Aller au contenu principal
Accès ouvert déclaré 2019 article

Cowden syndrome: gastrointestinal manifestations of an infrequent polyposis

1Citations signalées, ce qui n’est pas une note de qualité
2Institutions déclarées
1Pays d’affiliation déclarés

Rattachement africain : uy. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

A 58-year-old man, with a history of total thyroidectomy for papillary carcinoma in 2012, presented with rectal bleeding for the last 4 years, without other digestive symptoms or weigh lost. His physical examination revealed macrocephaly (63-cm circumference), skin with multiple verrucous papules of 1 – 3 mm on the face and dorsum of his hands (which histologically were trichilemmomas), papules in the oral mucosa (hamartomatous papillomas), and a furrowed tongue. The rest of his physical examination and laboratory test results were normal. Colonoscopy showed more than 50 sessile hamartomatous polyps of 2 – 5 mm in the rectum and sigmoid colon. Upper gastrointestinal endoscopy showed flat whitish lesions of 3 – 7 mm in the distal esophagus (acanthosis glycogen). In the stomach, multiple sessile polyps of 3 – 5 mm ([ Fig. 1 ]) were resected and histology revealed these to be hamartomas ([ Fig. 2 ]). In the second portion of the duodenum, a few sessile polyps of 4 – 5 mm were resected (histology revealed normal mucosa). Fig. 1 Endoscopic view showing sessile gastric polyps. Fig. 2 Histology of a resected gastric polyp showing a hamartoma. Small-bowel capsule endoscopy revealed multiple polyps of 1 – 3 mm in the duodenum, proximal jejunum ([ Fig. 3 ]), and distal ileum ([ Video 1 ]). Fig. 3 Small-bowel capsule endoscopy images showing jejunal polyps. Video 1 Small-bowel capsule endoscopy revealed multiple sessile polyps of 1 – 3 mm in the duodenum, proximal jejunum, and distal ileum. Quality: mobile 360 480 720 Download Cowden syndrome is a rare entity related to the PTEN gene. It is characterized by the presence of hamartomatous lesions in any location. The diagnostic criteria (International Cowden Consortium criteria) include major and minor criteria ([ Table 1 ]). Major criteria include: multiple gastrointestinal hamartomas or ganglioneuromas, macrocephaly, macular pigmentation of glans penis, mucocutaneous lesions (trichilemmoma, palmoplantar keratoses, oral mucosal papillomatosis, and cutaneous facial papules), and breast, endometrial, or follicular thyroid cancer. Because of the risk of colorectal cancer, surveillance is recommended, with colonoscopy starting at age 35 or 10 years younger than the age of the index relative. Intervals should be based on the findings, with colonoscopy every 1 – 2 years if multiple polyps or adenomatous polyps are present, or every 3 – 5 years if polyps are sparse or no polyps are found [ 1 ] [ 2 ] [ 3 ] [ 4 ]. Table 1 Diagnostic criteria for Cowden syndrome (International Cowden Consortium criteria updated by the National Comprehensive Cancer Network 2018). Major criteria Minor criteria Breast cancer Endometrial cancer Follicular thyroid cancer Multiple gastrointestinal hamartomas or ganglioneuromas Macrocephaly (58 cm in adult women, 60 cm in adult men) Macular pigmentation of glans penis Mucocutaneous lesions: One biopsy-proven trichilemmoma Multiple palmoplantar keratoses Multifocal or extensive oral mucosal papillomatosis Multiple cutaneous facial papules Autism spectrum disorder Colon cancer ≥ 3 esophageal glycogenic acanthoses Lipoma Intellectual disability (IQ ≤ 75) Papillary or follicular variant of papillary thyroid cancer Thyroid structural lesions (adenoma, nodules, goiter) Renal cell carcinoma Single gastrointestinal hamartoma or ganglioneuroma Testicular lipomatosis Vascular anomalies (including multiple intracranial developmental venous anomalies) Operational diagnosis in an individual (either of the following): Three or more major criteria, but one must include macrocephaly, Lhermitte-Duclos disease, or GI hamartomas Two major and three minor criteria Operational diagnosis in a family where one individual meets the revised clinical diagnostic criteria for PTEN hamartoma tumor syndrome or has a PTEN mutation (one of the following): Any two major criteria with or without minor criteria One major and two minor criteria Three minor criteria Endoscopy_UCTN_Code_CCL_1AC_2AC Endoscopy E-Videos https://eref.thieme.de/e-videos Endoscopy E-Videos is a free access online section, reporting on interesting cases and new techniques in gastroenterological endoscopy. All papers include a high quality video and all contributions are freely accessible online. This section has its own submission website at https://mc.manuscriptcentral.com/e-videos

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.

Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Cowden syndrome: gastrointestinal manifestations of an infrequent polyposis
Date Crossref
16/05/2019
Éditeur
Georg Thieme Verlag KG
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Où se fait cette recherche

  • Universidad de la República de Uruguay pays non établi dans la notice
    Université ou école supérieure
  • Hospital de Clínicas Cátedra de Anatomía Patológica pays non établi dans la notice
    Établissement de santé
  • Clínica de Gastroenterología pays non établi dans la notice
    Établissement de santé

Universidad de la República de Uruguay, Cátedra de Anatomía Patológica — Hospital de Clínicas et Clínica de Gastroenterología.

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

PI3K/AKT/mTOR signaling in cancerToxin Mechanisms and ImmunotoxinsReceptor Mechanisms and Signaling

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.