Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3064785 | Journal of Neuroimmunology | 2010 | 4 Pages |
Abstract
X-linked lymphoproliferative disease (XLP) is an inherited immunodeficiency, partially characterized by a defect in cytotoxicity to Epstein-Barr virus. This viral infection is therefore often fatal in affected boys, whilst a variety of immune disorders or proliferative diseases may occur in surviving patients.We report an atypical case of a 41 year-old male who presented with a primitive B-cell cerebral lymphoma, revealing an XLP.This presentation was unusual because of its late onset, the broad spectrum of the familial characteristics, its initial presentation as a cerebral lymphoma, and the occurrence of B-cell alymphocytosis associated with a-gamma-globulinemia.
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Authors
B. Hervier, S. Latour, D. Loussouarn, M. Rimbert, G De-Saint-Basile, C. Picard, M. Hamidou,