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A Giant Polypoid Tumor of the Esophagus: A case report G. Asano 1 , N. Yamada 1 , K. Ishigami 1 , H. Maeda 2 , T. Hirakawa 2 , T. Taguchi 2 1Department of Pathology, Nippon Medical School 2Department of Internal Medicine, Nippon Medical School pp.1251-1255
Published Date 1977/9/25
DOI https://doi.org/10.11477/mf.1403112571
  • Abstract
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 A 69-year-old man was admitted to our hospital with complaints of dysphagia and vague discomfort in the back. Upper gastrointestinal X-ray series and endoscopic study demonstrated a giant, inoperable polypoid tumor at the middle third of the esophagus. Three months later he died from combined bronchopneumonia. Autopsy revealed a polypoid tumor measuring 10×3×4 cm.

 Histologically, the tumor showed infiltrating squamous cell carcinoma composed of basal cells and spindle cells, accompanied with atypical spindle cells and multinuclear giant cells. The presence of these atypical spindle cells was confirmed as sarcomatous transformation of carcinoma cells, because fibroblastappearing rough endoplasmic reticulum was observed in the cytoplasm by electron microscopic examination. This tumor may be diagnosed as follows ; collision tumor, carcinoma with pseudosarcoma, carcinoma with benign stromal tumor (so-called carcinosarcoma) and/or anaplastic carcinoma.

 For monogenetic interpretation of the tumor, those diagnoses seemed to present an inappropriate terminology for the carcinosarcoma. Therefore, the previously reported literature are reviewed and the differentiation between carcinosarcoma and pseudosarcoma is discussed.


Copyright © 1977, 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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