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Updated: May 29, 2026

Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development
Published on: July 1, 2020
Spontaneous remission of solitary-type infantile myofibromatosis
Kazuhiro Kikuchi1, Riichiro Abe, Satoru Shinkuma
1Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Tokyo, Japan.
Abstract:
Infantile myofibromatosis is a rare fibrous tumor of infancy. The cutaneous solitary type has typically an excellent prognosis. However, histologically, it is important to rule out leiomyosarcoma, which has a poor prognosis. The low frequency of mitosis was definitive for a diagnosis of infantile myofibromatosis. We present a cutaneous solitary-type case of infantile myofibromatosis. Following incisional biopsy, the tumor remitted spontaneously.
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