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生物治疗能诱发皮肤局限性粘蛋白病吗?

Can biologic treatment induce cutaneous focal mucinosis?

作者信息

Lesiak Aleksandra, Włodarczyk Marcin, Sobolewska Aleksandra, Sieniawska Joanna, Rogowski-Tylman Michał, Sysa-Jedrzejowska Anna, Olejniczak-Staruch Irmina, Narbutt Joanna

机构信息

Department of Dermatology, Medical University of Lodz, Lodz, Poland. Head of the Department: Prof. Anna Sysa-Jedrzejowska MD, PhD.

出版信息

Postepy Dermatol Alergol. 2014 Dec;31(6):413-6. doi: 10.5114/pdia.2014.40944. Epub 2014 Dec 22.

Abstract

Skin mucinosis is a rare skin disease which clinically manifests as firm papules and waxy nodules. We report a case of a 66-year-old female psoriatic patient who developed skin mucinosis during biological therapy. Because of a previous lack of response to the local and conventional systemic treatment of psoriasis, the patient received biological therapy (infliximab from June 2008 to May 2009 - initial clinical improvement and loss of treatment effectiveness in the 36(th) week of the therapy; adalimumab from June 2009 to January 2010 - lack effectiveness; ustekinumab from March 2012 to the present). Throughout 2 months we observed a manifestation of the skin mucinosis as well-demarcated, yellow and brown, papulo-nodular lesions of 5-10 mm in diameter, localized on the back. Histopathological examination with alcian blue staining demonstrated mucin deposits in the dermis. On the basis of clinical and histopathological findings, the diagnosis of cutaneous focal mucinosis was established. We present the case because of the extremely rare occurrence of the disease. Scarce literature and data suggest that there is an association between focal mucinosis and thyroid dysfunction, as well as possible adverse effects of biological therapy with TNF-α antagonists.

摘要

皮肤黏蛋白沉积症是一种罕见的皮肤病,临床上表现为坚实的丘疹和蜡样结节。我们报告一例66岁的女性银屑病患者,在生物治疗期间发生了皮肤黏蛋白沉积症。由于该患者先前对银屑病的局部和传统全身治疗均无反应,因此接受了生物治疗(2008年6月至2009年5月使用英夫利昔单抗——治疗初期临床症状改善,但在治疗第36周时治疗效果丧失;2009年6月至2010年1月使用阿达木单抗——无效;2012年3月至今使用优特克单抗)。在两个月的时间里,我们观察到皮肤黏蛋白沉积症表现为边界清晰、直径5至10毫米的黄色和棕色丘疹结节性损害,位于背部。阿尔辛蓝染色的组织病理学检查显示真皮中有黏蛋白沉积。根据临床和组织病理学 findings,确诊为皮肤局灶性黏蛋白沉积症。我们展示该病例是因为这种疾病极其罕见。稀少的文献和数据表明,局灶性黏蛋白沉积症与甲状腺功能障碍之间存在关联,以及使用TNF-α拮抗剂进行生物治疗可能产生的不良反应。 (注:原文中“findings”未翻译完整,可能是笔误,推测应该是“发现”之类意思,这里直接保留英文。)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84a7/4293384/71e672456cf3/PDIA-31-22350-g001.jpg

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