1例12岁女童原发性卵巢血管肉瘤:在资源有限的国家中罕见的局部病例报告。

Q2 Medicine

BMC Clinical Pathology Pub Date : 2017-08-24 eCollection Date: 2017-01-01 DOI:10.1186/s12907-017-0056-x

Tchin Darré, Abdoul-Samadou Aboubakari, Bingo K N'Bortche, Akila Bassowa, Solange Adani-Ifé, Gado Napo-Koura

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引用次数: 5

摘要

背景:卵巢肉瘤占所有卵巢癌的不到1%，通常常见于成人。原发性血管肉瘤在儿童卵巢中是罕见的。病例介绍:我们报告了一例原发性卵巢血管肉瘤的12岁女孩在资源有限的情况下。免疫组化结果显示CD34、CD31、因子VIII阳性，S100阴性。保留原发非转移性血管肉瘤的诊断。她无法接受CWS-2002P化疗，因为她的父母负担不起。结论:本病例报告描述了一个罕见类型的原发性卵巢血管肉瘤的儿童，诊断在一个低收入国家的实验室有限的资源。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Primary ovarian angiosarcoma in a 12- year -old girl: a case report of an exceptional localization in a context of limited resources country.

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Primary ovarian angiosarcoma in a 12- year -old girl: a case report of an exceptional localization in a context of limited resources country.

Background: Ovarian sarcomas represent less than 1% of all ovary cancers and usually are frequent in adults. Primary angiosarcomas are exceptional in the ovaries within children.

Case presentation: We reported a case of primary ovarian angiosarcoma in a 12-year-old girl in a resource-constrained context. Immunohistochemistry study showed the positivity of CD34, CD31, factor VIII, while S100 was negative. The diagnosis of primary non-metastatic angiosarcoma was retained. She was unable to undergo the CWS-2002P chemotherapy since her parents could not afford it.

Conclusion: This case report described a rare type of a primary ovarian angiosarcoma within a child, diagnosed in a low-income country in a laboratory with limited resources.

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来源期刊

BMC Clinical Pathology Medicine-Pathology and Forensic Medicine

CiteScore

3.30

自引率

0.00%

发文量

期刊介绍： BMC Clinical Pathology is an open access journal publishing original peer-reviewed research articles in all aspects of histopathology, haematology, clinical biochemistry, and medical microbiology (including virology, parasitology, and infection control). BMC Clinical Pathology (ISSN 1472-6890) is indexed/tracked/covered by PubMed, CAS, EMBASE, Scopus and Google Scholar.