Suppr超能文献

跟骨原发性上皮样血管肉瘤:诊断难题

Primary epithelioid angiosarcoma of the calcaneum: a diagnostic dilemma.

作者信息

Balaji Gopisankar G, Arockiaraj Justin S V, Roy Alfred Cyril, Deepak Burad

机构信息

Assistant Professor in Orthopaedics, Department of Orthopaedics, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.

Assistant Professor in Orthopaedics, Department of Orthopaedics Unit 1, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

J Foot Ankle Surg. 2014 Mar-Apr;53(2):239-42. doi: 10.1053/j.jfas.2013.10.010. Epub 2013 Dec 19.

Abstract

Primary epithelioid angiosarcoma of the bone is very rare. We report a rare case of epithelioid angiosarcoma of the calcaneum and the difficulties we had in diagnosing this condition. A 22-year-old woman presented with complaints of pain and swelling of the left ankle of 8 years' duration. Examination revealed swelling and tenderness over the lateral aspect of calcaneum. Plain radiographs showed an osteolytic lesion of the calcaneum. She underwent curettage and bone grafting, with bone substitutes. Histopathologic examination showed epithelioid angiosarcoma in contrast to the needle biopsy, which had showed an aneurysmal bone cyst. The patient was counseled about the need for amputation. She refused limb ablative surgery, and the likelihood of local recurrence and systemic spread and the need for close follow-up were explained. At the end of 3 years of follow-up, she was pain free and had no evidence of recurrence. We present this case because of the rare site, histopathologic challenges in diagnosing the condition, and unique presentation of the disease.

摘要

原发性骨上皮样血管肉瘤非常罕见。我们报告一例罕见的跟骨上皮样血管肉瘤病例以及诊断该疾病时遇到的困难。一名22岁女性,主诉左踝疼痛肿胀8年。检查发现跟骨外侧肿胀、压痛。X线平片显示跟骨有溶骨性病变。她接受了刮除术及骨移植,使用了骨替代物。组织病理学检查显示为上皮样血管肉瘤,而针吸活检显示为动脉瘤样骨囊肿。已告知患者截肢的必要性。她拒绝肢体切除手术,并向其解释了局部复发和全身转移的可能性以及密切随访的必要性。随访3年结束时,她无疼痛,且无复发迹象。我们展示此病例是因为其发病部位罕见、诊断时存在组织病理学挑战以及该疾病的独特表现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验