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一名青春期女性上肢发生色素性痒疹的罕见病例:一种罕见的表现。

Unusual case of prurigo pigmentosa on the upper extremities in an adolescent female: A rare presentation.

作者信息

Kurmuş Gökçe Işıl, Elkıran Laden, Menteşoğlu Dilek, Ayva Ebru Şebnem, Kartal Selda Pelin

机构信息

Department of Dermatology & Venereology, Ankara Etlik City Hospital, Ankara, Turkey.

Department of Pathology, Ankara Etlik City Hospital, Ankara, Turkey.

出版信息

Pediatr Dermatol. 2025 Jan-Feb;42(1):203-205. doi: 10.1111/pde.15731. Epub 2024 Sep 3.

Abstract

A 16-year-old girl developed prurigo pigmentosa (PP) following initiation of a ketogenic diet, presenting with pruritic, erythematous, and brownish papules exclusively on her upper extremities. Histopathological examination revealed mild spongiosis with perivascular neutrophilic and mononuclear cell infiltrate, confirming the diagnosis of PP. Treatment with oral doxycycline and discontinuation of the ketogenic diet led to lesion resolution within one month, with subsequent postinflammatory hyperpigmentation. This case highlights the rarity of PP presenting solely on the upper extremities in pediatric patients, expanding our understanding of this dermatological disease.

摘要

一名16岁女孩在开始生酮饮食后患上了色素性痒疹(PP),仅在上肢出现瘙痒性、红斑性和褐色丘疹。组织病理学检查显示轻度海绵形成伴血管周围中性粒细胞和单核细胞浸润,确诊为PP。口服多西环素治疗并停用生酮饮食后,皮损在1个月内消退,随后出现炎症后色素沉着。该病例突出了小儿患者仅在上肢出现PP的罕见性,拓展了我们对这种皮肤病的认识。

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