Výsledky vyhledávání - "HYPERPLASTIC POLYPOSIS"

Akademický článek

Comment on Balsamo et al.: 'Birt–Hogg–Dubé syndrome with simultaneous hyperplastic polyposis of the gastrointestinal tract: case report and review of the literature'

Autor: Flávia Balsamo, Pedro Augusto Soffner Cardoso, Sergio Aparecido do Amaral Junior, Therésè Rachell Theodoro, Flavia de Sousa Gehrke, Maria Aparecida da Silva Pinhal, Bianca Bianco, Jaques Waisberg

Publikováno v: BMC Medical Genomics, Vol 15, Iss 1, Pp 1-4 (2022)

Abstract In this comment, we highlight the diagnosis of Birt–Hogg–Dubé (BHD) in a 60-year-old man was made from identification and removal of normochromic papular cutaneous lesions whose histological examination indicated trichodyscomas and whic

Externí odkaz: https://doaj.org/article/b9fd905eb7ad4dddbec0eab420f916d2

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Akademický článek

Comment on Balsamo et al.: Birt-Hogg-Dubé syndrome with simultaneous hyperplastic polyposis of the gastrointestinal tract: case report and review of the literature

Autor: Irma van de Beek, Maurice A. M. van Steensel, Arjan C. Houweling

Publikováno v: BMC Medical Genomics, Vol 15, Iss 1, Pp 1-4 (2022)

Abstract The publication by Balsamo and colleagues describes a patient with Birt-Hogg-Dubé syndrome and hyperplastic polyposis throughout the gastro-intestinal tract. We question whether the diagnosis of BHD in this patient was justified. Using the

Externí odkaz: https://doaj.org/article/dc465f720f754a25b056be7757f093cc

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Akademický článek

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Akademický článek

Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS)

Autor: Sukanya Horpaopan, Jutta Kirfel, Sophia Peters, Michael Kloth, Robert Hüneburg, Janine Altmüller, Dmitriy Drichel, Margarete Odenthal, Glen Kristiansen, Christian Strassburg, Jacob Nattermann, Per Hoffmann, Peter Nürnberg, Reinhard Büttner, Holger Thiele, Philip Kahl, Isabel Spier, Stefan Aretz

Publikováno v: Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-10 (2017)

Abstract Background Serrated or Hyperplastic Polyposis Syndrome (SPS, HPS) is a yet poorly defined colorectal cancer (CRC) predisposition characterised by the occurrence of multiple and/or large serrated polyps throughout the colon. A serrated polyp-

Externí odkaz: https://doaj.org/article/5480a21676224540bc4fbf489ce2257d

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Serrated polyposis syndrome; epidemiology and management

Autor: S. Carballal, F. Balaguer, J.E.G. IJspeert

Publikováno v: Best practice & research. Clinical gastroenterology.

Serrated colorectal polyps, long considered innocent, are currently recognized as the precursors to one-third of all colorectal cancers (CRC). Serrated polyposis syndrome (SPS), characterized by accumulation of multiple and/or large serrated polyps,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::629c064f16106b3c1f904ddf6c0b143c
http://www.scopus.com/inward/record.url?scp=85126592450&partnerID=8YFLogxK

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Personalised surveillance for serrated polyposis syndrome

Publikováno v: Gut, 69(1), 112-121. BMJ Publishing Group
Gut, 69(1), 112-121. BMJ PUBLISHING GROUP
Gut
Gut, 69, 1, pp. 112-121
Gut, 69, 112-121

Background and aimsSerrated polyposis syndrome (SPS) is associated with an increased risk of colorectal cancer (CRC). International guidelines recommend surveillance intervals of 1–2 years. However, yearly surveillance likely leads to overtreatment

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f400d32493b852e93ecbcb733037ca3
https://doi.org/10.1136/gutjnl-2018-318134

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Akademický článek

Hyperplastic Polyposis Syndrome Identified with a BRAF Mutation

Publikováno v: Gut and Liver, Vol 6, Iss 2, Pp 280-283 (2012)

Background/AimsHydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors (statins) and peroxisome proliferator-activated receptor gamma (PPARγ) ligands can modulate cellular differentiation, proliferation, and apoptosis through various path

Externí odkaz: https://doaj.org/article/74129b5608814602ba29e3e9675e3c66

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Clinical risk factors of colorectal cancer in patients with serrated polyposis syndrome

Autor: Gerrit A. Meijer, Y J van Herwaarden, Evelien Dekker, Susan K. Clark, Joep E. G. IJspeert, N. van Lelyveld, M C W Spaander, Jan J. Koornstra, M E van Leerdam, S A Q Rana, Barbara A. J. Bastiaansen, Tanya M. Bisseling, Iris D. Nagtegaal, Andrew Latchford, James E. East, Nathan S. S. Atkinson, Silvia Sanduleanu

Publikováno v: Gut, 66, 2, pp. 278-284
Gut, 66, 278-284
Gut, 66(2), 278-284. BMJ PUBLISHING GROUP
Gut, 66(2), 278-284. BMJ Publishing Group

Contains fulltext : 169924pub.pdf (Publisher’s version ) (Closed access) OBJECTIVE: Serrated polyposis syndrome (SPS) is accompanied by an increased risk of colorectal cancer (CRC). Patients fulfilling the clinical criteria, as defined by the WHO,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1924ebf2693b1e473877e17772b5536e
https://doi.org/10.1136/gutjnl-2015-310630

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