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Abstract

Many of the so-called errors in metabolism, the storage diseases, produce inclusions or vacuoles in the tissues of affected individuals. The placenta is often similarly involved, and chorionic villus biopsy (CVS) is now more often employed to make the diagnosis prenatally, as for instance when diagnosing lipofuscinosis (Rapola et al., 1990). Electron microscopy and special enzyme studies are usually helpful for the precise diagnosis of the defect involved. Thus, appropriate fixation is needed when such disease is suspected and it must also be anticipated at the time of CVS, as many of the inclusions are highly waterand lipid-solvent soluble. Because many of these diseases are the cause of fetal hydrops, the cases of nonimmune hydrops fetalis warrant special attention. An excellent ultrastructural study of 11 cases has been published by Jones et al. (1990) that details procedures and findings, and Fox (1997) has shown other material. These publications depict the findings in admirable detail and provide additional literature. Table 18.1 summarizes the current status of placental studies in various storage disorders.

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References

  • Abe, K., Matsuda, I., Arashima, S., Mitsuyama, T., Oka, Y. and Ishikawa, M.: Ultrastructural studies in fetal I-cell disease. Pediatr. Res. 10: 669–676, 1976.

    Article  PubMed  CAS  Google Scholar 

  • Applegarth, D.A., Toone, J.R., Wilson, R.D., Long, S.L. and Baldwin, V.J.: Morquio disease presenting as hydrops fetalis and enzyme analysis of chorionic villus tissue in a subsequent pregnancy. Pediatr. Pathol. 7: 593–599, 1987.

    Article  PubMed  CAS  Google Scholar 

  • Aula, P., Rapola, J., Autio, S., Raivio, K. and Karjalainen, O.: Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II). J. Pediatr. 87: 221–226, 1975.

    Article  PubMed  CAS  Google Scholar 

  • Aylsworth, A.S., Thomas, G.H., Hood, J.L., Malouf, N. and Libert, J.: A severe infantile sialidosis: clinical, biochemical, and microscopic features. J. Pediatr. 96: 662–668, 1980.

    Article  PubMed  CAS  Google Scholar 

  • Baker, H.J., Mole, J.A., Lindsey, J.R. and Creel, R.M.: Animal models of human ganglioside storage diseases. Fed. Proc. 35: 1193–1201, 1976.

    PubMed  CAS  Google Scholar 

  • Baldwin, V.J., Applegarth, D.A., Pantzar, T.R., Smyth, J. and McGillivray, B.C.: Congenital sialidosis (abstract). Lab. Invest. 52: 1P, 1985.

    Google Scholar 

  • Bendon, R.W. and Hug, G.: Morphologic characteristics of the placenta in glycogen storage disease type II (β-1,4glucosidase deficiency). Am. J. Obstet. Gynecol. 152: 1021–1026, 1985.

    PubMed  CAS  Google Scholar 

  • Benirschke, K. and Kaufmann, P.: Pathology of the Human Placenta, 3rd ed. Springer, New York, 1995.

    Google Scholar 

  • Bouvier, R. and Maire, I.: Fetal presentation of 23 cases of lysosomal storage disease. A collaborative study of the French Society of Fetal Pathology. Pediatr. Pathol. Lab. Med. 17: 675, 1997.

    Google Scholar 

  • Conradi, N.G., Uverbrandt, P., Hökegârd, K.-H., Wahlströmm, T. and Mellqvist, L.: First-trimester diagnosis of juvenile neuronal ceroid lipofuscinosis by demonstration of fingerprint inclusions in chorionic villi. Prenatal Diagn. 9: 283–287, 1989.

    Article  CAS  Google Scholar 

  • Cozzutto, C.: Case report. Foamy degeneration of placenta. Virchows Arch. Pathol. Anat. 401: 363–368, 1983.

    CAS  Google Scholar 

  • Desai, P.K., Astrin, K.H., Gordon, R.E., Thung, S., Strauss, L. and Desnick, R.J.: Cholesterol ester storage disease: prenatal diagnosis and fetal pathology. Lab. Invest. 52: 4P, 1985.

    Google Scholar 

  • Fox, H.: Pathology of the Placenta. 2nd Ed. Saunders, London, 1997.

    Google Scholar 

  • Gehler, J., Cantz, M., Stoeckenius, M. and Spranger, J.: Prenatal diagnosis of mucolipidosis II (I-cell disease). Eur. J. Pediatr. 122: 201–206, 1976.

    Article  PubMed  CAS  Google Scholar 

  • Gellis, S.S. and Feingold, M.: Picture of the month. I-cell disease (mucolipidosis II). Am. J. Dis. Child. 131: 1137–1138, 1977.

    Google Scholar 

  • Gillan, J.E., Lowden, J.A., Gaskin, K. and Cutz, E.: Congenital ascites as a presenting sign of lysosomal storage disease. J. Pediatr. 104: 225–231, 1984.

    Article  PubMed  CAS  Google Scholar 

  • Ginsburg, S.J. and Groll, M.: Hydrops fetalis due to infantile Gaucher’s disease. J. Pediatr. 82: 1046–1048, 1973.

    Article  PubMed  CAS  Google Scholar 

  • Giugliani, R., Dutra, J.C., Pereira, M.L.S., Rotta, N., Drachler, M. d.L., Ohlweiler, L., Neto, J.M. D.P., Pinheiro, C.E. and Breda, D.J.: GM1 gangliosidosis: clinical and laboratory findings in eight families. Hum. Genet. 70: 347–354, 1985.

    Article  PubMed  CAS  Google Scholar 

  • Granström, M.-L., Aula, P. and Rapola, J.: Kliinis-patologinen kokousselostus XY. Kudosvilijelyn avulla selvitetty aineenvaihduntasairaus. Duodecim 90: 421–430, 1974.

    PubMed  Google Scholar 

  • Hanai, J., Leroy, J. and O’Brien, J.S.: Ultrastructure of cultured fibroblasts in I-cell disease. Am. J. Dis. Child. 122: 34–38, 1971.

    PubMed  CAS  Google Scholar 

  • Herd, J.K., Dvorak, A.D., Wiltse, H.E., Eisen, J.D., Kress, B.C. and Miller, A.L.: Mucolipidosis type II. Multiple elevated serum and urine enzyme activities. Am. J. Dis. Child. 132: 1181–1186, 1978.

    PubMed  CAS  Google Scholar 

  • Hug, G., Bove, K.E., Soukup, S., Ryan, M., Bendon, R., Babcock, D., Warren, N.S. and Dignan, P.S.J.: Increased serum hexosaminidase in a woman pregnant with a fetus affected by mucolipidosis II (I-cell disease). N. Engl. J. Med. 311: 988–989, 1984.

    Article  PubMed  CAS  Google Scholar 

  • Hug, G., Chuck, G., Chen, Y.-T., Kay, H.H. and Bossen, E.H.: Chorionic villus ultrastructure in type II glycogen storage disease (Pompe’s disease). N. Engl. J. Med. 324: 342–343, 1991.

    Article  PubMed  CAS  Google Scholar 

  • Jauniaux, E., Vamos, E., Libert, J., Elknazen, N., Wilkin, R. and Hustin, J.: Placental electron microscopy and histochemistry in a case of sialic acid storage disorder. Placenta 8: 433–442, 1987.

    Article  PubMed  CAS  Google Scholar 

  • Jolly, R.D. and Walkley, S.U.: Lysosomal storage diseases of animals: an essay in comparative pathology. Vet. Pathol. 34: 527–548, 1997.

    Article  PubMed  CAS  Google Scholar 

  • Jones, C.J.P., Lendon, M., Chawner, L.E. and Jauniaux, E.: Ultra-structure of the human placenta in metabolic storage disease. Placenta 11: 395–411, 1990.

    Article  PubMed  CAS  Google Scholar 

  • Kleijer, W.J., Hoogeveen, A., Verheijen, F.W., Niermeijer, M.E, Galjaard, H., O’Brien, J.S. and Warner, T.G.: Prenatal diagnosis of sialidosis with combined neuraminidase and ßgalactosidase deficiency. Clin. Genet. 16: 60–61, 1979.

    Article  PubMed  CAS  Google Scholar 

  • Kohn, G., Livni, N., Ornoy, A., Sekeles, E., Beyth, Y., Legum, C., Bach, G. and Cohen, M.M.: Prenatal diagnosis of mucolipidosis IV by electron microscopy. J. Pediatr. 90:62–66, 1977. Laver, J., Fried, K., Beer, S.I., Iancu, T.C., Heyman, E., Bach, G. and Zeiger, M.: Infantile lethal neuraminidase deficiency (sialidosis). Clin. Genet. 23: 97–101, 1983.

    Google Scholar 

  • Lowden, J.A., Cutz, E., Conen, P.E., Rudd, N. and Doran, T.A.: Prenatal diagnosis of GM7-gangliosidosis. N. Engl. J. Med. 288: 225–228, 1973.

    Article  PubMed  CAS  Google Scholar 

  • Mahmood, K. and Haleem, A.: Placental morphology in siali- dosis: report of a case. Ann. Saudi Med. 9: 302–304, 1989.

    Google Scholar 

  • Maroteaux, R, Humbel, R., Strecker, G., Michalski, J.-C. and Mande, R.: Un nouveau type de sialidose avec atteinte renale: la nephrosialidose. Arch. Fr. Pédiatr. 35: 819–829, 1978.

    PubMed  CAS  Google Scholar 

  • Meizner, I., Levy, A., Carmi, R. and Robinsin, C.: Niemann-Pick disease associated with nonimmune hydrops fetalis. Am. J. Obstet. Gynecol. 163: 128–129, 1990.

    PubMed  CAS  Google Scholar 

  • Nagashima, K., Sakakibara, K., Endo, H., Konishi, Y., Nakamura, N., Suzuki, Y. and Abe, T.: I-cell disease (mucolipidosis II). Pathological and biochemical studies of an autopsy case. Acta Pathol. Jpn. 27: 251–264, 1977.

    CAS  Google Scholar 

  • Nelson, A., Peterson, I., Frampton, B. and Sly, W.S.: Mucopolysaccharidosis VII (ß-glucuronidase deficiency) presenting as non-immune hydrops fetalis. J. Pediat. 101: 574–576, 1982.

    Article  PubMed  CAS  Google Scholar 

  • O’Brien, J.F.: The lysosomal storage diseases. Mayo Clin. Proc. 57: 192–197, 1982.

    Google Scholar 

  • Popli, S., Leehey, D.J., Molnar, Z.V., Nawab, Z.M. and Ing, T.S.: Demonstration of Fabry’s disease deposits in placenta. Am. J. Obstet. Gynecol. 162: 464–465, 1990.

    PubMed  CAS  Google Scholar 

  • Powell, H.C., Benirschke, K., Favara, B.E. and Pflueger, O.H.: Foamy changes of placental cells in fetal storage disorders. Virchows Arch. A Pathol. Anat. Histol. 369: 191–196, 1976.

    CAS  Google Scholar 

  • Rapola, J. and Aula, R: Morphology of the placenta in fetal I-cell disease. Clin. Genet. 11: 107–113. 1977.

    Article  PubMed  CAS  Google Scholar 

  • Rapola, J., Autio, S., Aula, R. and Nanto, V.: Lymphocytic inclusions in I-cell disease. J. Pediatr. 85: 88–90, 1974.

    Article  PubMed  CAS  Google Scholar 

  • Rapola, J., Salonen, R., Ämmälä, R and Santavuori, R: Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi. Prenatal Diagn. 10: 553–559, 1990.

    Article  CAS  Google Scholar 

  • Rapola, J., Santavuori, R. and Heiskala, H.: Placental pathology and prenatal diagnosis of infantile type of neuronal ceroid-lipofuscinosis. Am. J. Med. Genet. Suppl. 5: 99–103, 1988.

    Article  PubMed  CAS  Google Scholar 

  • Rice, G.E., Mostoufi-Zadeh, M. and Driscoll, S.G.: Hydrops fetalis in Gaucher’s disease. Teratology 29: 53A–54A, 1984.

    Google Scholar 

  • Riches, W.G. and Smuckler, E.A.: A severe infantile mucolipidosis. Clinical, biochemical and pathological features. Arch. Pathol. Lab. Med. 107: 147–152, 1983.

    PubMed  CAS  Google Scholar 

  • Roberts, D.J., Ampola, M.G. and Lage, J.M.: Diagnosis of unsuspected fetal metabolic storage disease by routine placental examination. Pediat. Pathol. 11: 647–656, 1991.

    Article  CAS  Google Scholar 

  • Sarrut, S. and Belamich, R: Étude du placenta dans trois observations de dyslipide à révélation neonatale. Arch. Anat. Cytol. Pathol. 31: 187–189, 1983.

    PubMed  CAS  Google Scholar 

  • Schoenfeld, A., Abramovici, A., Klibanski, C. and Ovadia, J.: Placental ultrasonographic biochemical and histochemical studies in human fetuses affected with Niemann-Pick disease type A. Placenta 6: 33–44, 1985.

    Article  PubMed  CAS  Google Scholar 

  • Scully, R.E.: Cabot case no. 23–1997. N. Engl. J. Med. 337: 260–267, 1997.

    Article  Google Scholar 

  • See, G.L., Stanescu, R. and Lyon, G.: Un nouveau type de sialidose avec atteinte renale: la nephrosialidose. Arch. Fr. Pédiatr. 35: 830–844, 1978.

    Google Scholar 

  • Sekeles, E., Ornoy, A., Cohen, R. and Kohn, G.: Mucolipidosis IV: fetal and placental pathology. A report on two subsequent interruptions of pregnancy. Monogr. Hum. Genet. 10: 47–50, 1978.

    PubMed  CAS  Google Scholar 

  • Sidransky, E. and Ginns, E.I.: Clinical heterogeneity among patients with Gaucher’s disease. J.A.M.A. 269: 1154–1157, 1993.

    Article  PubMed  CAS  Google Scholar 

  • Stevenson, R.E., Lubinsky, M., Taylor, H.A., Wenger, D.A., Schroer, R.J. and Olmstead, P.M.: Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile type. Pediatrics 72: 441–449, 1983.

    PubMed  CAS  Google Scholar 

  • Terashima, Y., Tsuda, K., Isomura, S., Sugiura, Y. and Nogami, H.: I-cell disease. Report of three cases. Am. J. Dis. Child. 129: 1083–1090, 1975.

    PubMed  CAS  Google Scholar 

  • Vanier, M.T., Rousson, R.M., Mandon, G., Choiset, A., Lake, B.D. and Pentchev, P.G.: Diagnosis of Niemann-Pick disease type C on chorionic villus biopsy. Lancet 1: 1014–1015, 1989.

    Article  PubMed  CAS  Google Scholar 

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Benirschke, K., Kaufmann, P. (2000). Fetal Storage Disorders. In: Pathology of the Human Placenta. Springer, New York, NY. https://doi.org/10.1007/978-1-4757-4199-5_18

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  • DOI: https://doi.org/10.1007/978-1-4757-4199-5_18

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