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以双侧面瘫为表现的抗核抗体阴性系统性红斑狼疮

Antinuclear antibody negative systemic lupus erythematosus presenting as bilateral facial paralysis.

作者信息

Blaustein D A, Blaustein S A

机构信息

Department of Internal Medicine, Long Island College Hospital, State University of New York, Brooklyn 11201, USA.

出版信息

J Rheumatol. 1998 Apr;25(4):798-800.

PMID:9558189
Abstract

Cranial neuropathy, and particularly facial palsy, is a rare occurrence in patients with systemic lupus erythematosus (SLE). We describe a 16-year-old female who developed bilateral facial palsy concomitant with cutaneous bullous eruption, alopecia, mucosal ulcers, arthritis, lymphadenopathy, parotid enlargement, and proteinuria. The lack of positive antinuclear antibody (ANA) at presentation obscured the diagnosis. Her followup course clarified the diagnosis of SLE. We believe this is the first report of ANA negative SLE presenting as bilateral facial palsy.

摘要

颅神经病变,尤其是面神经麻痹,在系统性红斑狼疮(SLE)患者中较为罕见。我们描述了一名16岁女性,她出现双侧面神经麻痹,同时伴有皮肤大疱性皮疹、脱发、黏膜溃疡、关节炎、淋巴结病、腮腺肿大和蛋白尿。就诊时抗核抗体(ANA)阴性使诊断变得模糊。她的后续病程明确了SLE的诊断。我们认为这是首例以双侧面神经麻痹为表现的ANA阴性SLE报告。

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