Table of Contents

HK J Paediatr (New Series)
Vol 9. No. 2, 2004

HK J Paediatr (New Series) 2004;9:162-166

Case Report

Congenital Infantile Myofibromatosis: A Case Report and Review of Literature

MSC Wong, EYW Kwan


Congenital infantile myofibromatosis is a rare disorder with multiple fibromatous tumours in skin, bone, muscle, viscera and subcutaneous tissue presenting in early infancy. Multiple lytic bone lesions and vertebra involvement are also common, mimicking the clinical picture of metastatic tumours. However, it is a disease with variable prognosis depending on the type and extent of involvement. Spontaneous resolution occurs in most of the cases without visceral involvement. We report good outcome in a case of multicentric type of infantile myofibromatosis with no visceral involvement. Invasive investigations and aggressive intervention should be avoided in these cases.

Keyword : Clinical presentation; Congenital infantile myofibromatosis; Histology; Management; Radiological finding

Abstract in Chinese


This web site is sponsored by Johnson & Johnson (HK) Ltd.
©2022 Hong Kong Journal of Paediatrics. All rights reserved. Developed and maintained by Medcom Ltd.