A Case of Eosinophilic Granulomatosis With Polyangiitis (EGPA) Peripheral Neuropathy With Positive Anti-Myelin Oligodendrocyte (MOG) Antibodies

被引：0

作者：

Yousuf, Kauser ^{[1
]}

Ibrahim, Hadiza ^{[1
]}

Elbashari, Mahfoud ^{[2
]}

Abouelnaga, Mohamed E. ^{[2
]}

Alzaabi, Amani ^{[2
]}

机构：

[1] Zayed Mil Hosp, Internal Med, Abu Dhabi, U Arab Emirates

[2] Zayed Mil Hosp, Neurol Internal Med, Abu Dhabi, U Arab Emirates

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2023年 / 15卷 / 10期

关键词：

systemic autoimmune diseases; antineutrophil cytoplasmic antibody (anca) associated vasculitis (aav); anti-mog antibody; peripheral neuropathy; eosinophilic granulomatosis with polyangiitis (egpa); AMERICAN-COLLEGE; VASCULITIS;

D O I：

10.7759/cureus.48055

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Peripheral neuropathy is a common manifestation of Eosinophilic Granulomatosis with Polyangiitis (EGPA), a rare autoimmune disorder caused by eosinophilic infiltration of multiple organs including the nervous system. Recent research has shown an association between myelin oligodendrocyte glycoprotein (MOG) antibodies and various neurologic conditions. We present a unique case of EGPA with positive MOG antibodies in the cerebrospinal fluid (CSF) in a patient presenting with peripheral neuropathy. We also highlight a few diagnostic dilemmas with EGPA and the importance of early diagnosis and appropriate treatment. Clinical, laboratory, radiological, and electrophysiologic findings are discussed.

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页数：13

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