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成人斯蒂尔病伴类色素性痒疹样皮肤疹。

Adult-onset Still's disease with prurigo pigmentosa-like skin eruption.

作者信息

Tomaru Kahori, Nagai Yayoi, Ohyama Naoko, Hasegawa Michiko, Endo Yukie, Tamura Atsushi, Ishikawa Osamu

机构信息

Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan.

出版信息

J Dermatol. 2006 Jan;33(1):55-8. doi: 10.1111/j.1346-8138.2006.00011.x.

Abstract

A 34-year-old woman with adult-onset Still's disease (AOSD) developed prurigo pigmentosa-like lesions on her chest and upper back in addition to the typical rash of AOSD. A biopsy specimen taken from the upper back showed characteristic features of prurigo pigmentosa. The eruption and fever subsided immediately after the administration of 40 mg/day prednisolone, but arthralgia persisted even after intravenous pulse methylprednisolone therapy in combination with immunosuppressive drugs. Various atypical skin rashes, including prurigo pigmentosa-like lesions, have been reported in association with AOSD. Therefore, one should carefully follow the clinical course of a patient in order not to overlook these atypical cutaneous manifestations of AOSD.

摘要

一名34岁患成人斯蒂尔病(AOSD)的女性,除了有AOSD的典型皮疹外,胸部和上背部还出现了类色素性痒疹样皮损。取自上背部的活检标本显示出色素性痒疹的特征性表现。给予40mg/天泼尼松龙后,皮疹和发热立即消退,但即使在静脉注射脉冲甲基泼尼松龙治疗联合免疫抑制药物后,关节痛仍持续存在。包括类色素性痒疹样皮损在内的各种非典型皮疹已被报道与AOSD相关。因此,为了不忽视AOSD的这些非典型皮肤表现,应仔细跟踪患者的临床病程。

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