Hepatic mesenchymal hamartoma

Authors


Dr M-S Kong, Department of Pediatrics, Chang Gung Children's Hospital, 6 West, Chia-Pu Road, Putz City, Chiayi, Taiwan, Republic of China. Fax: +886 5 362 3002; email: irishcorners@yahoo.com.tw

Abstract

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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