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帕西尼和皮耶里尼特发性皮肤萎缩:病例报告及文献综述

Idiopathic Atrophoderma of Pasini and Pierini: A Case Report and Literature Review.

作者信息

Hubail Rawan, Karaidi Noor, Al Awadhi Ameen

机构信息

Dermatology, Salmaniya Medical Complex, Manama, BHR.

出版信息

Cureus. 2022 Jul 5;14(7):e26571. doi: 10.7759/cureus.26571. eCollection 2022 Jul.

Abstract

Atrophoderma of Pasini and Pierini (APP) is a rare cutaneous condition of unknown etiology, predominantly affecting young women. It is a dermatologic disorder characterized by hyperpigmented depressed patches of dermal atrophy. Patients usually present with single or multiple asymptomatic, violaceous, and sharply demarcated areas of depressed plaques; of note, unlike morphea, there is no surrounding erythema or induration. In this report, we discuss a case of a 43-year-old South Asian male patient who presented with an eight-month history of multiple asymptomatic, and depressed bluish-brown plaques that had appeared over his body. The clinicopathological correlation was consistent with a diagnosis of idiopathic atrophoderma of Pasini and Pierini (IAPP). We also engage in a review of the literature on IAPP.

摘要

帕西尼和皮耶里尼皮肤萎缩症(APP)是一种病因不明的罕见皮肤病,主要影响年轻女性。它是一种以真皮萎缩性色素沉着斑为特征的皮肤病。患者通常表现为单个或多个无症状、紫罗兰色且边界清晰的凹陷斑块;值得注意的是,与硬斑病不同,周围没有红斑或硬结。在本报告中,我们讨论了一例43岁的南亚男性患者,他有8个月的病史,身上出现了多个无症状的凹陷蓝棕色斑块。临床病理相关性与特发性帕西尼和皮耶里尼皮肤萎缩症(IAPP)的诊断一致。我们还对IAPP的文献进行了综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/376c/9351397/b32951cbf46f/cureus-0014-00000026571-i01.jpg

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