de Maeyer V M D S, Kestelyn P A F A, Shah Akash D, Van Den Broecke C M, Denys H G N, Decock C E
Department of Ophthalmology, Ghent University Hospital, Ghent, Belgium.
Department of Orbit and Oculoplasty, Bombay City Eye Hospital, Mumbai, India.
Indian J Ophthalmol. 2016 Sep;64(9):687-689. doi: 10.4103/0301-4738.97555.
Primary extraskeletal osteosarcoma (EOS) is an extremely rare malignancy. In this report, the clinical course of a 32-year-old man presenting with proptoses is described. Medical history included Hirschsprung disease (HD), horseshoe kidney, azoospermia, and vertebral anomalies. Imaging of the orbit showed an oval, well-defined heterogeneous mass adjacent to the lateral wall of the orbit. The patient underwent a lateral orbitotomy and complete excision of the mass. The mass was not attached to the bone. Histopathologic and immunohistochemical examination confirmed the diagnosis of an EOS. The patient received chemotherapy and radiotherapy and is free of the disease 3 years after the diagnosis. Genetic screening showed no mutations for both the RET proto-oncogene for HD and the p53 tumor suppressor gene for osteosarcoma.
原发性骨外骨肉瘤(EOS)是一种极其罕见的恶性肿瘤。在本报告中,描述了一名32岁出现眼球突出男性的临床病程。病史包括先天性巨结肠病(HD)、马蹄肾、无精子症和椎体异常。眼眶影像学检查显示在眼眶外侧壁附近有一个椭圆形、边界清晰的不均匀肿块。患者接受了外侧眼眶切开术并完整切除了肿块。肿块未附着于骨骼。组织病理学和免疫组化检查确诊为EOS。患者接受了化疗和放疗,诊断后3年无疾病复发。基因筛查显示HD相关的RET原癌基因和骨肉瘤相关的p53肿瘤抑制基因均无突变。