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眼附属器毛发基质瘤:3 例具有不同组织病理学表现的病例报告。

Pilomatrixoma of the ocular adnexa: report of 3 cases with variations in the histopathological findings.

机构信息

Departments of Ophthalmology, The Ottawa Hospital and University of Ottawa, Ottawa, Ont.; Departments of Pathology and Laboratory Medicine, The Ottawa Hospital and University of Ottawa, Ottawa, Ont.

Departments of Ophthalmology, The Ottawa Hospital and University of Ottawa, Ottawa, Ont.; Departments of Pathology and Laboratory Medicine, The Ottawa Hospital and University of Ottawa, Ottawa, Ont..

出版信息

Can J Ophthalmol. 2019 Aug;54(4):413-416. doi: 10.1016/j.jcjo.2018.10.015. Epub 2019 Jan 16.

Abstract

OBJECTIVE

To report the clinical and variations in the histopathological features of pilomatrixoma of the ocular adnexa in 3 young individuals.

DESIGN

A retrospective case series was performed with clinical, histological, and immunohistochemical analysis.

PARTICIPANTS

Case 1 is an 18-year-old male who presented with a reddish-blue swelling under the left eyebrow. The lesion measured 2 × 1 cm. Case 2 is a 2-year-old female who presented with a reddish-blue nodule inferior to the right eyebrow with telangiectatic vessels. The lesion measured 6 × 4 × 4 mm. Case 3 is a 14-year-old female who presented with a subcutaneous lesion under the right upper eyebrow with fluctuating inflammation. The lesion measured 12 × 3 × 2 mm. Histopathological examination of case 1 disclosed peripheral basaloid cells and central shadow cells containing calcific foci, separated by a transition zone. In case 2, histopathological analysis revealed central calcific foci in islands of shadow cells with more peripheral basaloid cells. In case 3, we observed numerous clusters of shadow cells with focal calcifications, as well as basaloid cells in a disorganized configuration.

CONCLUSION

Pilomatrixoma is an uncommon benign skin neoplasm originating from the matrix of the hair root. We describe a spectrum of histopathological findings in pilomatrixoma of the ocular adnexal in 3 young individuals.

摘要

目的

报告 3 例发生于眼部附属器的毛发基质瘤的临床和组织病理学特征的变异情况。

设计

对 3 例患者进行了回顾性病例系列研究,对其进行了临床、组织学和免疫组织化学分析。

参与者

病例 1 为 18 岁男性,左眼眉下有蓝色红斑性肿胀。病变大小为 2×1cm。病例 2 为 2 岁女性,右眉下有蓝色结节,伴毛细血管扩张。病变大小为 6×4×4mm。病例 3 为 14 岁女性,右上眉下有一皮下病变,伴有波动性炎症。病变大小为 12×3×2mm。病例 1 的组织病理学检查显示,周边为基底样细胞,中央为影细胞,含有钙化灶,两者之间有过渡区。病例 2 的组织病理学分析显示,中央为影细胞岛状的钙化灶,周边为基底样细胞。病例 3 观察到大量影细胞簇伴局灶性钙化,以及排列紊乱的基底样细胞。

结论

毛发基质瘤是一种起源于毛囊基质的罕见良性皮肤肿瘤。我们描述了 3 例发生于眼部附属器的毛发基质瘤的一系列组织病理学表现。

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