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一个位于不寻常部位的混合性皮肤囊肿:病例报告

A Hybrid Skin Cyst at an Unusual Location: A Case Report.

作者信息

Koleva Maria, Lisner Tomo, Mollova Angelina, Petrov Petar-Preslav, Dikov Dorian

机构信息

Department of General and Clinical Pathology, Medical University of Plovdiv, Plovdiv, BGR.

Department of Pathology, Jossigny Hospital, Jossigny, FRA.

出版信息

Cureus. 2024 Sep 1;16(9):e68378. doi: 10.7759/cureus.68378. eCollection 2024 Sep.

Abstract

Hybrid cysts originate from more than two components of the pilosebaceous unit. The pathogenesis of this cystic lesion remains unclear. Most of the investigated cases have scalp and face predilection. The lesion is predominantly observed in females. We present a case of a 69-year-old woman with a painless cutaneous nodule measuring 0.7 cm on the right calf. After a surgical excision, the histological investigation showed that the normal epidermis was elevated by a deeply encapsulated intradermal cyst, which was lined by two distinct histological types of epithelium with an abrupt transition between them. One-half of the cystic surface consisted of a keratinizing squamous layer with a granular layer and keratin lamellae, while the other half was lined by epithelium showing pilomatricial differentiation. Finally, an extremely rare diagnosis was set of a hybrid cyst.

摘要

混合性囊肿起源于毛囊皮脂腺单位的两个以上成分。这种囊性病变的发病机制尚不清楚。大多数研究病例好发于头皮和面部。该病变主要见于女性。我们报告一例69岁女性患者,右小腿有一个0.7厘米的无痛性皮肤结节。手术切除后,组织学检查显示正常表皮被一个深部包被的皮内囊肿抬高,囊肿内衬有两种不同组织学类型的上皮,两者之间有突然转变。囊肿表面的一半由有颗粒层和角蛋白薄片的角化鳞状层组成,而另一半则由显示毛母质分化的上皮衬里。最后,诊断为极为罕见的混合性囊肿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac6/11444840/fc53fe27b1ac/cureus-0016-00000068378-i01.jpg

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