Clinicopathological Features of 19 Eyelid Pilomatrixomas.

Pub Date : 2022-02-01 DOI:10.1159/000520219
Sepideh Siadati, Ashley A Campbell, Timothy McCulley, Charles G Eberhart
{"title":"Clinicopathological Features of 19 Eyelid Pilomatrixomas.","authors":"Sepideh Siadati,&nbsp;Ashley A Campbell,&nbsp;Timothy McCulley,&nbsp;Charles G Eberhart","doi":"10.1159/000520219","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":0,"journal":{"name":"","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914276/pdf/oop-0008-0030.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000520219","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

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.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
眼睑毛基质瘤19例临床病理特征分析。
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。
求助全文
约1分钟内获得全文 去求助
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1