Skip to main content

Advertisement

Log in

Rectal carcinoid tumor associated with the Peutz-Jeghers syndrome

  • Published:
Journal of Gastroenterology Aims and scope Submit manuscript

Abstract:

A 16-year-old man who had been diagnosed with the Peutz-Jeghers syndrome at the age of 8 years presented with crampy abdominal pain. Thorough examinations revealed a large jejunal polyp causing intussusception, as well as multiple polyps in the small and large intestines. Preoperative proctoscopy demonstrated the coexistence of a submucosal tumor in the rectum. Proctoscopic mucosal resection was performed and histological and immunohistochemical examinations led to a diagnosis of carcinoid tumor. Additional transanal resection of the rectal wall showed no residual tumor and the patient has been well for 2 years to date. Although malignant tumors are increasingly reported in association with the Peutz-Jeghers syndrome, to our knowledge, there have been no previous reports of such an association in the English-language and Japanese literature.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received Jan. 21, 1998; accepted Mar. 27, 1998

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wada, K., Asoh, T., Imamura, T. et al. Rectal carcinoid tumor associated with the Peutz-Jeghers syndrome. J Gastroenterol 33, 743–746 (1998). https://doi.org/10.1007/s005350050166

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s005350050166

Navigation