Abstract
In the seminal manuscript by Crohn, Ginsburg, and Oppenheimer in 1932 hemorrhage was not emphasized as a manifestation of “regional enteritis.” The authors noted, however, that “the stools constantly contain occult blood,” and “anemia which ordinarily is moderate may progress to a severe degree” (1). The following year a sequel entitled “Non-specific Granulomata of the intestine” was coauthored by Ginzburg and Oppenheimer (2). In a section on “Hypertrophic Colitis” they described 12 patients with segmentai colonic disease; 5 in the cecum and ascending colon, and 7 in the region of the sigmoid, in whom overt bleeding was a prominent feature. These lesions were characterized by “large irregular ulcerated areas (geographic ulcers), bullous polypoid mucosa, thickened and edematous submucosa, and hypertrophy of serosal fat both in the colon and mesocolon,” all classic features of “Crohn’s disease.”
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Greenstein, A.J., Heimann, T.M. (1999). Intestinal Hemorrhage. In: Michelassi, F., Milsom, J.W. (eds) Operative Strategies in Inflammatory Bowel Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-1396-3_29
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DOI: https://doi.org/10.1007/978-1-4612-1396-3_29
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