嗜酸性肉芽肿病合并多血管炎表现为急性鼻塞

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL
M. Abdulla
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引用次数: 0

摘要

一位55岁的男性,表现为高度发热、鼻塞和红斑性皮疹,持续1周。他患有高血压5年,未控制的糖尿病6年,支气管哮喘8年。根据临床、实验室和组织病理学检查结果,他被诊断为嗜酸性肉芽肿伴多血管炎(EGPA)。他接受了泼尼松龙1 mg/kg的治疗,该剂量在数月内逐渐减少。服用类固醇后,他的鼻腔阻塞立即得到缓解。后来发烧和皮疹消退了。我们报告了一名在EGPA血管期出现急性鼻阻塞的患者。鼻腔表现通常出现在哮喘的早期,早在血管炎期发作之前。组织病理学也应排除此类患者的侵袭性鼻窦真菌感染,尤其是当他们处于危险中时。了解这种罕见血管炎的罕见急性表现可以避免诊断难题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eosinophilic Granulomatosis with Polyangiitis Presenting as Acute Nasal Obstruction
A 55-year-old man presented with high-grade fever, nasal obstruction, and erythematous skin rash for 1 week. He had hypertension for 5 years, uncontrolled diabetes mellitus for 6 years, and bronchial asthma for the past 8 years. He was diagnosed to have eosinophilic granulomatosis with polyangiitis (EGPA) based on the clinical, laboratory, and histopathological findings. He was treated with prednisolone 1 mg/kg which was tapered over months. He had immediate relief for his nasal obstruction following steroids. Fever and skin rash subsided later. We present a patient with acute nasal obstruction during the vasculitic phase of EGPA. Nasal manifestations are usually seen during the early phase along with asthma long before the onset of vasculitic phase. Invasive fungal infections of the paranasal sinuses which can have similar presentations also should be ruled out by histopathology in such patients, especially when they are at risk. Awareness regarding such rare acute presentations of an uncommon vasculitis can avoid diagnostic dilemmas.
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来源期刊
Journal of Head & Neck Physicians and Surgeons
Journal of Head & Neck Physicians and Surgeons MEDICINE, GENERAL & INTERNAL-
CiteScore
0.30
自引率
0.00%
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0
审稿时长
15 weeks
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