%0 Journal Article
%T Preliminary Report of a True NasoMaxillary Infantile Fibrosarcoma: Single-Modality Management and 2-Year Follow-Up
%A Naveenkumar Jayakumar
%A Singaravelu Ramesh
%A Veerabahu Rathnaprabhu
%J Archive of "Annals of Maxillofacial Surgery".
%D 2019
%R 10.4103/ams.ams_281_18
%X Infantile fibrosarcoma (IFS) is a malignant tumor, commonly presenting in long bones and seldom encountered after 2 years of age. It is extremely rare in the faciomaxillary region. The condition is often mistaken for teratomas, and histopathology/immunohistochemistry is confirmatory. Treatment involves surgical resection as primary modality. Prognosis is much better compared to the adult variant with even scope for spontaneous regression following ˇ°conservativeˇ± resection. We present a case of IFS of the nasomaxillary complex in a 3-month-old female child. We managed our case with surgical resection, and the patient has remained disease free for over 2 years
%K Fibroblastic tumor
%K hemangioma
%K infantile fibrosarcoma
%K teratoma
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585220/