Gastric polyposis: case report and review of the literature
DOI:
https://doi.org/10.11606/issn.1679-9836.v100i1p90-93Keywords:
Gastric polyposis, Peütz-Jeguers syndrome, Gastric hamartomatous polypsAbstract
ound in routine endoscopic examinations. We report a case of gastric polyposis manifested as Peütz-Jeghers Syndrome in a 25 years old female patient, with a history of abdominal pain in the epigastric region 12 days before hospital admission associated to vomits and hematemesis 3 days before admission. The patient underwent upper GI endoscopy, which showed multiple regular polypoid lesions with smooth surface. Computed tomography (CT scan) of the abdomen showed a large, coralliform and vegetative lesion of 16.3 x 10.2 x 5.4 cm. The surgical team chose to perform a total gastrectomy with Roux-en-Y reconstruction. The total surgery time was 150 min, with no further complications. Patient were in good clinical conditions, with no complications and was discharged on the 9th postoperative day. Histopathological study of the surgical specimen evidenced multiple gastric polyps of predominant hamartomatous pattern, with focal adenomatous transformation, free surgical margins, suggesting Peütz-Jeghers syndrome. Our patient did not demonstrate mucocutaneous hyperpigmentation, corroborating the fact that hyperpigmentation is not a “sine qua non” condition for the Peütz-Jeghers syndrome.
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Copyright (c) 2021 Rafael Fernandes Coêlho, Diego Laurentino Lima, Raquel Nogueira Cordeiro Laurentino Lima, João Paulo Ribeiro, Gilberto Lima, Euclides Martins

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