Metronidazole-induced linear immunoglobulin A disease in a patient suffering from ulcerative colitis: a case report and focused review of the literature

IF 2.3 Q2 DERMATOLOGY Dermatology Reports Pub Date : 2023-08-29 DOI:10.4081/dr.2023.9831
Stefano Buffon, Michele Parietti, Andrea Carugno, Elisa Robustelli Test, Angelo Valerio Marzano, Paolo Sena, Pamela Vezzoli
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Abstract

Linear immunoglobulin (Ig) A disease (LAD) is a rare autoimmune blistering dermatosis caused by linear deposition of IgA1 along the dermoepidermal junction of skin and mucosae. It can affect both children and adults. Although idiopathic in most cases, it can also be associated with infections, malignancies, or drug administration. Among medications, antibiotics are most commonly responsible, particularly vancomycin. We report the case of a 51-year-old female patient who developed mucocutaneous LAD after oral metronidazole administration, which was confirmed by histopathological examination and direct immunofluorescence of one of the bullous lesions. Lesions rapidly cleared after metronidazole discontinuation and a short course of oral methylprednisolone and dapsone. To our knowledge, this is the third reported case of metronidazole-induced LAD, and the first in which metronidazole was not administered in combination with other antibiotics such as ceftriaxone.
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甲硝唑诱导的溃疡性结肠炎患者的线性免疫球蛋白A疾病:一例报告和文献综述
线性免疫球蛋白(Ig) A病(LAD)是一种罕见的自身免疫性起泡性皮肤病,由IgA1沿皮肤和粘膜的真皮表皮连接处线性沉积引起。它可以影响儿童和成人。虽然在大多数情况下是特发性的,但它也可能与感染、恶性肿瘤或药物管理有关。在药物治疗中,抗生素是最常见的原因,尤其是万古霉素。我们报告一例51岁女性患者口服甲硝唑后发生粘膜皮肤LAD,经组织病理学检查和其中一个大疱性病变的直接免疫荧光证实。停用甲硝唑和短期口服甲基强的松龙和氨苯砜后,病变迅速清除。据我们所知,这是第三例甲硝唑诱发LAD的报告病例,也是第一例甲硝唑未与头孢曲松等其他抗生素联合使用的病例。
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来源期刊
Dermatology Reports
Dermatology Reports DERMATOLOGY-
CiteScore
1.40
自引率
0.00%
发文量
74
审稿时长
10 weeks
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