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  • Title: [Infantile myofibromatosis--a case report].
    Author: Eugster AC, Hatt M.
    Journal: Klin Monbl Augenheilkd; 1998 May; 212(5):400-2. PubMed ID: 9677591.
    Abstract:
    A four months old child was referred for a rapidly growing recurrency of a tumor of the left eyebrow. The tumor was excised completely. The pathologic examination revealed an infantile myofibromatosis, most probably of the solitary type. The term "infantile myofibromatosis" summarizes a heterogenous group of rare fibromatoses in childhood, characterized by the proliferation of myofibroblasts. Isolated tumors have a fair prognosis after complete excision.
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