跟骨单中心上皮样血管内皮瘤1例报告及文献复习。

Clinical Sarcoma Research Pub Date : 2018-04-06 eCollection Date: 2018-01-01 DOI:10.1186/s13569-018-0092-z
Mark C Plumby, Patrick Bacaj, Brock A Lindsey
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引用次数: 5

摘要

背景:本文结合一个临床病例对文献进行回顾,阐述了这种可变的低级别恶性肿瘤的良好预后,显示了保留肢体手术与病灶内治疗的作用,并提供了一种罕见的恶性肿瘤上皮样血管内皮瘤的临床例子。病例报告:病例报告提出一例孤立上皮样血管内皮瘤(EHE)的跟骨在60岁的男性。骨的原发性血管肿瘤是罕见的;然而,EHE是骨中最常见的原发性恶性血管肿瘤之一。回顾文献发现很少有病例涉及跟骨;这些病例发现累及跟骨是多灶性或转移性疾病过程的一部分。我们的病例提出了一个45个月的临床随访孤立EHE在跟骨通过刮除和水泥手术切除治疗。结论:该病例术后临床随访时间超过2年,可作为一种罕见疾病的治疗指南,但文献较少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Unicentric epithelioid hemangioendothelioma of the calcaneus: a case report and review of literature.

Background: This review of the literature combined with a clinical case will allow the illustration of a favorable outcome of this variable low grade malignancy, display a role for limb salvage surgery with intralesional treatment, and offer a clinical example of epithelioid hemangioendothelioma, a rare malignancy.

Case presentation: The case report presents a case of solitary epithelioid hemangioendothelioma (EHE) of the calcaneus in a 60-year-old male. Primary vascular tumors of the bone are rare; however, EHE is one of the most common primary malignant vascular tumors to occur in bone. A review of the literature found few cases that involved the calcaneus; those cases found that involved the calcaneus were either part of a multifocal or metastatic disease process. Our case presents a 45-month clinical follow-up of solitary EHE in the calcaneus treated with surgical excision by curettage and cementing.

Conclusion: This case has clinical follow-up greater than 2 years post-operatively and could be a guide for treatment of a rare disorder with a substantial paucity of literature.

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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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