Subspecialty Clinics: Hematology
Lymphadenopathy

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Lymphadenopathy can occur in any age group, in symptomatic or asymptomatic patients, and in a single site or at multiple sites. Lymphadenopathy is associated with numerous disorders. An abnormal lymph node may be observed or palpated by the patient, found by a health care worker, or discovered through radiologic evaluation. Lymphadenopathy may be a part of a complex case presentation, or the clinical cause may be straightforward. Patients with potentially curable malignant disorders may have lymphadenopathy as the first sign of their disease. This review of lymphadenopathy summarizes general considerations, discusses which patients might be considered for biopsy, reviews which nodes are most likely to be diagnostic, outlines initial diagnostic considerations on a region by-region basis, and reviews a broad differential diagnosis for adenopathy.

Section snippets

Patient Age, Node Size, And Node Location

Age is the most important factor in predicting the probability of whether the lymphadenopathy is due to a benign or malignant lesion.1 Lee et al1 analyzed findings from 925 patients who underwent a lymph node biopsy at Los Angeles County Hospital between 1973 and 1977 (Table 2). This total represented 0.9% of all surgical cases at the institution during that period. Lymphoproliferative disorders were not found to have an age predilection, while carcinomas, predictably, were much more common in

Differential Diagnosis

The differential diagnosis of lymphadenopathy of unknown origin is similar to that of fever of unknown origin or an elevated erythrocyte sedimentation rate, in that most cases are due to an infection, a malignancy, or an immune disorder.33 There are 3 broad models to categorize lymphadenopathy. The extensive differential diagnosis may be grouped incorporating an acronym, CHICAGO (cancers, hypersensitivity syndromes, infections, connective tissue diseases, atypical lymphoproliferative disorders,

Special Clinical And Laboratory Associations

Historical and laboratory associations may aid in establishing the diagnosis in difficult cases associated with lymphadenopathy (Table 6). The differential diagnosis of lymphadenopathy with malabsorption includes gluten-sensitive enteropathy, Crohn disease, amyloidosis, and Whipple disease. Rheumatoid arthritis, systemic lupus erythematosus, Wegener granulomatosis, or Whipple disease may cause lymphadenopathy associated with arthralgias or arthritis. Renal disease and lymphadenopathy are seen

Conclusion

Lymphadenopathy is an important physical finding with an extensive differential diagnosis that often presents interesting challenges to the clinician. Skill in palpating peripheral lymph nodes improves with time. Clinicians should be encouraged to consistently measure the peripheral nodes that are discovered on physical examination with calipers. Node biopsies, when appropriate, should be performed in a manner most likely to yield a useful result. Knowledge of the broad differential diagnosis

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