Fan Jennifer C, Lamont Duncan L, Greenbaum Adam R, Ng Stephen G J
Department of Ophthalmology, Waikato Hospital, Waikato District Health Board, Hamilton, New Zealand.
Orbit. 2011 Dec;30(6):297-9. doi: 10.3109/01676830.2011.602170.
The authors describe a case of orbital extraskeletal osteosarcoma. A 78-year-old man with a history of rheumatoid arthritis on long-term corticosteroids had a left medial canthal basal cell carcinoma excision followed by adjuvant radiotherapy. Twelve months later, he re-presented with a large rapidly-growing calcified mass involving his left medial canthus and orbit. An incisional biopsy demonstrated an infiltrate of atypical cells exhibiting mitotic activity with a rosette arrangement around partially calcified necrotic tissue. The patient underwent orbital exenteration and a partial maxillectomy. Histopathology demonstrated an extraskeletal osteosarcoma. It is extremely rare for this tumor to occur in the orbit. Immunosuppression and adjuvant radiotherapy were possible predisposing factors in the development of this tumor. Extraskeletal osteosarcoma (ESOS) is a malignant tumour that produces osteoid. It develops in soft tissue without continuity to bone or periosteum. It is rare and comprises fewer than 5% of all osteosarcomas. Extraskeletal osteosarcoma primarily affects patients above 50 years of age and has a poor prognosis. In this report, we describe the clinical, radiologic, and pathologic records of a rare case of primary ESOS of the orbit.
作者描述了一例眼眶骨外骨肉瘤病例。一名78岁男性,有类风湿关节炎病史,长期服用皮质类固醇,曾接受左内眦基底细胞癌切除及辅助放疗。12个月后,他再次出现一个累及左内眦和眼眶的迅速增大的钙化肿块。切开活检显示非典型细胞浸润,有丝分裂活跃,围绕部分钙化坏死组织呈玫瑰花结样排列。患者接受了眼眶内容剜除术和部分上颌骨切除术。组织病理学显示为骨外骨肉瘤。这种肿瘤发生在眼眶极为罕见。免疫抑制和辅助放疗可能是该肿瘤发生的易感因素。骨外骨肉瘤(ESOS)是一种产生类骨质的恶性肿瘤。它发生于与骨或骨膜无连续性的软组织中。它很罕见,占所有骨肉瘤的比例不到5%。骨外骨肉瘤主要影响50岁以上的患者,预后较差。在本报告中,我们描述了一例罕见的眼眶原发性ESOS的临床、放射学和病理学记录。