Infantile myofibromatosis (IM) is a proliferative disorder characterized by
the development of single or multiple nodular lesions arising from cutaneo
us, subcutaneous, muscular, bone or visceral structures. This proliferation
may occur at any anatomical site, but in 30% of the cases it involves the
head and neck. We report here three cases of head and neck IM occurring in
young children and presenting as solitary lesions. The clinical heterogenei
ty and the misleading histopathological appearances can make the diagnosis
difficult. The treatment is surgical but the low rate of recurrence and the
possibility of spontaneous tumoral regression may lead to conservative sur
gery or therapeutic abstention. (C) 1999 Elsevier Science Ireland Ltd. All
rights reserved.