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Primary Rectal Malignant Lymphoma, Report of a Case Hiroshi Kasahara 1 , Michio Kato 1 , Hiromoto Shiki 1 , Harumasa Ohyanagi 1 , Yoichi Saitoh 1 1The First Department of Surgery, Kobe University School of Medicine Keyword: 悪性リンパ腫 , 直腸原発性悪性リンパ腫 pp.687-692
Published Date 1991/6/25
DOI https://doi.org/10.11477/mf.1403102566
  • Abstract
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 A 63 year-old woman patient was admitted with bloody stool as her chief complaint. Digital examination revealed a rectal mass. Barium enema (Fig. 2) and colonoscopy (Fig. 3) revealed a tumor of the rectum. Its endoscopic findings were suggestive of malignant lymphoma, although the biopsy specimen revealed no tumor cells. Under a clinical diagnosis of a malignant lymphoma of the rectum, a sphincter-saving operation with end-to-end anastomosis was performed. The tumor was limited to the rectum without any metastasis in the liver, spleen and retroperitoneal cavity. In the resected specimen the lesion, 3.5×1.2 cm in diameter, was located in the rectum (Fig. 4). In histologic examination, the most distinctive feature of the tumor cells was the diffuse pattern of growth at low-power view (Fig. 5 a). Tumor cells were composed of small lymphoid cells. Mitoses were found occasionally at high-power view (Fig. 5 b). Immunoperoxidase studies demonstrated the monoclonal B cell origin of these cells (LCA(+), L 26(+), MT 1(-), Ki-1(-)) (Fig. 6).

 Using these findings, this tumor was diagnosed as primary rectal malignant lymphoma, diffuse mixed-cell type (classification of Japan Lymphoma-Leukemia Study Group; LSG), stage Ⅰ.


Copyright © 1991, 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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