Unusual presenting manifestation of a rare polyposis, Cowden syndrome

Gastroenterol Hepatol. 2018 May;41(5):315-317. doi: 10.1016/j.gastrohep.2017.06.005. Epub 2017 Jul 15.
[Article in English, Spanish]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adenoma / surgery
  • Adenomatous Polyps / diagnosis*
  • Adenomatous Polyps / genetics
  • Adenomatous Polyps / pathology
  • Adult
  • Colonic Neoplasms / diagnosis*
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / pathology
  • Colonoscopy
  • Diagnosis, Differential
  • Duodenal Neoplasms / diagnosis*
  • Duodenal Neoplasms / genetics
  • Duodenal Neoplasms / pathology
  • Exons / genetics
  • Ganglioneuroma / diagnosis*
  • Ganglioneuroma / genetics
  • Ganglioneuroma / pathology
  • Gastroscopy
  • Hamartoma Syndrome, Multiple / complications
  • Hamartoma Syndrome, Multiple / diagnosis*
  • Hamartoma Syndrome, Multiple / genetics
  • Hamartoma Syndrome, Multiple / pathology
  • Humans
  • Hyperpigmentation / etiology
  • Intestinal Polyps / diagnosis*
  • Intestinal Polyps / genetics
  • Intestinal Polyps / pathology
  • Male
  • Megalencephaly / etiology
  • Multiple Endocrine Neoplasia Type 2a / diagnosis
  • Mutation, Missense
  • PTEN Phosphohydrolase / genetics
  • Penile Diseases / etiology
  • Point Mutation
  • Thyroid Neoplasms / surgery
  • Thyroidectomy

Substances

  • PTEN Phosphohydrolase
  • PTEN protein, human