Literature DB >> 7213139

[Endoscopic resection of hamartoma of the duodenum].

P Sakai, A A de Ceará, S Ishioka, K Iriya, J J Gama-Rodrigues, J B de Mello.   

Abstract

Duodenal tumors are rare and, Brunner's glands proliferation encompass a small percent. The duodenal hamartoma generally has a polypoid configuration. It can present as two clinical conditions; bleeding and obstruction, even though most of the time it is asymptomatic or presents non specific gastrointestinal symptoms. Another possibility is the association with polypoid lesions of the large bowel, as it happens in Peutz Jeghers and Gardner's syndrome. Malignant transformation is exceedingly rare. Endoscopy has an important role, not only to ensure proper diagnosis, but also as a valuable therapeutic option.

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Year:  1980        PMID: 7213139

Source DB:  PubMed          Journal:  Arq Gastroenterol        ISSN: 0004-2803


  2 in total

Review 1.  [Peutz-Jeghers syndrome. Cases at the Mannheim clinic over 25 years].

Authors:  S Loff; L Wessel; H Wirth; B C Manegold; H Pilcher; K L Waag
Journal:  Langenbecks Arch Chir       Date:  1995

Review 2.  Solitary hamartomatous duodenal polyp; a different entity: report of a case and review of the literature.

Authors:  B Acea Nebril; L Taboada Filgueira; A Parajó Calvo; R Gayoso García; D Gómez Rodríguez; F Sánchez González; C Sogo Manzano
Journal:  Surg Today       Date:  1993       Impact factor: 2.549

  2 in total

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