意想不到的淋巴瘤罕见的原发性胃伯基特淋巴瘤病例。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL

Journal of investigative medicine high impact case reports Pub Date : 2024-01-01 DOI:10.1177/23247096241253341

Jonathan London, Sabrina Bulancea, Sharnjyot Wander, Shirley Ponnaiya, Leilah Tisheh, Sanjeev Jain, Prakash Viswanathan, Zubin Tharayil

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引用次数: 0

摘要

原发性胃伯基特淋巴瘤是一种侵袭性非霍奇金淋巴瘤，在文献中鲜有报道。原发性胃伯基特淋巴瘤大多为弥漫大B细胞淋巴瘤和粘膜相关淋巴组织（MALT）淋巴瘤。原发性胃伯基特淋巴瘤患者可表现为腹痛、吐血、黑便、穿孔和梗阻。诊断需要结合临床、放射学和病理学检查结果。由于报道的病例有限，治疗数据也很有限。我们报告了一例 47 岁女性的病例，她出现弥漫性腹痛、化脓性腹泻和咖啡样呕吐，在上内镜检查中发现胃溃疡肿块，活检后诊断为原发性胃伯基特淋巴瘤。

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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An Unexpected Lymphoma: A Rare Case of Primary Gastric Burkitt's Lymphoma.

Primary gastric Burkitt's lymphoma is an aggressive non-Hodgkin's lymphoma that has been rarely reported in the literature. The majority of primary gastric lymphomas are diffuse large B-cell lymphomas and mucosa-associated lymphoid tissue (MALT) lymphomas. Patients with primary gastric Burkitt's lymphoma can present with abdominal pain, hematemesis, melena, perforation, and obstruction. Diagnosis is made with a combination of clinical, radiological, and pathological findings. Treatment data are limited due to the limited cases reported. We present a case of a 47-year-old female who presented with diffuse abdominal pain, melena, and coffee-ground emesis that was diagnosed with primary gastric Burkitt's lymphoma following biopsies taken from a gastric ulcerated mass found on upper endoscopy.

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来源期刊

Journal of investigative medicine high impact case reports MEDICINE, GENERAL & INTERNAL-

CiteScore

1.90

自引率

0.00%

发文量

165

审稿时长

12 weeks

期刊介绍： The AFMR is committed to enhancing the training and career development of our members and to furthering its mission to facilitate the conduct of research to improve medical care. Case reports represent an important avenue for trainees (interns, residents, and fellows) and early-stage faculty to demonstrate productive, scholarly activity.