Hepatic mesenchymal hamartoma

  • J. B. Yen
  • , M. S. Kong*
  • , J. N. Lin
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

42 Scopus citations

Abstract

Hepatic mesenchymal hamartoma (HMH) is a rare liver tumour in childhood. It is believed to be a benign tumour with a good prognosis if the tumour is excised. Only a few cases with local relapse or metastasis have been reported. We reviewed 134 patients with space-occupying liver lesions, from January 1990 to December 1999, and four patients with HMH were found. Abdominal mass and/or distension were the common initial presentations. Three of our four cases were diagnosed in the first year of life. The liver function tests and tumour markers were non-specific. Case 1 underwent tumour enucleation and another three cases underwent tumour excision. One patient died. No tumour recurrence was noted in the surviving patients.

Original languageEnglish
Pages (from-to)632-634
Number of pages3
JournalJournal of Paediatrics and Child Health
Volume39
Issue number8
DOIs
StatePublished - 11 2003
Externally publishedYes

Keywords

  • Hamartoma
  • Liver
  • Tumour

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