Results 271 to 280 of about 819,681 (335)
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Digestive Endoscopy, 2018
Peutz-Jeghers syndrome is an autosomal dominant disorder with multiple hamartomatous polyps throughout the gastrointestinal tract. The clinical history of patients with Peutz-Jeghers syndrome usually includes multiple laparotomies to treat intestinal ...
T. Yano, S. Shinozaki, H. Yamamoto
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Peutz-Jeghers syndrome is an autosomal dominant disorder with multiple hamartomatous polyps throughout the gastrointestinal tract. The clinical history of patients with Peutz-Jeghers syndrome usually includes multiple laparotomies to treat intestinal ...
T. Yano, S. Shinozaki, H. Yamamoto
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Journal of laparoendoscopic & advanced surgical techniques. Part A, 2018
Background: Conventional high-frequency electrocoagulation (HFEC) of intestinal polyps may be difficult in children and endoscopic mucosal resection (EMR) could be a less invasive option. Chromoendoscopy improves tissue localization during endoscopy, but
Quan Zhan, Chao Jiang
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Background: Conventional high-frequency electrocoagulation (HFEC) of intestinal polyps may be difficult in children and endoscopic mucosal resection (EMR) could be a less invasive option. Chromoendoscopy improves tissue localization during endoscopy, but
Quan Zhan, Chao Jiang
semanticscholar +1 more source
Inflammatory Fibroid Polyps of the Intestine
American Journal of Clinical Pathology, 1984The clinical and pathologic features of 64 inflammatory fibroid polyps of the large and small bowel in 63 patients are reported. Six of the lesions in the small bowel were studied by electron microscopy. Follow-up information was obtained from 39 patients. The lesion was always benign, occurred at all ages, and had a world-wide distribution.
G R, Shimer, E B, Helwig
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The patient with multiple intestinal polyps
Best Practice & Research Clinical Gastroenterology, 2007The management of patients with multiple intestinal polyps may be difficult and greatly depends on the correct classification. Polyposis syndromes account for less than 1% of newly diagnosed colorectal cancers. In addition the risk for extracolonic cancer is increased in most syndromes. Here we report the case of a difficult patient with severe gastric
Karsten, Schulmann +3 more
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The American Journal of Surgery, 1951
Abstract 1. 1. Polyps of the large intestine are frequent. They are usually single but increase in number until in certain patients they become uncountable. 2. 2. Any polyp may develop into carcinoma. The more polyps, the greater tendency for carcinoma to form. 3. 3. All polyps should be removed. 4. 4.
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Abstract 1. 1. Polyps of the large intestine are frequent. They are usually single but increase in number until in certain patients they become uncountable. 2. 2. Any polyp may develop into carcinoma. The more polyps, the greater tendency for carcinoma to form. 3. 3. All polyps should be removed. 4. 4.
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Diagnostic Histopathology, 2011
Abstract Polyps of the small bowel are rare compared to those of the colorectum. A correct histopathological diagnosis is crucial for the choice of subsequent treatment. This article reviews the most frequently found and some rare but distinct polyps and polyp-like lesions in the small intestine.
L.A.A. Brosens +3 more
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Abstract Polyps of the small bowel are rare compared to those of the colorectum. A correct histopathological diagnosis is crucial for the choice of subsequent treatment. This article reviews the most frequently found and some rare but distinct polyps and polyp-like lesions in the small intestine.
L.A.A. Brosens +3 more
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Serrated polyps of the large intestine
Seminars in Diagnostic Pathology, 2005Serrated polyps of the large intestine comprise a family of lesions bearing some histological similarities, including an overall serrated configuration caused at least in part by inhibition of apoptosis by mutations in one of two genes. Over the past decade, it has become apparent that these lesions can be subdivided by histological criteria into ...
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Genetic conditions associated with intestinal juvenile polyps
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2004AbstractJuvenile polyps are hamartomatous polyps found primarily in infants and children, and in association with juvenile polyposis (JP; OMIM# 174900), Cowden syndrome (CS; OMIM# 158350), and Bannayan‐Riley‐Ruvalcaba syndrome (BRRS; OMIM# 153480).
Anders, Merg, James R, Howe
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An Intestinal Polyp of the Umbilical Cord
Archives of Pediatrics & Adolescent Medicine, 1968TUMORS of the umbilical cord are rare. 1,2 It is, therefore, of interest to record the case of a grossly visible, pedunculated polyp of the umbilical cord which, on histological examination, was found to consist of well-formed intestine. Gross Findings A white primigravida, aged 21 years, gave birth at term to a normal male infant weighing 2,949 gm ...
M C, Lee, K, Aterman
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Intestinal lymphangiectasia and colonic polyps: Surgical intervention
Journal of Pediatric Surgery, 1979A 36-mo-old boy with Milroy's Disease, intestinal lymphangiectasia, and an exudative enteropathy (EE), was shown to have four colonic polyps. A large adenomatous polyp was excised from the transverse colon in an effort to control his EE and hypoalbuminemia (1.95 g/dl).
H G, Parsons, P B, Pencharz
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