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Successful endoscopic resection of an unusually enlarged and pedunculated type I gastric carcinoid tumour.
Odisho, Tanya; Shi, Dongping; Aburashed, Ahmad.
Afiliação
  • Odisho T; Department of Surgery, Detroit Medical Center, Detroit, Michigan, USA tanya.odisho@gmail.com.
  • Shi D; Department of Pathology, Detroit Medical Center, Detroit, Michigan, USA.
  • Aburashed A; Department of Gastroenterology, Detroit Medical Center, Detroit, Michigan, USA.
BMJ Case Rep ; 14(8)2021 Aug 19.
Article em En | MEDLINE | ID: mdl-34413045
Three distinct gastric carcinoid (GC) tumour types have been described based on differing biological behaviour and prognoses. Type I GC tumours account for the vast majority (70%-80%), are associated with chronic atrophic gastritis and have a low metastatic potential. Type II carcinoid tumours are the least common (5%-10%), are related to Zollinger-Ellison syndrome and occur in relation to multiple neoplasia type I. Sporadic type III tumours (15%-25%) are the most aggressive type, are unrelated to gastrin over secretion and carry the worst prognosis. In this case report, we present a patient with longstanding gastroesophageal reflux disease (GERD) who presented with epigastric abdominal pain and tarry stools and was found to have a large gastric polyp on endoscopy. Despite current literature recommending surgical resection for larger GC tumours, endoscopic resection was successfully used to excise the tumour with pathology demonstrating complete resection with negative margins.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Tumor Carcinoide / Síndrome de Zollinger-Ellison / Gastrite Atrófica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: BMJ Case Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Tumor Carcinoide / Síndrome de Zollinger-Ellison / Gastrite Atrófica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: BMJ Case Rep Ano de publicação: 2021 Tipo de documento: Article