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Giant Cell Carcinoma of the Stomach, Report of a Case Eiji Kanehira 1 , Masaaki Nakagawa 1 , Morimoto Hayashi 2 , Youichi Kawamura 3 1Department of General Surgery, Ishikawa Prefectural Central Hospital 2Department of Histopathology, Ishikawa Prefectural Central Hospital 3Department of Hematology, Ishikawa Prefectural Central Hospital pp.455-460
Published Date 1989/4/25
DOI https://doi.org/10.11477/mf.1403106441
  • Abstract
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 The patient, a 51-year-old female was referred to our hospital because of epigastric discomfort. Upper gastrointestinal series and gastric endoscopy revealed a large Borrmann's Type-1 tumor extending from the cardia to the fornix (Figs. 1 a, 1 b and 2).

 Since the operative findings indicated “H0P0S2N1”, total gastrectomy with R2-lymph node dissection was carried out.

 Histological findings revealed that the tumor was composed mainly of mufti-nucleated giant cells ranging from 40 to 80 μm in diameter, without any cellular differentiation. Stains for mucin were negative. This histological study led to a diagnosis of giant cell carcinoma of the stomach (Figs. 3 and 4).

 The patient, however, began to suffer from multiple liver metastasis and carcinomatous pleuritis only two months after the operation. This was followed by multiple organ failure and rapid deterioration culminating in death.

 Another factor in this case was the presence of marked leukocytosis which varied in direct proportion to the volume of the tumor. However, no “colony stimulating factor” could be detected from the tumor tissue.

 Up to now, only three cases, including ours, have been reported as giant cell carcinoma of the stomach.


Copyright © 1989, 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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