[Cutaneous myofibroma--late manifestations].

Infantile myofibromatosis is a rare, but nevertheless well-known, entity that was first described in 1954 in Stout's classic article on juvenile fibromatosis. Usually the tumour mass is noted at birth or during the first weeks of life. Solitary lesions are at least twice as common as multiple lesions. A case of a 17-year-old woman with a tumour macroscopically resembling a basal cell epithelioma is presented. This tumour did not develop until the patient was 17 years old and cannot be distinguished histologically from an infantile myofibroma. Because of the very late appearance of this tumour the term "cutaneous myofibroma" is proposed for it. In young patients with a basal cell epithelioma-like lesion the diagnosis of cutaneous myofibroma has to be considered.