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A full stomach.

作者信息

Kager Liesbeth M, Meijer Sybren L, Bastiaansen Barbara A J

机构信息

Department of Gastroenterology, Academisch Medisch Centrum/ Universiteit van Amsterdam, Amsterdam, The Netherlands.

Department of Pathology, Academisch Medisch Centrum/ Universiteit van Amsterdam, Amsterdam, The Netherlands.

出版信息

Gastroenterology. 2014 Nov;147(5):974-6. doi: 10.1053/j.gastro.2014.06.003. Epub 2014 Sep 20.

DOI:10.1053/j.gastro.2014.06.003

PMID:25252015

Abstract

摘要

相似文献

A full stomach.

Gastroenterology. 2014 Nov;147(5):974-6. doi: 10.1053/j.gastro.2014.06.003. Epub 2014 Sep 20.

Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation.

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[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].

Ugeskr Laeger. 2013 Nov 18;175(47A).

[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].

Ugeskr Laeger. 2014 Oct 27;176(44).

Juvenile polyposis syndrome presenting with familial gastric cancer and massive gastric polyposis.

J Clin Oncol. 2012 Sep 1;30(25):e229-32. doi: 10.1200/JCO.2012.41.7949. Epub 2012 Jul 23.

Massive Gastric Juvenile Polyposis: A Clinicopathologic Study Using SMAD4 Immunohistochemistry.

Am J Clin Pathol. 2017 Apr 1;147(4):390. doi: 10.1093/ajcp/aqx015.

Gastric cancer and paraneoplastic dermatomyositis as complications of an unrecognized juvenile polyposis syndrome.

Z Gastroenterol. 2019 Apr;57(4):497-500. doi: 10.1055/a-0855-4404. Epub 2019 Mar 14.

JP-HHT phenotype in Danish patients with SMAD4 mutations.

Clin Genet. 2016 Jul;90(1):55-62. doi: 10.1111/cge.12693. Epub 2015 Dec 21.

[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation].

Ugeskr Laeger. 2014 Oct 27;176(44).

SMAD4 juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia presenting in a middle-aged man as a large fungating gastric mass, polyposis in both upper and lower GI tract and iron deficiency anaemia, with no known family history.

BMJ Case Rep. 2020 Dec 22;13(12):e236855. doi: 10.1136/bcr-2020-236855.

引用本文的文献

Clinical and Molecular Characterization of Splicing Variants in Patients with Juvenile Polyposis Syndrome.

Int J Mol Sci. 2024 Jul 20;25(14):7939. doi: 10.3390/ijms25147939.

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A full stomach.

作者信息

Kager Liesbeth M, Meijer Sybren L, Bastiaansen Barbara A J

机构信息

Department of Gastroenterology, Academisch Medisch Centrum/ Universiteit van Amsterdam, Amsterdam, The Netherlands.

Department of Pathology, Academisch Medisch Centrum/ Universiteit van Amsterdam, Amsterdam, The Netherlands.

出版信息

Gastroenterology. 2014 Nov;147(5):974-6. doi: 10.1053/j.gastro.2014.06.003. Epub 2014 Sep 20.

DOI:10.1053/j.gastro.2014.06.003

PMID:25252015

Abstract

摘要

相似文献

A full stomach.

Gastroenterology. 2014 Nov;147(5):974-6. doi: 10.1053/j.gastro.2014.06.003. Epub 2014 Sep 20.

Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation.

Fam Cancer. 2019 Apr;18(2):165-172. doi: 10.1007/s10689-018-0100-8.

[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].

Ugeskr Laeger. 2013 Nov 18;175(47A).

[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].

Ugeskr Laeger. 2014 Oct 27;176(44).

Juvenile polyposis syndrome presenting with familial gastric cancer and massive gastric polyposis.

J Clin Oncol. 2012 Sep 1;30(25):e229-32. doi: 10.1200/JCO.2012.41.7949. Epub 2012 Jul 23.

Massive Gastric Juvenile Polyposis: A Clinicopathologic Study Using SMAD4 Immunohistochemistry.

Am J Clin Pathol. 2017 Apr 1;147(4):390. doi: 10.1093/ajcp/aqx015.

Gastric cancer and paraneoplastic dermatomyositis as complications of an unrecognized juvenile polyposis syndrome.

Z Gastroenterol. 2019 Apr;57(4):497-500. doi: 10.1055/a-0855-4404. Epub 2019 Mar 14.

JP-HHT phenotype in Danish patients with SMAD4 mutations.

Clin Genet. 2016 Jul;90(1):55-62. doi: 10.1111/cge.12693. Epub 2015 Dec 21.

[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation].

Ugeskr Laeger. 2014 Oct 27;176(44).

BMJ Case Rep. 2020 Dec 22;13(12):e236855. doi: 10.1136/bcr-2020-236855.

引用本文的文献

Clinical and Molecular Characterization of Splicing Variants in Patients with Juvenile Polyposis Syndrome.

Int J Mol Sci. 2024 Jul 20;25(14):7939. doi: 10.3390/ijms25147939.