University of Florida, Gainesville, FL, USA.
J Investig Med High Impact Case Rep. 2020 Jan-Dec;8:2324709620940496. doi: 10.1177/2324709620940496.
A 59-year-old male presented with 1 month of progressive dyspnea, 30-lb weight loss, and skin changes on the digits of the hands. In the 4 weeks prior to admission, he was admitted and treated twice for pneumonia at another hospital and received intravenous (IV) vancomycin, ceftriaxone, and azithromycin for a total of 10 days. After admission, he underwent computed tomography imaging of chest, which revealed findings suggestive of interstitial lung disease but given the fact that infection was not ruled out, empiric antibiotics were initiated. The skin lesions on the fingers were felt to be consistent with Gottron's papules, and his overall constellation of findings were felt to be consistent with dermatomyositis (DM). Over the following 3 days, he developed diffuse, violaceous skin lesions, elevation of liver transaminases, and severe thrombocytopenia. The skin lesions progressed to epidermal necrosis. He developed erosions of the oral mucosa and scrotum. Before skin biopsy results were finalized, IV immunoglobulin and IV dexamethasone were started empirically for suspected DM and immune-mediated thrombocytopenia. His laboratory abnormalities normalized within a week. Biopsy results of the skin were consistent with Stevens-Johnson syndrome (SJS). Autoantibody test for anti-MDA5 were positive, confirming a diagnosis of anti-MDA5 associated DM. Subsequent development of SJS was likely due to antibiotic exposure in the preceding month. Simultaneous development of anti-MDA5 DM and SJS raises the question of a link between the 2 conditions. To our knowledge, this is the first reported association of these 2 conditions reported in the literature.
一位 59 岁男性因进行性呼吸困难、30 磅体重减轻和手部手指皮肤改变而就诊。在入院前的 4 周内,他曾因肺炎两次入住另一家医院,并接受了静脉(IV)万古霉素、头孢曲松和阿奇霉素治疗,总疗程为 10 天。入院后,他接受了胸部计算机断层扫描成像,结果显示存在间质性肺病的表现,但由于未排除感染,故开始使用经验性抗生素。手指上的皮肤病变被认为符合 Gottron 丘疹,他的整体表现被认为符合皮肌炎(DM)。在接下来的 3 天里,他出现弥漫性、紫红色皮肤病变、肝转氨酶升高和严重血小板减少。皮肤病变进展为表皮坏死。他出现口腔黏膜和阴囊糜烂。在最终确定皮肤活检结果之前,出于对疑似 DM 和免疫介导性血小板减少的考虑,开始进行 IV 免疫球蛋白和 IV 地塞米松的经验性治疗。他的实验室异常在一周内恢复正常。皮肤活检结果与史蒂文斯-约翰逊综合征(SJS)一致。抗 MDA5 自身抗体检测呈阳性,确诊为抗 MDA5 相关 DM。随后发生的 SJS 可能是由于前一个月的抗生素暴露。抗 MDA5 DM 和 SJS 的同时发生引发了这两种疾病之间是否存在关联的问题。据我们所知,这是文献中首次报道这两种疾病之间存在关联。