Cranial nerve VI palsy as a rare initial presentation of systemic lupus erythematosus: case report and review of the literature

被引：13

作者：

Saleh, Z. ^{[1
]}

Menassa, J. ^{[1
]}

Abbas, O. ^{[2
]}

Atweh, S. ^{[1
]}

Arayssi, T. ^{[1
]}

机构：

[1] Amer Univ Beirut, Dept Internal Med, Med Ctr, Beirut, Lebanon

[2] Amer Univ Beirut, Dept Dermatol, Med Ctr, Beirut, Lebanon

来源：

LUPUS | 2010年 / 19卷 / 02期

关键词：

cranial nerve VI palsy; systemic lupus erythematosus; SENSORINEURAL HEARING-LOSS; VOCAL CORD PARALYSIS; PULMONARY-HYPERTENSION; ANTIPHOSPHOLIPID SYNDROME; NEUROPSYCHIATRIC MANIFESTATIONS; PAINFUL OPHTHALMOPLEGIA; PATIENT; ANTIBODIES; CLASSIFICATION; ASSOCIATION;

D O I：

10.1177/0961203309345722

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A 48-year-old woman presented with isolated sixth cranial nerve palsy. She subsequently developed systemic lupus erythematosus (SLE) based on clinical and laboratory parameters. Three years later, she presented again with sixth cranial nerve palsy affecting the contralateral eye. Within 2 weeks of steroid initiation, complete recovery occurred. The unusual rare presentation of SLE in the current patient, as well as the pathogenesis and treatment of cranial neuropathy in SLE are discussed. Lupus (2010) 19, 201-205.

引用

页码：201 / 205

页数：5

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