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Lymphangioma Cavernosum of the Sigmoid Colon Associated with Borrmann Type 2 Gastric Cancer, Report of a Case Kazutami Kazato 1 1Kanagawa Prefectural Center for the Elderly's Diseases pp.229-236
Published Date 1988/2/25
DOI https://doi.org/10.11477/mf.1403107921
  • Abstract
  • Look Inside

 Lymphangioma rarely occurs in the colon. Forty such lesions in 39 patients have been reported in Japan, as of June, 1986.

 We report here 64 year-old man diagnosed by barium enema radiography as having Lymphangioma of the colon in addition to Borrmann type 2 gastric cancer. This was the second case in Japan in which biopsy specimen showed the tumor invading into m, sm, which was the clue to the diagnosis.

 Gross observation of the resected specimen revealed P3 smooth-surfaced tumor measuring 60 mm by 30 mm by 20 mm, with two raised areas compressible on pressure and pulsation in the ventral wall of the colon. Pathologically, proliferation of the thin-walled lymph vessels with small or large cystic dilatation was seen in the submucosal layer as well as in the lamina propria mucosae. Neoplastic proliferation of the endothelium, however, was not seen.

 Based on these findings, the diagnosis of Lymphangioma cavernosum was made.


Copyright © 1988, 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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