Panniculitis in Anti-MDA-5 Positive Juvenile Dermatomyositis: A Case Report.

JNMA; journal of the Nepal Medical Association Pub Date : 2025-01-01 Epub Date: 2025-01-31 DOI:10.31729/jnma.8874
Semra Ayduran, Gulsah Kilbas, Saadet Nilay Tigrak, Selcuk Yuksel, Erdem Comut, Serkan Turkucar
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Abstract

Panniculitis is a rare clinical finding in dermatomyositis. There are few reported cases in the medical literature. In this report, we describe a 17-year-old male patient with anti-MDA5 positive hypomyopathic dermatomyositis who, eight months after diagnosis, presented with indurated nodules on the right forearm and right thigh despite methotrexate and monthly intravenous immunoglobulin treatment. A skin biopsy revealed lobular panniculitis with lymphocytic infiltrate. His lesions were successfully controlled with hydroxychloroquine and azathioprine. This article presents a case regarding the rarity of panniculitis in juvenile dermatomyositis and its treatment strategy.

抗mda -5阳性青少年皮肌炎并发泛膜炎1例报告。
皮肌炎是皮肌炎中一种罕见的临床表现。在医学文献中很少有病例报道。在这个报告中,我们描述了一个17岁的男性患者,患有抗mda5阳性的低肌病皮肌炎,在诊断后8个月,尽管甲氨蝶呤和每月静脉注射免疫球蛋白治疗,但在右前臂和右大腿出现硬化结节。皮肤活检显示小叶性绒毛炎伴淋巴细胞浸润。他用羟氯喹和硫唑嘌呤成功地控制了他的病变。本文报告一例关于青少年皮肌炎罕见性皮肌炎的病例及其治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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