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]
Affiliations
- 1 Servicio de Aparato Digestivo, Hospital Universitario Infanta Leonor, Madrid, España. Electronic address: ladan.hulp@salud.madrid.org.
- 2 Servicio de Aparato Digestivo, Hospital Universitario Infanta Leonor, Madrid, España.
- 3 Servicio de Anatomía Patológica, Hospital Universitario Infanta Leonor, Madrid, España.
No abstract available
MeSH terms
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Adenoma / surgery
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Adenomatous Polyps / diagnosis*
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Adenomatous Polyps / genetics
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Adenomatous Polyps / pathology
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Adult
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Colonic Neoplasms / diagnosis*
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Colonic Neoplasms / genetics
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Colonic Neoplasms / pathology
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Colonoscopy
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Diagnosis, Differential
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Duodenal Neoplasms / diagnosis*
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Duodenal Neoplasms / genetics
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Duodenal Neoplasms / pathology
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Exons / genetics
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Ganglioneuroma / diagnosis*
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Ganglioneuroma / genetics
-
Ganglioneuroma / pathology
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Gastroscopy
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Hamartoma Syndrome, Multiple / complications
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Hamartoma Syndrome, Multiple / diagnosis*
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Hamartoma Syndrome, Multiple / genetics
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Hamartoma Syndrome, Multiple / pathology
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Humans
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Hyperpigmentation / etiology
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Intestinal Polyps / diagnosis*
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Intestinal Polyps / genetics
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Intestinal Polyps / pathology
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Male
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Megalencephaly / etiology
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Multiple Endocrine Neoplasia Type 2a / diagnosis
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Mutation, Missense
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PTEN Phosphohydrolase / genetics
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Penile Diseases / etiology
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Point Mutation
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Thyroid Neoplasms / surgery
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Thyroidectomy
Substances
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PTEN Phosphohydrolase
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PTEN protein, human