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幼年型皮肌炎伴罕见皮肤表现:广泛性多毛症。

Juvenile Dermatomyositis With Rare Cutaneous Manifestation: Generalised Hypertrichosis.

机构信息

Department of Medicine, Medical Teaching Institute, Lady Reading Hospital, Peshawar, Pakistan.

Department of Dermatology, Medical Teaching Institute, Lady Reading Hospital, Peshawar, Pakistan.

出版信息

J Pak Med Assoc. 2023 Jul;73(7):1539-1541. doi: 10.47391/JPMA.7453.

Abstract

Juvenile dermatomyositis (JDM) is a rare autoimmune disease characterised by inflammation of muscles and skin with extra muscular involvement of joints, heart, intestine, and liver. Pathogenesis of JDM is believed to be due to vasculopathy. Along with classic cutaneous features of JDM, rare findings include hypertrichosis, lipoatrophy, photosensitivity, bullous lesions, and hyperhidrosis. We present, here, a case of JDM with hypertrichosis as very few cases have been reported previously.

摘要

幼年特发性皮肌炎(JDM)是一种罕见的自身免疫性疾病,其特征为肌肉和皮肤炎症,伴有肌肉外关节、心脏、肠和肝脏受累。JDM 的发病机制被认为是由于血管病变。除了 JDM 的典型皮肤特征外,罕见的表现还包括多毛症、脂肪萎缩、光敏性、大疱性皮损和多汗症。我们在此介绍一例 JDM 伴多毛症病例,因为此前报道的病例很少。

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