排他性和孤立性面部毛孔扩张症:一种罕见实体的发病机制和文献再评价。

IF 0.9 Q4 DERMATOLOGY
Case Reports in Dermatology Pub Date : 2023-09-05 eCollection Date: 2023-01-01 DOI:10.1159/000530936
Giovanni Paolino, Matteo Riccardo Di Nicola, Marina Yarygina, Carlo Mattozzi, Eduardo Quaranta, Vittoria Giulia Bianchi, Michele Donati, Santo Raffaele Mercuri
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引用次数: 0

摘要

气孔再生病是一组众所周知的临床上不同的实体,其特征是不同的临床方面,但有一个共同的组织学方面,即角片层。通常,多孔性角化病发生在四肢和躯干,而很少涉及面部,尤其是作为一种独特的、单一的和孤立的病变。我们报告了一例52岁的高加索女性,她有11个月的左颧骨2厘米缓慢生长的孤立性角化病变史。患者面部和其他身体部位没有出现其他皮肤损伤。皮肤活检显示表皮增生,具有多个清晰的角状片层,与颗粒层的潜在衰减和棘层中分散的角化不良细胞有关。真皮下浅层显示轻度淋巴细胞浸润和纤维化,胶原束重塑。最后诊断为孤立性面部多孔性角化病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exclusive and Solitary Facial Porokeratosis: Pathogenesis and Literature Reappraisal of a Rare Entity.

Exclusive and Solitary Facial Porokeratosis: Pathogenesis and Literature Reappraisal of a Rare Entity.

Exclusive and Solitary Facial Porokeratosis: Pathogenesis and Literature Reappraisal of a Rare Entity.

Porokeratosis is a group of well-known clinically distinct entities, characterised by different clinical aspects, but sharing a single common histological aspect, namely the cornoid lamella. Usually, porokeratosis occurs in the limbs and trunk, while it rarely involves the face, especially as an exclusive, single, and solitary lesion. We report the case of a 52-year-old Caucasian woman, with an 11-month history of a 2-cm slowly growing solitary, keratotic lesion on her left cheekbone. The patient did not present other cutaneous lesions on the face, as well as in other body sites. A cutaneous biopsy showed epidermal hyperplasia with multiple, sharply defined cornoid lamella, associated with an underlying attenuation of the granular layer and scattered dyskeratotic cells in the spinous layer. The superficial dermis underneath showed a mild lymphocytic infiltrate and fibrosis with remodelled collagen bundles. A final diagnosis of solitary facial porokeratosis was made.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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