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Gastric Adenocarcinoma and Proximal Polyposis of the Stomach in a Hispanic Pediatric Patient With APC Gene Variant c.-191T>G.
Roberts, Annette Gawron; Bujarska, Malgorzata; Bauer, Mislen; Brathwaite, Carole; Pelaez, Liset; Reeves-Garcia, Jesse.
Afiliação
  • Roberts AG; From the Departments of Gastroenterology, Medical Education, and Pathology, Nicklaus Children's Hospital, Miami, Florida.
  • Bujarska M; From the Departments of Gastroenterology, Medical Education, and Pathology, Nicklaus Children's Hospital, Miami, Florida.
  • Bauer M; From the Departments of Gastroenterology, Medical Education, and Pathology, Nicklaus Children's Hospital, Miami, Florida.
  • Brathwaite C; From the Departments of Gastroenterology, Medical Education, and Pathology, Nicklaus Children's Hospital, Miami, Florida.
  • Pelaez L; From the Departments of Gastroenterology, Medical Education, and Pathology, Nicklaus Children's Hospital, Miami, Florida.
  • Reeves-Garcia J; From the Departments of Gastroenterology, Medical Education, and Pathology, Nicklaus Children's Hospital, Miami, Florida.
JPGN Rep ; 2(4): e123, 2021 Nov.
Article em En | MEDLINE | ID: mdl-37206458
Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) is a rare gastric polyposis syndrome defined by numerous polyps (>100) in the fundus and body of the stomach with sparing of the lesser curvature and antrum. GAPPS is linked to a variant in the promoter 1B region of the APC gene. These variants carry a high risk of developing gastric adenocarcinoma, which can occur at an early age. We report a case of GAPPS discovered in a 16-year-old Hispanic girl after endoscopy detected extensive fundic gland polyposis. Genetic testing revealed a promoter 1B point mutation of the APC gene, variant c.-191T>G. Although similar variants have been reported (i.e., c.-191T>C, c.-195A>C, c.-192A>G) in association with GAPPS, variant c.-191T>G has not nor has GAPPS ever been described in a Hispanic individual before.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: JPGN Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: JPGN Rep Ano de publicação: 2021 Tipo de documento: Article