眼眶纤维组织细胞瘤1例报告并文献复习。

T K Ulloa, S F Anderson
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引用次数: 0

摘要

背景:纤维组织细胞瘤是一组不同的软组织肿瘤,组织学上分为良性、局部侵袭性和恶性。这些肿瘤遍布全身,但似乎对眶周区域有亲和力。它们占所有眼部肿块的1%,是眼眶最常见的原发性间充质肿瘤。相关的眼部体征和症状包括视力下降、眼球突出、复视、疼痛、眼外肌运动受限、眼睑和结膜肿胀以及眼盘水肿。病例报告:报告一例良性眼眶纤维组织细胞瘤。患者报告间歇性疼痛和偶尔复视;右上眼睑严重水肿;观察右眼球突出及下垂直位移。计算机断层扫描显示一个明确的肿块,随后手术切除,武装部队病理研究所的组织病理学结果证实了诊断。结论:眼眶纤维组织细胞瘤是一种罕见的眼周肿瘤,可表现多种眼部体征和症状。仔细的组织学检查对诊断是必要的,因为这些肿瘤具有广泛的形态。鉴别诊断包括有相似放射学或组织学表现的眼眶肿块。
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Orbital fibrous histiocytoma: case report and literature review.

Background: Fibrous histiocytomas are a diverse group of soft tissue tumors classified histiologically as benign, locally aggressive, and malignant. These tumors are found throughout the body, but seem to have an affinity for the periorbital area. They account for one percent of all ocular masses and are the most common primary mesenchymal tumor of the orbit. Associated ocular signs and symptoms include decreased visual acuity, proptosis, diplopia, pain, restricted extraocular muscle movement, swelling of the eyelids, and conjunctiva, as well as disk edema.

Case report: A case of a benign orbital fibrous histiocytoma is presented. The patient reported intermittent pain and occasional diplopia; severe edema of the right upper eyelid; and proptosis and inferior vertical displacement of the right globe were observed. Computed tomography revealed a well-defined mass that was subsequently surgically removed and histopathological results from the Armed-Forces Pathology Institute confirmed the diagnosis.

Conclusions: Orbital fibrous histiocytomas are rare periocular tumors that can manifest multiple ocular signs and symptoms. Careful histologic examination is necessary for diagnosis, since these tumors have a wide range of morphology. Differential diagnoses include orbital masses with similar radiologic or histologic findings.

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