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Review
. 2003 Nov;39(8):632-4.
doi: 10.1046/j.1440-1754.2003.00250.x.

Hepatic mesenchymal hamartoma

J-B Yen  1 , M-S Kong, J-N Lin
Affiliations
Review

Hepatic mesenchymal hamartoma

J-B Yen et al. J Paediatr Child Health. 2003 Nov.

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.

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