含骨的上唇复发性绒毛膜瘤:病例报告和分类细读。

IF 0.5 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmology Pub Date : 2024-05-08 eCollection Date: 2024-01-01 DOI:10.1159/000538824
Zachary George Angus, Penelope McKelvie, Thomas G Hardy
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引用次数: 0

摘要

简介上腔静脉瘤是一种先天性良性病变,在异常的异位位置含有组织学上看起来正常的组织。根据组织学检查结果,上腔静脉瘤可分为上皮样瘤、真皮脂肪瘤或复合静脉瘤。本病例推测为上皮脂瘤,影像学、检查或术中均未发现骨化迹象,直到对标本进行组织学检查,才明确病变为上皮脂瘤复合绒毛膜瘤。令人欣慰的是,此类病变中出现骨化并不会改变治疗方案:一位母亲发现她 9 岁女儿的颞上球结膜上有一个小的肉质肿块。经核磁共振成像确认为上皮脂瘤,最初采取保守治疗。两年后,她因明显增生和美容问题转诊,并接受了手术切除:结论:我们介绍的这个病例具有不寻常的表现和组织学发现。眼眶外科医生应注意上睑绒毛膜瘤骨化的可能性,避免与其他诊断相混淆。本文对上睑脉管瘤的最新分类系统进行了澄清。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epibulbar Complex Choristoma Containing Bone: A Case Report and Closer Look at Classifications.

Introduction: Epibulbar choristoma is a benign congenital lesion containing histologically normal-appearing tissue in an abnormal ectopic location. An epibulbar choristoma is classified as either epibulbar dermoid, dermolipoma, or complex choristoma based on histological examination. The case presented was a presumed epibulbar dermolipoma with no signs of ossification on imaging, examination, or intraoperatively until the specimen was examined histologically, clarifying the lesion as an epibulbar complex choristoma. Reassuringly, the presence of bone in such lesions should not change management.

Case presentation: A mother noticed a small fleshy mass on her 9-year-old daughter's superotemporal bulbar conjunctiva. The suspected epibulbar dermolipoma was confirmed with MRI and initially managed conservatively. Two years later, she was referred for apparent growth and cosmetic concerns, and she underwent surgical debulking.

Conclusion: We present this case for its unusual presentation and histological findings. Orbital surgeons should be aware of the possibility of ossification of epibulbar choristomas and avoid confusion with alternative diagnoses. Clarification of the latest classification system for epibulbar choristomas is provided.

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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
129
审稿时长
12 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of ophthalmology, including prevention, diagnosis, treatment, toxicities of therapy, supportive care, quality-of-life, and survivorship issues. The submission of negative results is strongly encouraged. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed. The intent of the journal is to provide clinicians and researchers with a tool to disseminate their personal experiences to a wider public as well as to review interesting cases encountered by colleagues all over the world. Universally used terms can be searched across the entire growing collection of case reports, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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