Focal nodular hyperplasia of the liver associated with portal vein agenesis: a morphological and immunohistochemical study of one case and review of the literature

Adv Clin Path. 1999 Oct;3(4):139-45.

Abstract

Congenital absence of portal vein (CAPV) is a rare malformation. To our knowledge, sixteen cases are reported in western literature. All the cases are associated with other diseases, cardiac malformations (12/17 patients; 16 plus the present case) and hepatic neoplasms being the most frequent observations. We present the case of a girl with a complex malformative syndrome consisting of multicystic kidney dysplasia, CAPV and nodular tumor-like mass of the liver. Angiography showed that the splenic vein and superior mesenteric vein joined to form a common trunk directly entering the inferior vena cava above the liver. A review of the CAPV cases of the literature and the clinical and pathological features of the hepatic lesion, classified as Focal Nodular Hyperplasia (FNH), are extensively discussed.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Abnormalities, Multiple / pathology*
  • Biomarkers, Tumor / metabolism
  • Child
  • Female
  • Focal Nodular Hyperplasia / congenital*
  • Focal Nodular Hyperplasia / metabolism
  • Focal Nodular Hyperplasia / pathology
  • Humans
  • Immunohistochemistry
  • Liver / abnormalities
  • Liver / blood supply*
  • Liver / metabolism
  • Liver / pathology
  • Neoplasm Proteins / metabolism
  • Polycystic Kidney Diseases / congenital
  • Polycystic Kidney Diseases / metabolism
  • Polycystic Kidney Diseases / pathology
  • Portal Vein / abnormalities*
  • Portal Vein / metabolism
  • Syndrome

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins