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双侧卵巢伯基特淋巴瘤：1例威廉姆斯综合征患儿的病例报告

Bilateral burkitt lymphoma of the ovaries: a report of a case in a child with williams syndrome.

作者信息

Onimoe Grace Ifeyinwa, Kahwash Samir, Termuhlen Amanda, Gross Thomas G, Varga Elizabeth, Rose Melissa J

机构信息

Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Case Rep Med. 2011;2011:327263. doi: 10.1155/2011/327263. Epub 2011 May 26.

DOI:10.1155/2011/327263
PMID:21687537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3114539/
Abstract

A 10-year-old female with Williams Syndrome (WS) presented with a two-month history of fatigue, weight loss, and bilateral ovarian masses. Histologic, immunophenotypic, and cytogenetic studies confirmed the diagnosis of Burkitt lymphoma (BL). While there is no established association between the two disorders, this is the third case in the literature of Burkitt lymphoma in a patient with Williams Syndrome.

摘要

一名患有威廉姆斯综合征（WS）的10岁女性，出现疲劳、体重减轻和双侧卵巢肿块2个月的病史。组织学、免疫表型和细胞遗传学研究证实为伯基特淋巴瘤（BL）。虽然这两种疾病之间尚无既定关联，但这是文献中第三例威廉姆斯综合征患者发生伯基特淋巴瘤的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b25/3114539/fdd53b952323/CRIM2011-327263.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b25/3114539/66a2675e7bc8/CRIM2011-327263.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b25/3114539/fdd53b952323/CRIM2011-327263.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b25/3114539/66a2675e7bc8/CRIM2011-327263.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b25/3114539/fdd53b952323/CRIM2011-327263.002.jpg

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