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Localized Rectal Mucosa-associated Lymphoid Tissue (MALT) Lymphoma which Regressed after Radiation Therapy, Report of a Case Haruaki Shirakawa 1 , Taiji Akamatsu 2 , Syuichi Yokosawa 1 , Yasunori Kaneko 1 , Katsuaki Inoue 1,2 , Kei Kitahara 1 , Kenichi Suzawa 1 , Yayoi Ozaki 1 , Norikazu Arakura 1 , Hiroyoshi Ota 3 , Shigeru Sasaki 4 , Kendou Kiyosawa 1 1Internal Medicine, Gastroenterology, Shinsyu University School of Medicine 2Department of Endscopy, Shinshu University Hospital 3Department of Biomedical Sciences, School of Health Sciences, Shinshu University School of Medicine 4Department of Radiology, Shinshu University Hospital Keyword: 直腸 , MALTリンパ腫 , 放射線療法 pp.372-377
Published Date 2006/3/25
DOI https://doi.org/10.11477/mf.1403100293

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 A 56-year-old woman was referred to our hospital in August, 2004 for further examination of rectal tumors. The first colonoscopy revealed two elevated lesions ; one was a sessile elevated lesion (25mm in size) with nodular surface in the upper rectum, and the other was a small elevated lesion (10mm in size) in the lower rectum. Endoscopic ultrasonography showed thick hypoechoic change within the second layer. Histological finding of conventional biopsy could not definitively distinguish whether it was MALT lymphoma or reactive lymphoid hyperplasia. Jumbo biopsy using endoscopic mucosal resection (2 channel method) was performed for the sessile elevated lesion, and histological findings of it revealed infiltration of atypical lymphoid cells such as centrocyte-like cells in the mucosa and the submucosa. Immunohistochemical study showed that atypical lymphocytes were positive for CD20, and negative for CD3, CD5, and cyclin D1. The monoclonality of B-cells was not detected by polymerase chain reaction products for immunoglobulin heavy chain. Bone marrow examination and some imaging procedures revealed no other infiltration of lymphoma cells except at the rectum. From these findings, this patient was diagnosed as stage I rectal MALT lymphoma. Helicobacter pylori (H. pylori) was not detected in histology or culture of the patients gastric biopsy specimens. After obtaining adequately informed consent, antibiotic therapy using Levofloxacin (3×100mg/day) was administered for 7 days. However, no remarkable regression was recognized in the endoscopic and histological findings. After that, she was administered 30 Gy radiation therapy for the rectal lesion. No remarkable adverse effect except slight leukopenia was recognized. Colonoscopy after radiation therapy revealed remarkable regression of the rectal MALT lymphoma, and typical lymphoma cells had disappeared in the biopsy specimens. She has had no recurrence in the 12 months since radiation therapy.

 Radiation therapy is thought to be a useful therapeutic procedure for localized rectal MALT lymphoma as it is also for localized gastric MALT lymphoma without H. pylori infection or with resistance against eradication therapy for H. Pylori.


Copyright © 2006, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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