两种罕见病1例:毛霉病和肉芽肿性多血管炎1例。

IF 1 Q4 INFECTIOUS DISEASES Case Reports in Infectious Diseases Pub Date : 2023-01-01 DOI:10.1155/2023/7934700
Syeda Aasia Batool, Usha Kumari, Salim Surani
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摘要

毛霉菌病是一种罕见但致命的疾病,由丝状真菌引起,涉及鼻子,鼻窦和大脑。这些微生物通常在免疫功能低下的个体中引起严重感染。肉芽肿性多血管炎(GPA),又称Wegner肉芽肿病,是一种罕见的无菌性坏死性肉芽肿性血管炎,累及中小型血管,常累及鼻、耳、肺和肾脏。在同一患者中同时发生毛霉病和GPA这两种罕见疾病是极为罕见的。在这个病例研究中,我们描述了一位40岁的女性,她同时表现为GPA和毛霉菌病。她开始使用类固醇和抗真菌药物,并取得了显着改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis.

Mucormycosis is a rare but fatal disease caused by a filamentous fungus involving the nose, paranasal sinuses, and brain. These organisms usually cause severe infections in immunocompromised individuals. Granulomatous polyangiitis (GPA), also known as Wegner's granulomatosis, is a rare, aseptic necrotizing granulomatous vasculitis involving small and medium-sized vessels commonly affecting the nose, ears, lungs, and kidneys. The simultaneous occurrence of mucormycosis and GPA, two rare diseases, in the same patient is exceedingly rare. In this case study, we describe a 40-year-old woman who presented with manifestations of both GPA and mucormycosis. She was started with steroids and antifungal agents and achieved significant improvement.

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审稿时长
13 weeks
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