کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3064785 | 1580455 | 2010 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
An atypical case of X-linked lymphoproliferative disease revealed as a late cerebral lymphoma
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
ایمنی شناسی و میکروب شناسی
ایمونولوژی
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چکیده انگلیسی
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.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Neuroimmunology - Volume 218, Issues 1–2, 25 January 2010, Pages 125–128
Journal: Journal of Neuroimmunology - Volume 218, Issues 1–2, 25 January 2010, Pages 125–128
نویسندگان
B. Hervier, S. Latour, D. Loussouarn, M. Rimbert, G De-Saint-Basile, C. Picard, M. Hamidou,