眼睑毛基质瘤19例临床病理特征分析。

Pub Date : 2022-02-01 DOI:10.1159/000520219
Sepideh Siadati, Ashley A Campbell, Timothy McCulley, Charles G Eberhart
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引用次数: 1

摘要

毛根基质瘤是一种相对罕见的良性肿瘤,起源于发根基质。它经常发生在头部和颈部,大多数累及眼周区域的眉毛。相反,眼睑毛基质瘤较少见,临床上常误诊。在此,我们报告19例眼睑毛基质瘤的临床和组织学资料。方法:本研究是自1981年以来本院诊断的眼睑毛基质瘤的回顾性研究。所有的幻灯片都被审查,并获得了人口统计学和临床数据。结果:患者年龄2 ~ 63岁(平均24岁),其中女性12例(63%),男性7例(37%)。8例(42%)和4例(21%)分别发生在生命的第一个和第二个十年。14例(74%)患者上眼睑受累。镜下肿瘤表现为基底样细胞、阴影细胞伴钙化及异物巨细胞。结论:眼睑毛瘤在临床上很少被怀疑,容易与囊肿、皮脂腺癌、皮脂腺癌等肿瘤相混淆。医生应考虑眼睑区域毛基质瘤的可能性,特别是儿童或年轻女性患者。完全切除是可以治愈的,诊断通常可以通过组织病理学检查来确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinicopathological Features of 19 Eyelid Pilomatrixomas.

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Clinicopathological Features of 19 Eyelid Pilomatrixomas.

Introduction: Pilomatrixoma is a relatively rare, benign tumor arising from the hair root matrix. It is found frequently on the head and neck, with most involving the eyebrow in the periocular region. In contrast, eyelid pilomatrixoma is less common, and often clinically misdiagnosed. Here, we present clinical and histological data from 19 pilomatrixomas arising in the eyelid.

Methods: The study represents a retrospective study of eyelid pilomatrixoma diagnosed at our institution since 1981. All slides were reviewed, and demographic as well as clinical data were obtained.

Results: Patient ages ranged from 2 to 63 years (mean 24 years), including 12 (63%) females and 7 (37%) males. Eight (42%) and 4 (21%) cases arose in the first and second decades of life, respectively. Upper eyelid involvement was found in 14 (74%) of cases. Microscopically, the tumors were characterized by basaloid and shadow cells accompanied by calcification and foreign body giant cells.

Conclusions: Eyelid pilomatrixoma is rarely suspected clinically, and can be mistaken for cyst, chalazion, sebaceous carcinoma, and other tumors. Physicians should consider the possibility of pilomatrixoma in the eyelid area, especially in children or young female patients. Complete excision is curative, and diagnosis can generally be established by histopathological examination.

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