中枢性尿囊症并发嗜酸性肉芽肿合并多血管炎1例报告并文献复习。

IF 1.1
Tatsuaki Kosaka, Shinya Yamamoto, Naoko Yasugi, Sayaka Sugioka, Takuro Hakata, Rintaro Saito, Ryosuke Hiwa, Sho Koyasu, Yuki Teramoto, Motoko Yanagita
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引用次数: 0

摘要

中枢性尿崩症(CDI)可发展为获得性全身性疾病。然而,嗜酸性肉芽肿病合并多血管炎(EGPA)并发CDI的病例是罕见的。我们在此报告一例CDI后的EGPA。一名68岁女性,有30年鼻窦炎和哮喘病史,并发CDI,随后出现严重肾功能障碍伴嗜酸性粒细胞增多和MPO-ANCA水平升高。肾活检证实EGPA。强化治疗导致透析停止,而AVP分泌的部分改善提示EGPA和CDI之间的潜在联系。我们也对并发EGPA和CDI进行了文献综述。临床医生应注意哮喘或鼻窦炎CDI患者的EGPA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Eosinophilic Granulomatosis with Polyangiitis Following Development of Central Diabetes Insipidus: A Case Report and Literature Review.

Central diabetes insipidus (CDI) can develop as an acquired systemic disease. However, cases of eosinophilic granulomatosis with polyangiitis (EGPA) with concurrent CDI are rare. We herein report a case of EGPA following CDI. A 68-year-old woman with a 30-year history of sinusitis and asthma developed CDI, followed by severe renal dysfunction with eosinophilia and elevated MPO-ANCA levels. A renal biopsy confirmed EGPA. Intensive treatment resulted in dialysis discontinuation, while partial improvement in AVP secretion suggested a potential link between EGPA and CDI. We also conducted a literature review on concurrent EGPA and CDI. Clinicians should be aware of EGPA in CDI patients with asthma or sinusitis.

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