Myositis in infiltrative lymphocytosis syndrome: clinicopathological observations and treatment

被引：6

作者：

Attarian, S

Mallecourt, C

Donnet, A

Pouget, J

Pellisser, JF

机构：

[1] CHU Timone, Dept Neurol & Neuromuscular Dis, F-13385 Marseille, France

[2] CHU Timone, Dept Neurosurg, F-13385 Marseille, France

[3] CHU Timone, Dept Anatomopathol, F-13385 Marseille, France

来源：

NEUROMUSCULAR DISORDERS | 2004年 / 14卷 / 11期

关键词：

DILS; HIV-associated polymyositis; intranuclear inclusions;

D O I：

10.1016/j.nmd.2004.05.018

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Diffuse infiltrative lymphocytosis syndrome (DILS) is characterized by the presence of persistent circulating CDs lymphocytosis and visceral CDs lymphocytic infiltration, predominantly in the salivary glands and lungs in a subset of human immunodeficiency virus (HIV) patients. Myositis has been rarely documented in DILS. We report here the histopathological abnormalities and treatment response of an HIV patient with DILS associated myositis. Muscle biopsy revealed features of polymyositis but electron microscopy study showed intranuclear filamentous inclusions of 18 nm diameter, without intracytoplasmic inclusion. Treatment with intravenous immunoglobuline was useful. (C) 2004 Published by Elsevier B.V.

引用

页码：740 / 743

页数：4

共 13 条

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