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小儿原发性脾血管肉瘤:一种针对罕见恶性肿瘤的积极多学科肿瘤管理方法。

Pediatric primary splenic angiosarcoma: an aggressive multidisciplinary approach to the oncologic management of a rare malignancy.

作者信息

Serrano Oscar K, Knapp Esther, Huang Kevin, Baran Galina, Statter Mindy, McClain Danielle, Gill Jonathan

机构信息

Division of Pediatric Surgery, Department of Surgery, Children's Hospital at Montefiore Medical Center, 3415 Bainbridge Avenue, New York, NY 10467, USA.

出版信息

World J Surg Oncol. 2014 Dec 9;12:379. doi: 10.1186/1477-7819-12-379.

Abstract

Primary splenic angiosarcoma is an extremely rare and aggressive neoplasm of the vasculature. Uniformly, primary splenic angiosarcoma is a fatal disease despite early diagnosis and treatment. Only patients with localized disease amenable to surgical resection achieve long-term, disease-free survival. We present a review of the literature and report a case of a 3-year-old girl with metastatic primary splenic angiosarcoma who was offered aggressive surgical and medical treatment with curative intent despite her advanced presentation.

摘要

原发性脾血管肉瘤是一种极其罕见且侵袭性强的血管肿瘤。一致的是,原发性脾血管肉瘤是一种致命疾病,尽管能早期诊断和治疗。只有局限性疾病且适合手术切除的患者才能实现长期无病生存。我们对文献进行了综述,并报告了一例3岁转移性原发性脾血管肉瘤女孩的病例,尽管其病情已属晚期,但仍对其进行了积极的手术和药物治疗,以期治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ee5/4295483/d9b1ba7f5392/12957_2014_1851_Fig1_HTML.jpg

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