Pediatric Endoscopic Skull Base Surgery: Safety, Efficacy, and Lessons Learned. [PDF]
Lander DP +5 more
europepmc +1 more source
A Rare Presentation of Cemento-ossifying Fibroma with Inherent High Flow Vascular Malformation: A Wolf in Sheep's Clothing. [PDF]
Ali M, Mahajan A, Bansal V, Singh AK.
europepmc +1 more source
Juvenile trabecular ossifying fibroma of the sphenoid sinus causing acute visual loss in a 14-year-old girl with Turner syndrome: a case report. [PDF]
Murase E +5 more
europepmc +1 more source
Misdiagnosed long-standing unilateral nasal obstruction: ossifying fibroma of the inferior turbinate. [PDF]
Thomas AS +3 more
europepmc +1 more source
Haberland Syndrome Associated with Juvenile Ossifying Fibroma and Odontoma: Rare Case Report. [PDF]
Alagarsamy R +5 more
europepmc +1 more source
Abstracts from the 34th Portuguese Dental Association Annual Meeting. [PDF]
europepmc +1 more source
Psammomatoid Juvenile Cemento-Ossifying Fibroma of the Maxilla
Both the trabecular and the psammomatoid juvenile cemento-ossifying fibromas (COFs) are specific entities among the COFs being distinguished because of their age predilection, site involvement, and clinical behavior. A case of a large-size juvenile COF of histologic psammomatoid pattern is shown.
Yang, HY +5 more
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Juvenile Psammomatoid Ossifying Fibroma: A Review
Oral Oncology, 2011In WHO classification of odontogenic tumors (2005), juvenile ossifying fibroma (JOF) is divided into juvenile psammomatoid ossifying fibroma (JPOF) and juvenile trabecular ossifying fibroma (JTOF). JPOF has been distinguished because of its location, clinical behavior, and age of occurrence. It is generally seen in younger age group and the most common
Pushkar Waknis, Gargi S. Sarode
exaly +3 more sources
Juvenile psammomatoid ossifying fibroma of the neurocranium
✓ Juvenile psammomatoid ossifying fibroma (JPOF) is a benign fibroosseous lesion predominantly arising within the paranasal sinuses in children and young adults. Neurocranial occurrence is exceedingly rare and a location within the neurocranial portion of the temporal bone has not been described.
Martin, Hasselblatt +7 more
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JUVENILE PSAMMOMATOID OSSIFYING FIBROMA: A CASE REPORT
We herein report a case of a 9-year-old girl with a rare aggressive juvenile psammomatoid ossifying fibroma (JPOF) which also presented with relapsed Wilms’ tumour.
Emilly Silva +3 more
openaire +2 more sources

