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102 gastroscopically taken biopsy specimens which were normal (n = 28) or showed superficial gastritis (n = 18), chronic atrophic gastritis (n = 18), gastric ulcers (n = 19) and gastric carcinomas (n = 19) were submitted to FCM analysis. Carcinomatous specimens were readily recognized by either ploidy abnormality or significantly raised S- and G2 + M values. Intestinal-type and diffuse carcinomas could not be distinguished by proliferation kinetics, however, diffuse carcinomas showed a higher rate of aneuploidy. Chronic atrophic gastritis and gastric ulcers, though significantly differing from both normal tissue and superficial gastritis, exhibited similar proliferation characteristics. In gastric ulcers, an S-phase proportion of more than 12% was correlated with histological detection of cellular atypias and a proliferative tendency.
E Deinlein, and
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R Grässel-Pietrusky, and
O P Hornstein
January 1986,
Virchows Archiv. B, Cell pathology including molecular pathology,
E Deinlein, and
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O P Hornstein
December 1987,
Scandinavian journal of gastroenterology,
E Deinlein, and
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O P Hornstein
January 1992,
Anticancer research,
E Deinlein, and
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August 1988,
World journal of surgery,
E Deinlein, and
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July 1989,
Gan no rinsho. Japan journal of cancer clinics,
E Deinlein, and
H Schmidt, and
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O P Hornstein
December 1987,
Analytical and quantitative cytology and histology,
E Deinlein, and
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O P Hornstein
January 1986,
Acta dermato-venereologica. Supplementum,
E Deinlein, and
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O P Hornstein
January 1982,
Virchows Archiv. A, Pathological anatomy and histopathology,
E Deinlein, and
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R Grässel-Pietrusky, and
O P Hornstein
August 1987,
Scandinavian journal of gastroenterology,
E Deinlein, and
H Schmidt, and
J F Riemann, and
R Grässel-Pietrusky, and
O P Hornstein
January 2021,
Endokrynologia Polska,
