单纯放疗治疗原发性十二指肠黏膜相关淋巴组织淋巴瘤。

IF 0.6 Q4 GASTROENTEROLOGY & HEPATOLOGY
Won-Jae Lee, Keon-Young Ma, Hyung-Hoon Oh, Yoo-Duk Choi, Young-Eun Joo
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引用次数: 0

摘要

原发性粘膜相关淋巴组织淋巴瘤(MALT)是一种罕见的非霍奇金淋巴瘤亚型,约占所有非霍奇金淋巴瘤的8%。原发性胃肠道MALT淋巴瘤通常发生在胃,但累及十二指肠极为罕见。因此,原发性十二指肠MALT淋巴瘤因其罕见,其临床表现、治疗及预后尚未得到证实。本文报告一例40岁男性原发性十二指肠MALT淋巴瘤,仅用放射治疗成功。一名40岁男子前来进行医疗检查。食管胃十二指肠镜检查显示十二指肠第二和第三段白色多结节性粘膜病变。十二指肠粘膜病变活检标本被报道为十二指肠MALT淋巴瘤的怀疑。他接受了15次总剂量为3000 cGy的外束放射治疗,持续了三周。放射治疗三个月后,内镜检查显示十二指肠病变完全消退。放疗后随访12个月未见肿瘤复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Duodenal Mucosa-associated Lymphoid Tissue Lymphoma Treated with Radiation Therapy Alone.

Primary mucosa-associated with a lymphoid tissue (MALT) lymphoma is a rare distinct subtype of non-Hodgkin's lymphoma that occurs in approximately 8% of all non-Hodgkin lymphomas. Primary gastrointestinal MALT lymphoma usually occurs in the stomach, but duodenal involvement is extremely rare. Therefore, the clinical manifestations, treatment, and prognosis of primary duodenal MALT lymphoma have not yet been validated because of its rarity. This paper reports a case of a 40-year-old male with primary duodenal MALT lymphoma who was treated successfully with radiation therapy alone. A 40-year-old male visited for a medical check-up. Esophagogastroduodenoscopy revealed whitish multi-nodular mucosal lesions in the second and third portions of the duodenum. Biopsy specimens from mucosal lesions in the duodenum were reported to be suspicious for MALT lymphoma of the duodenum. He received a total dose of 3,000 cGy in 15 fractions with external beam radiation therapy for three weeks. Three months after radiation therapy, an endoscopic examination revealed complete resolution of the duodenal lesions. The follow-up 12 months after radiation therapy showed no evidence of tumor recurrence.

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
83
审稿时长
24 weeks
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