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淋巴瘤化疗后先天性肠淋巴管扩张症吸收不良的缓解

Remission of malabsorption in congenital intestinal lymphangiectasia following chemotherapy for lymphoma.

作者信息

Shpilberg O, Shimon I, Bujanover Y, Ben-Bassat I

机构信息

Institute of Hematology, Chaim Sheba Medical Center, Tel-Hashomer, Israel.

出版信息

Leuk Lymphoma. 1993 Sep;11(1-2):147-8. doi: 10.3109/10428199309054743.

DOI:10.3109/10428199309054743
PMID:8220148
Abstract

A 22-year-old female with protein losing enteropathy due to congenital intestinal lymphangiectasia who developed non-Hodgkin's lymphoma of the bone, is described. Complete remission of the lymphomatous process and disappearance of the gastrointestinal symptoms were achieved following treatment with combination chemotherapy and local irradiation.

摘要

本文描述了一名22岁患有先天性肠淋巴管扩张症所致蛋白丢失性肠病的女性,其罹患了骨非霍奇金淋巴瘤。联合化疗及局部放疗后,淋巴瘤病情完全缓解,胃肠道症状消失。

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引用本文的文献

1
A case of primary intestinal lymphangiectasia with non-Hodgkin lymphoma.原发性肠道淋巴管扩张症合并非霍奇金淋巴瘤 1 例
BMC Gastroenterol. 2021 Dec 11;21(1):461. doi: 10.1186/s12876-021-01997-x.
2
Deterioration of duodenal lymphangiectasia after radiotherapy for gastric MALT lymphoma.胃黏膜相关淋巴组织淋巴瘤放疗后十二指肠淋巴管扩张症的恶化
Ecancermedicalscience. 2017 Jul 11;11:752. doi: 10.3332/ecancer.2017.752. eCollection 2017.
3
Intestinal lymphangiectasia in adults.成人肠淋巴管扩张症。
World J Gastrointest Oncol. 2011 Feb 15;3(2):19-23. doi: 10.4251/wjgo.v3.i2.19.
4
Primary intestinal lymphangiectasia (Waldmann's disease).原发性肠淋巴管扩张症(瓦尔德曼病)。
Orphanet J Rare Dis. 2008 Feb 22;3:5. doi: 10.1186/1750-1172-3-5.