A case of multiple endocrine neoplasia type 1 with primary liver gastrinoma

J Korean Med Sci. 2010 Jun;25(6):953-6. doi: 10.3346/jkms.2010.25.6.953. Epub 2010 May 25.

Abstract

Gastrinoma is the most frequent functional pancreaticoduodenal endocrine tumor in patients with multiple endocrine neoplasia type 1 (MEN 1). Primary hepatic gastrinomas in MEN 1 are very rare, with no previous reports published in the literature. We reported the case of a 39 yr old female patient with a history of repeated peptic ulcers and a hypoglycemia episode. Abdominal CT indicated a well-defined liver mass and a pancreatic head mass. Somatostatin-receptor scintigraphy with [(111)In] DTPA octreotide demonstrated a strong uptake of the radiotracer in the left lateral segment at the site of the hepatic mass. After operation, immunohistochemical staining was consistent with pancreatic insulinoma and primary hepatic gastrinoma. As the liver is a common site of metastases from gastrinoma, primary liver gastrinoma has not yet been reported with MEN 1. We diagnosed this patient using immunohistochemical studies and treated this patient by hepatic segmentectomy.

Keywords: Gastrinoma; Insulinoma; Multiple Endocrine Neoplasia Type 1.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Gastrinoma / complications
  • Gastrinoma / diagnosis*
  • Gastrinoma / pathology
  • Humans
  • Hypoglycemia / etiology
  • Insulinoma / complications
  • Insulinoma / diagnosis
  • Insulinoma / pathology
  • Liver Neoplasms / complications
  • Liver Neoplasms / diagnosis*
  • Liver Neoplasms / pathology
  • Mastectomy, Segmental
  • Multiple Endocrine Neoplasia Type 1 / complications
  • Multiple Endocrine Neoplasia Type 1 / diagnosis*
  • Pancreatic Neoplasms / complications
  • Pancreatic Neoplasms / diagnosis
  • Pancreatic Neoplasms / pathology
  • Peptic Ulcer / etiology
  • Tomography, X-Ray Computed