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多发性表皮下钙化结节酷似发疹性黄瘤:1例报告并文献复习

Multiple sub-epidermal calcified nodule mimicking eruptive xanthoma: a case report and review of the literature.

作者信息

Ozuguz Pinar, Balta Ilknur, Bozkurt Ozlem, Unverdi Hatice, Dostbil Ahmet

机构信息

Clinic of Dermatology, Ankara Etlik Training and Research Hospital, Ankara, Turkey.

出版信息

Indian J Dermatol. 2013 Sep;58(5):406. doi: 10.4103/0019-5154.117327.

Abstract

Sub-epidermal calcified nodule (SCN) is an uncommon form of idiopathic calcinosis. It usually occurs in children, particularly in the head and neck region, presenting as a solitary, painless, yellow-white nodule with papillomatous features. These lesions occur twice as common in males compared with females. The pathogenesis is uncertain, but the clinical and histological features of this lesion are distinctive. We report a case of 22-year-old man with multiple nodules bilaterally located on the dorsum of hands simulating eruptive xanthoma. Histopathological examination of one of the excised lesion confirmed the diagnosis showing epidermal and sub-epidermal deposition of calcium. This paper presents a review of the literature and adds a new case of SCN.

摘要

表皮下钙化结节(SCN)是特发性钙质沉着症的一种罕见形式。它通常发生于儿童,尤其是头颈部区域,表现为单个、无痛、具有乳头状特征的黄白色结节。这些病变在男性中的发生率是女性的两倍。其发病机制尚不确定,但该病变的临床和组织学特征具有独特性。我们报告一例22岁男性患者,双侧手背出现多个结节,类似疹性黄瘤。对其中一个切除病变进行组织病理学检查,证实诊断为表皮和表皮下钙沉积。本文对相关文献进行了综述,并新增了一例SCN病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e30f/3778796/4cb53f8f33d4/IJD-58-406d-g002.jpg

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