A Case of Sjogren's Syndrome Mimicking Inflammatory Myopathy

被引：0

作者：

Khosa, Shaweta ^{[1
]}

Hovsepian, Dominic A. ^{[2
]}

Khosa, Gurveer S. ^{[3
]}

Catherine, Yim ^{[4
]}

Trikamji, Bhavesh ^{[5
]}

Mishra, Shri K. ^{[6
]}

机构：

[1] Olive View Univ Calif Los Angeles, Med Ctr, Neurol, Los Angeles, CA USA

[2] Univ Calif Los Angeles, David Geffen Sch Med, Neurol, Los Angeles, CA 90095 USA

[3] Indira Gandhi Med Coll, Internal Med, Shimla, India

[4] Olive View Univ Calif Los Angeles, Radiol, Med Ctr, Sylmar, CA USA

[5] Harbor Univ Calif Los Angeles, Neurol, Med Ctr, Torrance, CA USA

[6] Univ Southern Calif, Keck Sch Med, Neurol, Los Angeles, CA 90007 USA

来源：

CUREUS | 2018年 / 10卷 / 10期

关键词：

myopathy; skeletal muscle; neuropathy; muscle biopsy; sjogren's syndrome;

D O I：

10.7759/cureus.3393

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Sjogren's syndrome (SS) is a chronic autoimmune disorder, characterized by lymphocytic infiltration of exocrine glands and causing the decreased function of lacrimal and salivary glands. We describe a case of a 34-year-old male who presented with Sjogren's syndrome presenting as myopathy and sensorimotor neuropathy. His creatinine kinase levels were elevated with positive anti-Sjogren's syndrome-related antigen A autoantibodies and anti-Sjogren's syndrome Type B autoantibodies. Electromyography showed evidence of irritable myopathy. Parotid gland biopsy demonstrated focal lymphocytic sialadenitis. The patient favorably responded to high-dose steroids. Thus, although rare, inflammatory myopathy must be considered part of the initial presentation of Sjogren's syndrome.

引用

页数：8

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