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Lymphomatoid Granulomatosis with Gastric Involvement, Report of a Case Tsutomu Ishida 1 , Setsuko Hirai 1 , Hideyuki Hirai 1 , Akira Suzuki 1 , Takashi Minase 4 1The Third Department of Internal Medicine, Sapporp Medical College 4The Second Department of Pathology, Sapporo Medical College pp.1141-1147
Published Date 1985/10/25
DOI https://doi.org/10.11477/mf.1403109740
  • Abstract
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 Lymphomatoid granulomatosis (LYG) is a rare disease in Japan. It may predominantly involve the lung, the skin, the central and peripheral nervous system, the kidneys and other organs in various degrees. GI tract involvement, especially gastric lesions, however, is quite rare. We report here a case of LYG with gastric involvement which has been followed radiographically and endoscopically for two years and nine months.

 The patient, a 60-year-old man was admitted to our hospital complaining of weight loss in June 1981. Examinations showed multiple coin lesions in both sides of the lung, multiple interrupted gastric lesions, peripheral polyneuropathy, skin lesions, and a tumor in the left kidney. The diagnosis of LYG was made from the biopsy specimens from the lung, stomach and skin.

 With regard to the gastric involvement of LYG, only two cases of an operated ulcerative lesion have been reported to date. Our case, however, showed multiple, interrupted and diversified lesions which had an mixed ulcerative, polypoid and infiltrative appearance, and this resembled that of malignant lymphoma.

 The patient showed marked improvement for sometime on PDN and CPA therapy, but relapsed with gastric elevated lesion in May 1983. In March 1984, there were multiple coin lesions in the lung and multiple elevated lesions in the stomach. At present he is being kept under careful observation with PDN and CPA therapy.


Copyright © 1985, 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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