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Intestinal adenocarcinoma originating from an undiagnosed Meckel's diverticulum.
Principe, Daniel R; Nesper, Peter; Metropulos, Anastasia E; Rubin, Jonathan; Marinov, Marin N.
Afiliação
  • Principe DR; Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
  • Nesper P; Chicago Medical School at Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
  • Metropulos AE; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Rubin J; University of Illinois Metropolitan Group Residency Program, Chicago, IL, USA.
  • Marinov MN; Chicago Medical School at Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
J Surg Case Rep ; 2022(5): rjac128, 2022 May.
Article em En | MEDLINE | ID: mdl-35611002
Meckel's diverticulum is a congenital anomaly leading to the formation of a true diverticulum in the distal small intestine. Though most are asymptomatic and discovered incidentally, Meckel's diverticuli can give rise to a wide range of symptoms. Rarely, this can be a malignancy, most commonly a carcinoid tumor. Other cancers have also been reported, with adenocarcinomas being particularly rare. Here, we report the case of a 62-year-old man presenting to the emergency room with vague gastrointestinal symptoms. Subsequent workup revealed a 3 cm mass in the distal jejunum/proximal ileum, which was located within a previously undiagnosed Meckel's diverticulum. The mass was sent to pathology, who confirmed an adenocarcinoma arising from a small bowel diverticulum. This case serves as an important reminder of the malignant potential of a Meckel's diverticulum and adds to the ongoing discussion regarding whether prophylactic diverticulectomy should be recommended to patients with a known Meckel's diverticulum.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Surg Case Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Surg Case Rep Ano de publicação: 2022 Tipo de documento: Article