  PubMed  Google Scholar 

  194. Zouboulis, C. C. et al. Long-term adalimumab efficacy in patients with moderate-to-severe hidradenitis suppurativa/acne inversa: 3-year results of a phase 3 open-label extension study. J. Am. Acad. Dermatol. 80, 60–69 e62 (2019).

    Article  CAS  PubMed  Google Scholar 

  195. Tzanetakou, V. et al. Safety and efficacy of anakinra in severe hidradenitis suppurativa: a randomized clinical trial. JAMA Dermatol. 152, 52–59 (2016).

    Article  PubMed  Google Scholar 

  196. Maarouf, M., Clark, A. K., Lee, D. E. & Shi, V. Y. Targeted treatments for hidradenitis suppurativa: a review of the current literature and ongoing clinical trials. J. Dermatol. Treat. 29, 441–449 (2018).

    Article  Google Scholar 

  197. Kanni, T. et al. MABp1 targeting IL-1α for moderate to severe hidradenitis suppurativa not eligible for adalimumab: a randomized study. J. Invest. Dermatol. 138, 795–801 (2018).

    Article  CAS  PubMed  Google Scholar 

  198. Weber, P., Seyed Jafari, S. M., Yawalkar, N. & Hunger, R. E. Apremilast in the treatment of moderate to severe hidradenitis suppurativa: a case series of 9 patients. J. Am. Acad. Dermatol. 76, 1189–1191 (2017).

    Article  PubMed  Google Scholar 

  199. Kerdel, F. R. et al. Apremilast for the treatment of mild-to-moderate hidradenitis suppurativa in a prospective, open-label, phase 2 study. J. Drugs Dermatol. 18, 170–176 (2019).

    PubMed  Google Scholar 

  200. Vossen, A., van Doorn, M. B. A., van der Zee, H. H. & Prens, E. P. Apremilast for moderate hidradenitis suppurativa: results of a randomized controlled trial. J. Am. Acad. Dermatol. 80, 80–88 (2019).

    Article  CAS  PubMed  Google Scholar 

  201. van der Zee, H. H., Prens, E. P. & Boer, J. Deroofing: a tissue-saving surgical technique for the treatment of mild to moderate hidradenitis suppurativa lesions. J. Am. Acad. Dermatol. 63, 475–480 (2010). This paper introduces a practical surgical technique of great clinical use in the management of HS.

    Article  PubMed  Google Scholar 

  202. Lapins, J., Marcusson, J. A. & Emtestam, L. Surgical treatment of chronic hidradenitis suppurativa: CO2 laser stripping-secondary intention technique. Br. J. Dermatol. 131, 551–556 (1994). This paper gives detailed insight into a useful management technique for HS of intermediate severity.

    Article  CAS  PubMed  Google Scholar 

  203. Blok, J. L., Spoo, J. R., Leeman, F. W., Jonkman, M. F. & Horvath, B. Skin-Tissue-sparing Excision with Electrosurgical Peeling (STEEP): a surgical treatment option for severe hidradenitis suppurativa Hurley stage II/III. J. Eur. Acad. Dermatol. Venereol. 29, 379–382 (2015).

    Article  CAS  PubMed  Google Scholar 

  204. Janse, I., Bieniek, A., Horvath, B. & Matusiak, L. Surgical procedures in hidradenitis suppurativa. Dermatol. Clin. 34, 97–109 (2016).

    Article  CAS  PubMed  Google Scholar 

  205. Morgan, W. P., Harding, K. G. & Hughes, L. E. A comparison of skin grafting and healing by granulation, following axillary excision for hidradenitis suppurativa. Ann. R. Coll. Surg. Engl. 65, 235–236 (1983).

    CAS  PubMed  PubMed Central  Google Scholar 

  206. Tierney, E., Mahmoud, B. H., Hexsel, C., Ozog, D. & Hamzavi, I. Randomized control trial for the treatment of hidradenitis suppurativa with a neodymium-doped yttrium aluminium garnet laser. Dermatol. Surg. 35, 1188–1198 (2009). This paper describes the utility of Nd:YAG treatment in HS.

    Article  CAS  PubMed  Google Scholar 

  207. Saunte, D. M. & Lapins, J. Lasers and intense pulsed light hidradenitis suppurativa. Dermatol. Clin. 34, 111–119 (2016).

    Article  CAS  PubMed  Google Scholar 

  208. Matusiak, L., Bieniek, A. & Szepietowski, J. C. Psychophysical aspects of hidradenitis suppurativa. Acta Derm. Venereol. 90, 264–268 (2010).

    Article  PubMed  Google Scholar 

  209. von der Werth, J. M. & Jemec, G. B. Morbidity in patients with hidradenitis suppurativa. Br. J. Dermatol. 144, 809–813 (2001). This paper describes a cross-sectional study that broadly demonstrates the health-related quality of life measures and elucidates key factors that make HS more burdensome, emphasizing the important role of health care providers in diminishing disease burden.

    Article  PubMed  Google Scholar 

  210. Onderdijk, A. J. et al. Depression in patients with hidradenitis suppurativa. J. Eur. Acad. Dermatol. Venereol. 27, 473–478 (2013).

    Article  CAS  PubMed  Google Scholar 

  211. Matusiak, L., Szczech, J., Kaaz, K., Lelonek, E. & Szepietowski, J. C. Clinical characteristics of pruritus and pain in patients with hidradenitis suppurativa. Acta Derm. Venereol. 98, 191–194 (2018).

    Article  PubMed  Google Scholar 

  212. Smith, H. S., Chao, J. D. & Teitelbaum, J. Painful hidradenitis suppurativa. Clin. J. Pain. 26, 435–444 (2010).

    Article  PubMed  Google Scholar 

  213. Wolkenstein, P. et al. Quality of life impairment in hidradenitis suppurativa: a study of 61 cases. J. Am. Acad. Dermatol. 56, 621–623 (2007).

    Article  PubMed  Google Scholar 

  214. Kaaz, K., Szepietowski, J. C. & Matusiak, L. Influence of itch and pain on sleep quality in patients with hidradenitis suppurativa. Acta Derm. Venereol. 98, 757–761 (2018).

    Article  PubMed  Google Scholar 

  215. Vossen, A., Schoenmakers, A., van Straalen, K. R., Prens, E. P. & van der Zee, H. H. Assessing pruritus in hidradenitis suppurativa: a cross-sectional study. Am. J. Clin. Dermatol. 18, 687–695 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  216. Kurek, A. et al. Profound disturbances of sexual health in patients with acne inversa. J. Am. Acad. Dermatol. 67, 422–428 (2012).

    Article  PubMed  Google Scholar 

  217. Sampogna, F. et al. Impairment of sexual life in 3,485 dermatological outpatients from a multicentre study in 13 European countries. Acta Derm. Venereol. 97, 478–482 (2017).

    Article  PubMed  Google Scholar 

  218. Jemec, G. B., Heidenheim, M. & Nielsen, N. H. Hidradenitis suppurativa — characteristics and consequences. Clin. Exp. Dermatol. 21, 419–423 (1996).

    Article  CAS  PubMed  Google Scholar 

  219. Machado, M. O. et al. Depression and anxiety in adults with hidradenitis suppurativa: a systematic review and meta-analysis. JAMA Dermatol. https://doi.org/10.1001/jamadermatol.2019.0759 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  220. Thorlacius, L., Cohen, A. D., Gislason, G. H., Jemec, G. B. E. & Egeberg, A. Increased suicide risk in patients with hidradenitis suppurativa. J. Invest. Dermatol. 138, 52–57 (2018). This paper reports on a registry-based study that clearly demonstrates the increased risk of suicide among patients with HS compared with the general population.

    Article  CAS  PubMed  Google Scholar 

  221. Schneider-Burrus, S. et al. Association of hidradenitis suppurativa with body image. JAMA Dermatol. 154, 447–451 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  222. Esmann, S. & Jemec, G. B. Psychosocial impact of hidradenitis suppurativa: a qualitative study. Acta Derm. Venereol. 91, 328–332 (2011).

    Article  PubMed  Google Scholar 

  223. Scala, E. et al. A new Th-17 cytokine in hidradenitis suppurativa: antimicrobial and pro-inflammatory role of IL-26. Br. J. Dermatol. https://doi.org/10.1111/bjd.17854 (2019).

    Article  PubMed  Google Scholar 

  224. Lima, A. L. et al. Keratinocytes and neutrophils are important sources of proinflammatory molecules in hidradenitis suppurativa. Br. J. Dermatol. 174, 514–521 (2016).

    Article  CAS  PubMed  Google Scholar 

  225. Witte, K. et al. Increased presence and differential molecular imprinting of transit amplifying cells in psoriasis. J. Mol. Med. 98, 111–122 (2020).

    Article  CAS  PubMed  Google Scholar 

  226. Ring, H. C. et al. The follicular skin microbiome in patients with hidradenitis suppurativa and healthy controls. JAMA Dermatol. 153, 897–905 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  227. Clark, A. K., Quinonez, R. L., Saric, S. & Sivamani, R. K. Hormonal therapies for hidradenitis suppurativa: review. Dermatol. Online J. 23, 13030/qt6383k0n4 (2017).

    PubMed  Google Scholar 

  228. Golbari, N. M., Porter, M. L. & Kimball, A. B. Antiandrogen therapy with spironolactone for the treatment of hidradenitis suppurativa. J. Am. Acad. Dermatol. 80, 114–119 (2019).

    Article  CAS  PubMed  Google Scholar 

  229. Loget, J. et al. Misdiagnosis of hidradenitis suppurativa continues to be a major issue. The R-ENS Verneuil study. Ann. Dermatol. Venereol. 145, 331–338 (2018).

    Article  CAS  PubMed  Google Scholar 

  230. Canoui-Poitrine, F. et al. Identification of three hidradenitis suppurativa phenotypes: latent class analysis of a cross-sectional study. J. Invest. Dermatol. 133, 1506–1511 (2013).

    Article  CAS  PubMed  Google Scholar 

  231. Kimball, A. B., Sundaram, M., Banderas, B., Foley, C. & Shields, A. L. Development and initial psychometric evaluation of patient-reported outcome questionnaires to evaluate the symptoms and impact of hidradenitis suppurativa. J. Dermatol. Treat. 29, 152–164 (2018).

    Article  Google Scholar 

  232. Thorlacius, L. et al. Towards global consensus on core outcomes for hidradenitis suppurativa research: an update from the HISTORIC consensus meetings I and II. Br. J. Dermatol. 178, 715–721 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  233. Porter, M. L., Golbari, N. M., Lockwood, S. J. & Kimball, A. B. Overview and update on biologic therapy for moderate-to-severe hidradenitis suppurativa. Semin. Cutan. Med. Surg. 37, 182–189 (2018).

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors thank A. Vossen (Erasmus University Medical Center), G. Kokolakis (Charité – Universitätsmedizin Berlin), I. Chlebicka (Wrocław Medical University), K. van Straalen (Erasmus University Medical Center) and J. Triebus (Charité – Universitätsmedizin Berlin) for their help with this manuscript. The authors also acknowledge the support by the German Federal Ministry of Education and Research (http://www.bmbf.de/; grant 01ZX1312A to K.W. and R.S.).

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Authors

Contributions

Introduction (R.S.); Epidemiology (G.B.E.J.); Mechanisms/pathophysiology (K.W.); Diagnosis, screening and prevention (E.P.); Management (G.B.E.J.); Quality of life (Ł.M.); Outlook (A.B.K. and R.S.); Overview of Primer (R.S.). R.S. and G.B.E.J. contributed equally and are co-first authors. E.P. and K.W. contributed equally and are co-last authors.

Corresponding author

Correspondence to Robert Sabat.

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Competing interests

R.S. is a member of Arbeitsgemeinschaft Dermatologische Forschung (ADF; Consortium for Dermatological Research), the German Society of Allergy and Clinical Immunology (DGAKI), the German Society of Immunology (DGfI), the American Association of Immunologists (AAI), the International Psoriasis Council (IPC) and the European Hidradenitis Suppurativa Foundation (EHSF), and is the spokesman of the ADF Psoriasis Group. R.S. has received research grants and scientific awards or honoraria for participation on advisory boards, clinical trials or as speaker for one or more of the following: AbbVie Inc., AbbVie Deutschland GmbH & Co. KG, Bayer Schering Pharma AG, Biogen IDEC GmbH, Boehringer Ingelheim Pharma GmbH & Co. KG, Celgene GmbH, Celgene International II Sàrl, Charité Research Organization GmbH, Dr. Willmar Schwabe GmbH & Co. KG, Flexopharm GmbH & Co. KG, Generon Corporation Ltd., Janssen-Cilag GmbH, La Roche-Posay Laboratoire Dermatologique Deutschland, Novartis Pharma GmbH, Parexel International GmbH, Pfizer Deutschland GmbH, Sanofi-Aventis Deutschland GmbH, TFS Trial Form Support GmbH, UCB Pharma GmbH. G.B.E.J. is the vice president and a founding member of the EHSF, a board member of the Nordic Association of Dermatology and an honorary member of the British Association of Dermatologists. G.B.E.J. is also a member of the European Academy of Dermatology and Venereology, the American Academy of Dermatology, the Serbian Association of Dermatovenereologists, the Hungarian Society of Dermatology, the Baltic Association of Dermatovenerologists, the Finnish Society of Dermatology and the Latvian Society of Dermatology and Venereology. G.B.E.J. is the Editor-in-chief of Dermatology, commissioning editor of Clinical Problems in Dermatology, associate editor of Clinical Dermatology and Acta Dermatovenerologica Adriatica, Pannonica et Alpina, and an editorial board member of Acta Dermatovenerologica Croatica and Frontiers in Medicine. G.B.E.J. has received research grants and grants for participation as an investigator from Abbvie, Astra-Zeneca, Inflarx, Janssen-Cilag, Leo Pharma, Novartis, Regeneron and Sanofi. He has also received unrestricted departmental grants from Abbvie, Leo Pharma, and Novartis. G.B.E.J. has received honoraria from AbbVie, Chemocentryx, Coloplast, Incyte, Inflarx, Novartis, Pierre Fabre and UCB for participation on advisory boards, and has received speaker honoraria from AbbVie, Boehringer-Ingelheim, Galderma, MSD and Novartis. Ł.M. is a founding member of the EHSF and a member of the European Academy of Dermatology and Venereology and Polish Dermatological Society. Ł.M. has received research grants, travel grants, consulting honoraria or lecturer’s honoraria from AbbVie, Amgen, Behringer Ingelheim, InfraRX, Janssen, Leo Pharma, Medac, Menlo Therapeutics, Pfizer, Pierre Fabre, Polpharma, Regeneron, Novartis, Trevi, UCB and Valeant. A.B.K. is a consultant and investigator for Novartis, Abbvie, UCB, Pfizer, Lilly and Janssen. A.B.K. has received fellowship funding from Janssen and Abbvie. K.W. has received research grants, travel grants, consulting honoraria or lecturer’s honoraria from AbbVie, Bayer Schering Pharma, Biogen IDEC, Celgene, Dr. Willmar Schwabe GmbH & Co. KG, Flexopharm, Generon Corporation, Janssen-Cilag, Johnson & Johnson, Novartis, Pfizer, Sanofi-Aventis, TFS Trial Form Support and UCB. E.P. declares no competing interests.

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Glossary

Nodules

Firm swellings of the skin, mainly arising from the dermis and subcutis.

Abscesses

Red, tender, pus-containing cavities in the skin or any organ, surrounded by inflammation.

Sinus tracts

Linear, palpable, subcutaneous tunnels draining to the skin surface via an opening.

Fistulas

Permanent, abnormal tunnels between two hollow organs or from a hollow organ to the skin surface.

Plugging

The occlusion of a hair follicle or sweat gland pore by a keratin mass.

Open comedones

Wide skin pores, plugged with a mass of black keratin debris.

Double-ended pseudocomedones

Two interconnected dilated pores with a plug of black keratin debris at each end.

Pilonidal sinus

A recurrent nodule or abscess draining via a sinus in the cleft between the buttocks near the tailbone.

Furuncle

An abscess or nodule arising from a hair follicle, caused by infection with Staphylococcus aureus.

Pyoderma gangrenosum

Rare skin disease characterized by growing painful ulcers with undermined borders.

Acne conglobata

A rare and severe form of acne presenting with interconnected nodules, abscesses and sometimes sinus tracts, mostly in the neck, back and chest.

Dissecting cellulitis of the scalp

A rare condition of the scalp associated with hidradenitis suppurativa, with pus-filled or indurated lumps, scarring and permanent hair loss.

Pyogenic arthritis

Arthritis caused by invasion of a joint by an infectious agent resulting in painful joint inflammation.

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Sabat, R., Jemec, G.B.E., Matusiak, Ł. et al. Hidradenitis suppurativa. Nat Rev Dis Primers 6, 18 (2020). https://doi.org/10.1038/s41572-020-0149-1

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