单侧前干受累的急性全身性红斑性脓疱病的不寻常表现。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Medical Bulletin of Sisli Etfal Hospital Pub Date : 2024-12-24 eCollection Date: 2024-01-01 DOI:10.14744/SEMB.2024.57431
Ilknur Kivanc Altunay, Cemre Akpulat Tekin, Ilayda Esna Gulsunay, Ahmet Kayaalti, Ceylan Bulat, Seyhan Ozakkoyunlu Hascicek
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引用次数: 0

摘要

急性全身性脓疱病(AGEP)是一种罕见的药疹,其特征是许多无菌,非滤泡性脓疱,中性粒细胞增多,高热,通常在两周内自行消退。皮疹多发于躯干及三节间区。在治疗中,必须先停用致病性药物。根据患者的症状和AGEP严重程度,通常使用局部皮质类固醇、保湿剂、退烧药和全身皮质类固醇。环孢素和静脉注射免疫球蛋白治疗可用于一些严重AGEP中对全身皮质类固醇耐药的AGEP患者。我们在此报告一个独特的AGEP病例,该病例具有不同的皮疹分布和对全身皮质类固醇的抵抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unusual Presentation of Acute Generalized Exanthematous Pustulosis with Unilateral Anterior Trunk Involvement.

Acute generalized exanthematous pustulosis (AGEP) is a rare drug eruption characterized by the rapid occurrence of many sterile, non-follicular pustules, neutrophilic leukocytosis, high fever and spontaneous resolution usually within two weeks. The distribution of rash predilection in the trunk and intertriginous regions. In treatment, the causative drug must be initially discontinued. Topical corticosteroids, moisturizers, antipyretics, and systemic corticosteroids are generally used according to the patient's symptoms and AGEP severity. Cyclosporine and intravenous immunoglobulin therapy can be used in some patients with AGEP resistant to systemic corticosteroids in severe AGEP. We herein aim to report a unique case of AGEP that has different rash distribution and resistance to systemic corticosteroids.

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来源期刊
Medical Bulletin of Sisli Etfal Hospital
Medical Bulletin of Sisli Etfal Hospital MEDICINE, GENERAL & INTERNAL-
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