Multiple adenomatous duodenal polyposis

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F13%3A43907259" target="_blank" >RIV/00216208:11120/13:43907259 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1155/2013/181704" target="_blank" >http://dx.doi.org/10.1155/2013/181704</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1155/2013/181704" target="_blank" >10.1155/2013/181704</a>

Result language
angličtina
Original language name
Multiple adenomatous duodenal polyposis
Original language description
Multiple duodenal polyps are a relatively rare finding, usually co-occurrent with familial adenomatous polyposis (FAP).We report a patient with multiple duodenal adenomas and a negative examination for FAP: multiple flat polyps were detected endoscopically in a 37-year-old male patient, extending from the apex of the bulb to the end of the descending part of the duodenum. In terms of histology, they were tubular adenomas with moderate dysplasia. Colonoscopy and enteroclysis were normal. Both push and capsule enteroscopy only showed multiple polyps in the area of the descending duodenum. DNA analysis of the APC gene was as follows: DGGE, exon 1?15, deletion at codons 1309 and 1061 by means of PCR for attenuated APC were negative. Afterwards we screenedthe patient for germline MYH mutations using the denaturing high-performance liquid chromatography (DHPLC) in combination with sequencing. No novel pathogenic mutation has been identified. Large polyps were removed by means of endoscopic
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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