| Literature DB >> 26588460 |
Cristina Barrena López1, Alicia Bollar Zabala1, Enrique Úrculo Bareño1.
Abstract
Juvenile psammomatoid ossifying fibroma (JPOF) is a fibroosseous tumor that arises in the craniofacial bones in young people. This lesion usually originates in the jaw, orbit, and ethmoid complex but can also be associated with the skull base and calvaria. Diagnosis must be made based on observing typical radiological and histopathological features. Although JPOF is a rare pathological entity, neurosurgeons must consider this odontogenic lesion in the differential diagnosis of skull masses given the lesion's aggressive behavior and locally invasive growth. Treatment must be gross-total resection. In the following article, the authors present a case of cranial JPOF and discuss various aspects of this entity.Entities:
Keywords: FD = fibrous dysplasia; JOF = juvenile ossifying fibroma; JPOF = juvenile psammomatoid ossifying fibroma; JTOF = juvenile trabecular ossifying fibroma; PEPM = primary extracranial psammomatoid meningioma; juvenile psammomatoid ossifying fibroma; oncology; ossifying fibroma; pediatric skull lesions
Mesh:
Year: 2015 PMID: 26588460 DOI: 10.3171/2015.7.PEDS1521
Source DB: PubMed Journal: J Neurosurg Pediatr ISSN: 1933-0707 Impact factor: 2.375