An Uncommon Orbital Neoplasm: Solitary Fibrous Tumor: Case Report

O. Toygar, Levent Akçay, Özge Yabaş Kiziloğlu, Baha Toygar, Ö. Yapıcıer, M. Demir
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Abstract

The purpose of this case report is to present an intraconally located orbital solitary fibrous tumor, an uncommon fibroblastic tumor of the orbit which has diagnostic challenges. A 33 years old female patient presented with three years of slowly progressive mass and proptosis of the left eye. Magnetic resonance imaging demonstrated a well-defined, strongly enhancing intraconal orbital mass. Histopathological and immunohistochemical analysis following en bloc removal of the lesion revealed a mesenchymal tumor showing strong positivity for CD34 and Vimentin. The diagnosis was solitary fibrous tumor. Although uncommon, solitary fibrous tumor should be kept in mind in the differential diagnosis of a well-defined orbital mass associated with slowly progressive proptosis.
罕见眼眶肿瘤:孤立性纤维性肿瘤1例
本病例报告的目的是报告一个位于眶内的孤立性纤维性肿瘤,这是一种罕见的眼眶纤维母细胞肿瘤,具有诊断上的挑战。一位33岁的女性患者,以三年缓慢进展的肿块和左眼突出为主诉。磁共振成像显示一清晰、强化的眶内肿块。病灶整体切除后的组织病理学和免疫组织化学分析显示,间充质肿瘤显示CD34和Vimentin强烈阳性。诊断为孤立性纤维性肿瘤。虽然少见,但在鉴别诊断明确的眼眶肿块伴缓慢进展性突出时应注意孤立性纤维性肿瘤。
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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