A rare type of polyp in the duodenum.
Peutz–Jeghers syndrome
duodenum
endoscopic resection
polyp
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Oct 2023
Oct 2023
Historique:
received:
12
06
2023
revised:
26
07
2023
accepted:
15
09
2023
medline:
9
10
2023
pubmed:
9
10
2023
entrez:
9
10
2023
Statut:
epublish
Résumé
Although solitary P-J type hamartomatous polyp in the duodenum is rare, the polyp has malignant potential. We should recognize the entity and resect it with a safety margin in case the polyp exhibits an irregular form.
Identifiants
pubmed: 37808567
doi: 10.1002/ccr3.7969
pii: CCR37969
pmc: PMC10551099
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e7969Informations de copyright
© 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
No potential conflict of interest relevant to this article was reported.
Références
J Med Case Rep. 2011 Jun 27;5:240
pubmed: 21707968
Gastroenterol Res Pract. 2019 Sep 08;2019:8159072
pubmed: 31582972