5 Facts you should know about

Infantile Myofibromatosis

Infantile Myofibromatosis (IM) is a rare benign soft tissue tumor affecting infants

IM can present as solitary or multifocal lesions involving skin, muscle, bone, and viscera

IM may involve multiple organ systems, requiring a multidisciplinary approach

Some IM cases are associated with genetic mutations, including PDGFRB gene mutations

Prognosis varies, with spontaneous resolution in some cases; treatment includes surgery or medical management

Rare Oncology News