Primary Synovial Sarcoma of the Orbit.

Ophthalmology and eye diseases Pub Date : 2017-04-17 eCollection Date: 2017-01-01 DOI:10.1177/1179172117701732
Pei Xu, Jianbin Chen
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引用次数: 7

Abstract

Purpose: To describe the clinical, pathological, and immunohistochemical characteristics and therapies of a rare case of primary synovial sarcoma in the orbit.

Design: Retrospective interventional case report.

Participant: A 6-year-old girl with pathologically proven synovial sarcoma in the orbit. The diagnosis was confirmed by immunohistochemistry.

Methods: The patient was treated with right lateral orbital and right temporal tumor resection, followed by chemotherapy. She was followed up every 3 months for 1 year.

Results: The tumor was excised, and the patient received 5 courses of chemotherapy. She did well during the initial first-year follow-up with no recurrent signs.

Conclusions: We reported the sixth case of primary synovial sarcoma in the orbit and the first case of a 6-year-old girl.

Abstract Image

Abstract Image

Abstract Image

原发性眼眶滑膜肉瘤。
目的:描述一例罕见的眼眶原发性滑膜肉瘤的临床、病理、免疫组织化学特征及治疗方法。设计:回顾性介入病例报告。参与者:一名6岁女孩,病理证实眼眶滑膜肉瘤。免疫组织化学证实了诊断。方法:行右侧眶外侧及右侧颞部肿瘤切除术,并行化疗。每3个月随访1年。结果:肿瘤全部切除,化疗5个疗程。在最初的第一年随访中,患者表现良好,无复发症状。结论:我们报告了第6例眼眶原发性滑膜肉瘤,第一例为6岁女童。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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