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特应性皮炎皮损中穿凿性毛囊角化病。

Perforating lichen nitidus in the setting of atopic dermatitis.

机构信息

Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas, USA.

Department of Dermatology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Cutan Pathol. 2024 Feb;51(2):108-113. doi: 10.1111/cup.14545. Epub 2023 Oct 12.

Abstract

Perforating lichen nitidus is a rare subtype of lichen nitidus, with approximately 11 cases reported worldwide. Lesions typically present in young male patients at sites prone to mechanical irritation, including the hands, feet, forearms, elbows, and knees. Classic histopathologic features of perforating lichen nitidus show a lymphohistiocytic infiltrate within the papillary dermis between hyperplastic rete ridges with transepidermal elimination of dermal contents. Very few cases are reported in the literature of lichen nitidus and its association with atopic dermatitis. This is the first case describing perforating lichen nitidus in a patient with a history of atopic dermatitis being treated with dupilumab injections. Lesions of perforating lichen nitidus worsened with successful treatment of atopic dermatitis. These findings suggest a unique pathophysiology of perforating lichen nitidus lesions.

摘要

穿凿性毛囊角化病是毛囊角化病的一种罕见亚型,全世界约有 11 例报道。病变通常发生在易受机械刺激的年轻男性患者,包括手、脚、前臂、肘部和膝盖。穿凿性毛囊角化病的典型组织病理学特征显示,在增生的真皮网嵴之间的乳头真皮内有淋巴组织细胞浸润,表皮内有真皮内容物的排出。文献中很少有毛囊角化病及其与特应性皮炎相关的病例报道。这是首例描述特应性皮炎病史患者的穿凿性毛囊角化病病例,该患者接受了度普利尤单抗注射治疗。穿凿性毛囊角化病的皮损在特应性皮炎成功治疗后恶化。这些发现提示穿凿性毛囊角化病皮损具有独特的病理生理学机制。

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