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[Castleman病中的外周血多克隆浆细胞增多症及白细胞破碎性血管炎]

[Polyclonal plasmacytosis in peripheral blood and leukocytoclastic vasculitis in Castleman's disease].

作者信息

Izutsu K, Usuki K, Inoue K, Endo M, Iki S, Matsuya S, Urabe A

机构信息

Division of Hematology, Kanto Teishin Hopital.

出版信息

Rinsho Ketsueki. 1998 Mar;39(3):210-5.

PMID:9577645
Abstract

A 62 year-old man had fever, splenomegaly, systemic lymphadenopathy and palpable petechiae. Laboratory studies showed leukocytosis (10,200/microliters) with plasma cells (23%) and polyclonal gammopathy. Southern blot analysis of peripheral blood mononuclear cells showed no rearrangement of immunoglobulin genes, indicating polyclonal plasmacytosis in peripheral blood. A diagnosis of Castleman's disease was made by the cervical lymph node biopsy, which showed onion-skin structures in the germinal centers and plasmacytosis in the interfollicular region. A skin biopsy of the purpura lesion disclosed leukocytoclastic vasculitis. This is an unusual case of Castleman's disease presenting plasmacytosis in peripheral blood and leukocytoclastic vasculitis.

摘要

一名62岁男性出现发热、脾肿大、全身淋巴结病及可触及的瘀点。实验室检查显示白细胞增多(10,200/微升),伴有浆细胞(23%)及多克隆丙种球蛋白病。外周血单核细胞的Southern印迹分析显示免疫球蛋白基因无重排,提示外周血多克隆浆细胞增多。经颈部淋巴结活检诊断为Castleman病,活检显示生发中心有洋葱皮样结构,滤泡间区有浆细胞增多。紫癜皮损的皮肤活检显示白细胞破碎性血管炎。这是一例不寻常的Castleman病,表现为外周血浆细胞增多及白细胞破碎性血管炎。

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