1.
Dig Dis Sci
; 69(2): 349-354, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38183558
RESUMO
Solitary hamartomatous polyps with identical pathological features of the typical hamartomas of the Peutz-Jegher syndrome are extremely rare. These solitary lesions lack the associated intestinal polyposis, classic mucocutaneous pigmentation, and family history typifying the Peutz-Jegher syndrome. We describe the case of a 31-year-old woman with a giant solitary gastric hamartoma endoscopically diagnosed and laparoscopically resected.