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Gastric Malignant Lymphoma which Progressed Rapidly from Superficial Ulcerative Type of Gastric Malignant Lymphoma (MALT Lymphoma), Report of a Case Satoshi Takemura 1,2 , Kenshi Yao 1 , Tsuneyoshi Yao 1 1Department of Gastroenterology, Fukuoka University Chikushi Hospital Keyword: 胃悪性リンパ腫 , Helicobacter pgtori , 除菌 pp.987-994
Published Date 1996/7/25
DOI https://doi.org/10.11477/mf.1403104194
  • Abstract
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 A 64-year-old man, visited our hospital in August, 1988 with a 7-year history of gastric ulcer and occasional nausea at night. Endoscopic study of the stomach revealed multiple gastric ulcer scars. The patient was followed up as a gastric ulcer case for seven years. In July, 1994, endoscopy was performed and demostrated granular mucosa, and multiple small ulcerative lesions on the anterior wall of the gastric angle. Histology of the biopsy of the specimens showed no evidence of malignant change. In November, 1994, the endoscopic picture revealed depressed lesions with ulcerative change on the anterior wall of the gastric angle and antrum. Histology of the biopsy of the sections revealed proliferation of atypical large lymphoid cells in the gastric mucosa. The diagnosis of MALT (mucosaassociated lymphoid tissue) lymphoma was suggested.

 Helicobacter pylori was detected by both culture and rapid urease test using biopsy samples, so we tried antibiotic therapy for H. pylori. After treatment, endoscopic and radiographical findings became partially worse. In March, 1995, the patient was admitted to our hospital, and partial gastrectomy was performed in March, 1995. Macroscopic findings of the resected stomach showed a 4.0 × 4.0 cm ulcerating tumor on the anterior wall of the gastric angle and in the follow-up period, the lesions that had been detected in the antrum and lower body had disapperaed. Histologic study revealed diffuse, large-cell type malignant lymphoma invading as far as the proper muscle layer.

 This case showed that, in a short period of time after eradication of Helicobacter pylori, the tumor partially multiplied radically and partially disappeared.

 There has been no report of cases resembling the unique clinical course of this case.


Copyright © 1996, 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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