ALLMedicine™ Infantile Myofibromatosis Center
Research & Reviews 47 results
https://doi.org/10.5070/D3271156092
Dermatology Online Journal; Szeto MD, Maymone MB et. al.
Feb 8th, 2022 - Infantile myofibromatosis is a rare myofibroblastic proliferative disorder characterized by firm, skin-colored to red-purple cutaneous and subcutaneous nodules; these are the most prevalent fibrous tumors observed in infancy. A premature male infa...
https://doi.org/10.1002/pbc.29403
Pediatric Blood & Cancer; Sparber-Sauer M, Vokuhl C et. al.
Oct 13th, 2021 - Infantile myofibromatosis (IM) is a rare benign soft tissue tumor and often a self-limiting disease but rarely includes life-threatening complications. Little is known about optimal treatment of primary localized (LD) and multifocal disease (MFD)....
https://doi.org/10.1007/s00381-021-05271-z
Child's Nervous System : ChNS : Official Journal of the I... De Martino L, Tresserras-Giné G et. al.
Jul 11th, 2021 - Infantile myofibromatosis is a rare and nonmalignant pediatric tumor of myofibroblastic origin that may occur in solitary or multifocal forms. Soft tissue of the head and neck, trunk, and extremities, skeleton, and viscera are usually involved. In...
https://emedicine.medscape.com/article/1255879-overview
May 6th, 2021 - Background Solitary fibrous tumor (SFT) was first described in 1870 by Wagner and further established in 1931 by Klemperer and Rabin as a pleural neoplasm. The term hemangiopericytoma (HPC) was first used by Stout and Murray in 1942 to describe a ...
https://emedicine.medscape.com/article/1255879-print
May 6th, 2021 - Background Solitary fibrous tumor (SFT) was first described in 1870 by Wagner and further established in 1931 by Klemperer and Rabin as a pleural neoplasm. The term hemangiopericytoma (HPC) was first used by Stout and Murray in 1942 to describe a ...
