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骨化性毛母质瘤及其发病机制的新假说:一例报告及全面文献复习。

Ossifying pilomatricoma and a novel hypothesis for its pathogenesis: A case report and comprehensive literature review.

机构信息

Department of Plastic and Reconstructive Surgery, Kangwon National University School of Medicine, Chuncheon, Republic of Korea.

Department of Anatomic Pathology, Kangwon National University School of Medicine, Chuncheon, Republic of Korea.

出版信息

Medicine (Baltimore). 2022 Feb 11;101(6):e28753. doi: 10.1097/MD.0000000000028753.

Abstract

RATIONALE

Pilomatricoma is a benign skin appendageal tumor derived from hair follicle matrix cells that commonly affects the head, neck, and upper extremities of the pediatric population. Since the original tumor description, diverse variants have been reported in the literature. Pilomatricoma with florid osseous metaplasia is described as an ossifying pilomatricoma and is recognized as a distinct variant of this benign tumor. However, the pathogenesis of this variant remains unclear. In this study, we present an uncommon case of ossifying pilomatricoma and address the pathogenesis of metaplastic ossification through a comprehensive literature review.

PATIENT CONCERNS

A 14-year-old boy presented with an asymptomatic protuberant mass in the preauricular region.

DIAGNOSIS

Based on its clinicopathological features, we diagnosed the lesion as an ossifying pilomatricoma.

INTERVENTIONS AND OUTCOMES

The lesion was surgically removed under local anesthesia. The postoperative course was uneventful during the 6-month postoperative follow-up.

LESSONS

We suggest that metaplastic ossification in ossifying pilomatricoma represents another feature of foreign body reaction to keratinous materials containing shadow cells in old lesions and a walling-off phenomenon to prevent exposure of surrounding tissues to keratinous materials.

摘要

理由

毛母质瘤是一种良性皮肤附属器肿瘤,来源于毛囊基质细胞,常见于儿童的头、颈和上肢。自最初的肿瘤描述以来,文献中已有多种变体报道。伴有明显骨化生的毛母质瘤被描述为骨化毛母质瘤,被认为是这种良性肿瘤的一个独特变体。然而,这种变体的发病机制尚不清楚。在本研究中,我们报告了一例不常见的骨化毛母质瘤,并通过全面的文献复习探讨了化生性骨化的发病机制。

患者关注

一名 14 岁男孩出现耳前区无症状的隆起性肿块。

诊断

根据其临床病理特征,我们诊断病变为骨化毛母质瘤。

干预和结果

病变在局部麻醉下手术切除。术后 6 个月随访期间,无任何并发症。

教训

我们认为,骨化毛母质瘤中的化生性骨化代表了对含影子细胞的角化物质的异物反应的另一个特征,这种角化物质在陈旧病变中,以及一种隔离现象,以防止周围组织暴露于角化物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ac/8830851/077f09a3fb9f/medi-101-e28753-g001.jpg

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