Furrukh Muhammad, Qureshi Asim, Mamoon Nadira, Fatima Menahil
Radiation Oncology, Shifa Internal Hospital, Islamabad, Pakistan.
Pathology, Shifa International Hospital, Islamabad, Pakistan.
BMJ Case Rep. 2017 Jun 22;2017:bcr-2017-219722. doi: 10.1136/bcr-2017-219722.
Extraskeletal osteosarcomas (OSs) are highly malignant soft tissue tumours associated with a poor prognosis. Only a few records of these rare aggressive neoplasms have been reported in the literature.We describe the case of a 49-year-old man, who presented to our tertiary care centre with a painful isolated lump around the umbilicus. After surgical biopsy, imaging and subsequent pathological analysis, the swelling was diagnosed to be a localised extraskeletal OS. He received previous radiation as treatment for testicular seminoma 40 years ago, which has been in remission ever since. He also happens to have testicular hydrocele since 10 years. He was subjected to resection and free flap reconstruction complicated by lower anterior abdominal wall haematoma and large pseudoaneurysm of the left femoral artery. Patient completed 60 Gy of adjuvant electron beam irradiation for close margins and is scheduled for adjuvant chemotherapy. We describe a brief account of his illness.
骨外骨肉瘤(OS)是一种高度恶性的软组织肿瘤,预后较差。文献中仅报道了少数关于这些罕见侵袭性肿瘤的记录。我们描述了一名49岁男性的病例,他因脐周出现疼痛性孤立肿块前来我们的三级护理中心就诊。经过手术活检、影像学检查及后续病理分析,该肿胀被诊断为局限性骨外骨肉瘤。他40年前曾接受放疗以治疗睾丸精原细胞瘤,此后一直处于缓解期。他还患有睾丸鞘膜积液10年。他接受了切除及游离皮瓣重建手术,术后出现下腹部前壁血肿和左股动脉大假性动脉瘤等并发症。患者因切缘阳性完成了60 Gy的辅助电子束照射,并计划接受辅助化疗。我们简要描述了他的病情。