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Research ArticleExperimental Studies

The Histogenesis of the Third Pathway of Colonic Carcinogenesis in Rats

CARLOS A. RUBIO
Anticancer Research March 2017, 37 (3) 1039-1042;
CARLOS A. RUBIO
Gastrointestinal and Liver Research Laboratory, Department of Pathology, Karolinska Institute and University Hospital, Stockholm, Sweden
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  • For correspondence: Carlos.Rubio@ki.se
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    Figure 1.

    Histological features in colon tissue from dimethylhydrazine-treated Sprague-Dawley rats. Upper panel: Corrupted crypts with asymmetric fission (a, b) or aberrant crypt alignment (c, arrow) in colonic gut-associated lymphoid tissue. Note few or no goblet cells, and absence of conventional dysplasia. Lower panel: Dysplastic corrupted crypts in colonic GALT-mucosa. Note highly differentiated carcinoma evolving from dysplastic corrupted crypts in e and f. Hematoxylin and eosin, a, c, d: ×10; b, e, f: ×20.

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    Figure 2.

    Histological features in colon tissue from in dimethylhydrazine-treated Sprague-Dawley rats. Upper panel: Highly differentiated carcinomas in colonic gut-associated lymphoid tissue (GALT) mucosa evolving from dysplastic corrupted crypts in a and b. Detail of highly differentiated carcinoma in c. Lower panel: Signet-ring cell carcinoma in colonic GALT mucosa (d), evolving from dysplastic goblet cells present at the base of crypts in e and f. Hematoxylin and eosin, a: ×10; b, d ×4; c, f ×20; e: ×40.

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Anticancer Research: 37 (3)
Anticancer Research
Vol. 37, Issue 3
March 2017
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The Histogenesis of the Third Pathway of Colonic Carcinogenesis in Rats
CARLOS A. RUBIO
Anticancer Research Mar 2017, 37 (3) 1039-1042;

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The Histogenesis of the Third Pathway of Colonic Carcinogenesis in Rats
CARLOS A. RUBIO
Anticancer Research Mar 2017, 37 (3) 1039-1042;
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Keywords

  • Colon
  • rats
  • Gut-associated lymphoid tissue
  • GALT
  • pathology
  • Dysplasia
  • crypts
  • Carcinoma
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