Results 171 to 180 of about 402,657 (223)

Intestinal Lymphoid Polyposis

American Journal of Clinical Pathology, 1974
A case of familial adenomatous polyposis in association with lymphoid polyposis and incomplete Gardner's syndrome is presented. Immunoglobulins were normal. Examples from the literature are used to show that histologically benign lymphoid intestinal polyposis can accompany lymphomas or leukemias, can precede the appearance of lymphomas or leukemias ...
E B, Shaw, G R, Hennigar
openaire   +2 more sources

Extra-Intestinal Manifestations of Familial Adenomatous Polyposis [PDF]

Annals of Surgical Oncology, 2008
Familial adenomatous polyposis (FAP) is an autosomal dominantly inherited disorder, which results from a germ line mutation in the APC (adenomatous polyposis coli) gene.
Thera P Links, André P van Beek
exaly   +2 more sources

Association between Neuroepithelial Tumor and Multiple Intestinal Polyposis (Turcot's Syndrome): Report of a Case and Critical Analysis of the Literature

Neurosurgery, 1991
We report a case of association of a brain tumor with multiple intestinal polyposis (Turcot's syndrome) and offer a critical analysis of the relevant literature with a view to revising the classification of the syndrome in relation to familial multiple ...
Luciano Mastronardi, Luigi Ferrante, Aldo Fortuna   +2 more
exaly   +2 more sources

Chemoprevention of intestinal adenomatous polyposis by acetyl-11-keto-beta-boswellic acid in APCMin/+ mice

International Journal of Cancer, 2013
Acetyl-11-keto-beta-boswellic acid (AKBA) is a derivative of boswellic acid, which is an active component of the gum resin of Boswellia serrata. AKBA has been used as an adjuvant medication for treatment of inflammatory diseases.
Zu-Hua Gao, Xian-Jun Qu, Huiping Liu
exaly   +2 more sources

Generalized Intestinal Polyposis with Melanosis

Gastroenterology, 1953
Summary The history and findings, clinical, radiological, gastroscopic, sigmoidoscopic, gastric biopsy and rectal biopsy of a patient are given, showing, in a sporadic form the syndrome of generalized polyposis of the stomach, duodenum, colon and rectum, also exhibiting melanin pigmentation of the lips, face, and mouth.
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Familial Intestinal Polyposis

Surgical Clinics of North America, 1955
C E, DUKES, H E, LOCKHART-MUMMERY
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Polyposis of Small Intestine

Gastroenterology, 1954
H L, TSENG, L, BRAUNSTEIN
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FAMILIAL INTESTINAL POLYPOSIS

Australian and New Zealand Journal of Surgery, 1963
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The syndromes of intestinal polyposis

Current Problems in Surgery, 1987
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Intestinal polyposis with oral pigmentation

The American Journal of Surgery, 1958
D F, GUISTO, H E, RAITANO, L G, BRIZZOLARA   +2 more
openaire   +2 more sources