一例部分免疫球蛋白a缺乏患者首次出现坏疽性脓皮病

Ş. Demirel, M. Shetty, M. Patel, K. Mahmood
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引用次数: 0

摘要

我们描述了一个58岁的女性的情况下,强烈的疼痛和迅速扩大坏死性皮肤溃疡的背景下,部分免疫球蛋白a缺乏症(IgAD)的右胫骨。她被各种医疗保健专业人员看到,并使用升级抗生素治疗蜂窝织炎,需要住院治疗。皮肤科小组在评估患者出现症状13天后作出溃疡性坏疽性脓皮病(PG)的临床诊断。患者对类固醇和口服四环素有显著反应。本病例强调了PG和IgAD之间不同寻常的关联,以及PG患者的诊断挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
Summary We describe the case of a 58-year-old female with an intensely painful and rapidly enlarging necrotic cutaneous ulcer to the right shin on a background of partial immunoglobulin A deficiency (IgAD). She was seen by various healthcare professionals and managed with upscaling antibiotics for cellulitis requiring an inpatient hospital stay. The dermatology team made a clinical diagnosis of ulcerative Pyoderma Gangrenosum (PG) on assessing the patient 13 days post-onset of symptoms. The patient responded dramatically to steroids and oral tetracycline. This case highlights the unusually described association between PG and IgAD as well as the diagnostic challenge seen in patients presenting with PG.
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来源期刊
自引率
0.00%
发文量
16
审稿时长
12 weeks
期刊介绍: JRSM Open is a peer reviewed online-only journal that follows the open-access publishing model. It is a companion journal to the Journal of the Royal Society of Medicine. The journal publishes research papers, research letters, clinical and methodological reviews, and case reports. Our aim is to inform practice and policy making in clinical medicine. The journal has an international and multispecialty readership that includes primary care and public health professionals.
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