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Mucosa-Associated Lymphoid Tissue (MALT)-Type Malignant Lymphoma of the Stomach, Report of a Case Shin-ichiro Aozaki 1,3 , Kazuyuki Hagihara 2 , Kouichi Matsuno 3 , Kazuhisa Hasui 4 1Department of Internal Medicine, Saiseikai Sendai Hospital 2Department of Surgery, Saiseikai Sendai Hospital 3The Second Department of lnternal Medicine, Faculty of Medicine, Kagoshima University 4The Second Department of Pathology, Faculty of Medicine, Kagoshima University Keyword: 胃悪性リンパ腫 , MALTリンパ腫 , RLH , 低悪性度B細胞性リンパ腫 pp.1115-1123
Published Date 1993/9/25
DOI https://doi.org/10.11477/mf.1403106271
  • Abstract
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 Endoscopic examination was carried out in a 72-year-old female for small elevated lesions in the upper body and angular region of her stomach which were indicated by medical checkup-gastric roentgenography. She had no subjective symptom. Low-grade malignant B-cell lymphoma of the stomach was diagnosed from the histology of the biopsied specimens.

 The detailed x-ray examination showed abnormal areae gastricae extending to the whole stomach. The abnormality of areae gastricae contained irregularity in size and form, and disorders of direction and arrangement. Sulcus-like erosions surrounding the individual areae gastricae were sporadically observed. Endoscopic examination showed unevenness of the mucosa distributing on the whole stomach. The mucosa was composed of variously sized and smooth-surfaced granules with sporadically distributed sulcus-like erosions which was revealed by dye spraying method.

 We then diagnosed as gastric malignant lymphoma of superficial spreading type. Total gastrectomy was subsequently performed for the patient.

 Examination of the whole stomach resected in the serial sections showed that malignant lymphoma (ML) cells revealed infiltrative proliferation with sporadic or diffuse growth pattern in the mucosa of the whole stomach and involved focally the submucosal layer. No metastasis of the ML was seen in the regional lymph nodes examined. The ML cells were small lymphocytic, comprising cytologically so-called centrocytoid cells, monocytoid cells and plasmacytoid cells. These ML cells formed lymphoepithelial lesions in the mucosa. Paraffin-immunohistochemically the ML cells were B cells and revealed differentiation to plasma cells having monoclonal cytoplasmic immunoglobulin. Thus, this case was diagnosed as mucosa-associated lymphoid tissue (MALT)-type malignant lymphoma involving almost whole mucosa of the stomach.


Copyright © 1993, 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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