UNUSUALLY AGGRESSIVE MYOFIBROMATOSIS IN A NEONATE
Infantile myofibromatosis is a rare tumor of infancy. It is mesenchymal in origin and involves superficial structures or may be visceral. The lesions have been found in nearly all kinds of tissues, including the orbit, bone, lip, oral cavity, central nervous system, gastrointestinal tract, lungs, my...
Main Authors: | Jitendra Hazarey, Shilpa Hazare, Girish Moghe |
---|---|
Format: | Article |
Language: | English |
Published: |
EL-Med-Pub
2012-04-01
|
Series: | Journal of Neonatal Surgery |
Subjects: | |
Online Access: | http://jneonatalsurg.com/documents/vol-1/pdf/jns-1-29.pdf |
Similar Items
-
Extracalvarial Composite Infantile Myofibromatosis: Case Report and Literature Review
by: Alexander Ivanov, et al.
Published: (2016-06-01) -
Infantile myofibromatosis
by: Margarita Larralde, et al.
Published: (2017-12-01) -
Spinal Canal Involvement in Solitary Infantile Myofibromatosis: Case Report
by: S.N. Gautam, et al.
Published: (2017-08-01) -
The infantile myofibromatosis NOTCH3 L1519P mutation leads to hyperactivated ligand-independent Notch signaling and increased PDGFRB expression
by: Dan Wu, et al.
Published: (2021-02-01) -
Infantile myofibromatosis presenting as a bilobed abdominal and anterior mediastinal mass: Resection via clam-shell incision
by: Abdurrahman Mirza, et al.
Published: (2021-05-01)