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嗜酸性肉芽肿性多血管炎患者出现多发性单神经炎的独特病例。

Unique case of mononeuritis multiplex in a patient of Eosinophilic granulomatosis with polyangiitis.

作者信息

Shah Tattvam, Patel Param, Patel Mamta

机构信息

Department of Internal Medicine, B.J. Medical College, Ahmedabad, Gujarat, India.

Department of Pulmonary Medicine, Narendra Modi Medical College L.G. Hospital, Gujarat, India.

出版信息

J Family Med Prim Care. 2025 Jul;14(7):3013-3015. doi: 10.4103/jfmpc.jfmpc_1870_24. Epub 2025 Jul 21.

DOI:10.4103/jfmpc.jfmpc_1870_24
PMID:40814513
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12349800/
Abstract

INTRODUCTION

Eosinophilic granulomatosis with polyangiitis (formerly known as Churg Strauss syndrome) is a rare multisystem autoimmune disease. It is known to affect 1-3 adults/million population worldwide.

CASE

A 50-year-old woman presented to the emergency room with chief complaints of Cough with expectoration since last 7 days and right Lower limb pain and weakness since last 2 days followed by left upper limb pain and weakness since last 1 day. The diagnosis in this case was done based on a sural nerve biopsy done. Patient presented to us in her vasculitis phase with no evidence of eosinophilia however, previous lab reports show eosinophilia. She also has migratory pulmonary infiltration which we can notice when we compare an older CT scan to her most recent CT scan. Pulmonary infiltrates are seen frequently in EGPA. EGPA is an uncommon cause of migratory infiltrates. The patient also has mononeuritis multiplex with acute flares of disease in 2016, 2022 and 2024. Which is a common manifestation of EGPA often seen in 55-75% of patients.

DISCUSSION

This case could be an example of monteleukast induced EGPA, although it is difficult to establish an exact etiology. There have been numerous other cases of monteleukast induced EGPA, although the pathogenesis is unclear. EGPA continues to be an underdiagnosed condition with multiple cases being missed very year.

摘要

引言

嗜酸性肉芽肿性多血管炎(以前称为变应性肉芽肿性血管炎)是一种罕见的多系统自身免疫性疾病。已知全球每百万人口中有1 - 3名成年人受其影响。

病例

一名50岁女性因以下症状前往急诊室就诊:持续7天咳嗽伴咳痰,持续2天右下肢疼痛和无力,随后持续1天左上肢疼痛和无力。该病例的诊断基于腓肠神经活检。患者在血管炎阶段就诊时无嗜酸性粒细胞增多的证据,然而,既往实验室报告显示有嗜酸性粒细胞增多。她还存在游走性肺部浸润,当我们将她较旧的CT扫描与最新的CT扫描进行比较时可以发现。肺部浸润在嗜酸性肉芽肿性多血管炎中很常见。嗜酸性肉芽肿性多血管炎是游走性浸润的罕见病因。该患者还患有多发性单神经炎,在2016年、2022年和2024年有疾病急性发作。这是嗜酸性肉芽肿性多血管炎的常见表现,常在55% - 75%的患者中出现。

讨论

该病例可能是孟鲁司特诱发的嗜酸性肉芽肿性多血管炎的一个例子,尽管难以确定确切病因。已有许多其他孟鲁司特诱发嗜酸性肉芽肿性多血管炎的病例,尽管其发病机制尚不清楚。嗜酸性肉芽肿性多血管炎仍然是一种诊断不足的疾病,每年都有多个病例被漏诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/64fe69461a7d/JFMPC-14-3013-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/1d6752bb458d/JFMPC-14-3013-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/d6fa8d883d00/JFMPC-14-3013-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/64fe69461a7d/JFMPC-14-3013-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/1d6752bb458d/JFMPC-14-3013-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/d6fa8d883d00/JFMPC-14-3013-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/12349800/64fe69461a7d/JFMPC-14-3013-g003.jpg

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