Prolonged Vancomycin-Induced Linear IgA Disease in a Patient With Renal Failure

Kaori Takezawa, Reiko Noborio, Yuki Nomura, Takahiro Kiyohara, Mako Mine, Takashi Hashimoto
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Abstract

A 64-year-old man with pneumococcal septic shock and subsequent renal failure underwent treatments with antibiotics including intravenous vancomycin (VCM). Blistering skin lesions appeared 10 days after the initiation of VCM. When the patient was transferred to us 5 months later, blisters with erythema were still observed on the abdomen and thighs. Histopathological examination revealed subepidermal blister with infiltration of eosinophils and neutrophils, and direct immunofluorescence revealed linear IgA deposition at the basement membrane zone. The diagnosis of linear IgA disease (LAD)was made, and drug-induced LAD by VCM was suspected, because of the episode of the blister development 10 days after the first VCM administration. Although the results of various sero-immunological tests were negative, IgA reactivity with type Ⅶ collagen was detected by VCM-treated ELISA, which further suggested the diagnosis of VCM-induced LAD. The possible mechanism for the prolonged disease course was speculated.

肾功能衰竭患者万古霉素引起的线状IgA疾病的延长
一名64岁男子因肺炎球菌感染性休克和随后的肾功能衰竭接受抗生素治疗,包括静脉注射万古霉素(VCM)。VCM开始后10天出现皮肤水泡。5个月后,患者转至我们处,腹部和大腿仍可见水疱伴红斑。组织病理学检查示表皮下水泡伴嗜酸性粒细胞和中性粒细胞浸润,直接免疫荧光示基底膜区线性IgA沉积。诊断为线状IgA病(LAD),怀疑是VCM引起的药物性LAD,因为第一次给药后10天出现水疱。虽然各项血清免疫检测结果均为阴性,但经vcm处理的ELISA检测IgA与Ⅶ型胶原的反应性,进一步提示vcm诱导的LAD的诊断。对病程延长的可能机制进行了推测。
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