Psammomatoid Juvenile Ossifying Fibroma Involving Upper Jaw: A Rare Case Report
Published: July 1, 2015 | DOI: https://doi.org/10.7860/JCDR/2015/.6199
Ramlal Gantala, Arjun Yadav Vemula, Jithender Reddy Kubbi, MS Muni Sekhar, Dinesh Jhawar
1. Associate Professor, Department of Oral Medicine and Radiology, SVS Institute of Dental Sciences, Appanapalli, Mahabubnagar, Telangana, India.
2. Post Graduate Student, Department of Oral Medicine and Radiology, SVS Institute of Dental Sciences, Appanapalli, Mahabubnagar, Telangana, India.
3. Reader, Department of Oral Medicine and Radiology,SVS Institute of Dental Sciences, Appanapalli, Mahabubnagar, Telangana, India.
4. Professor and HOD, Department of Oral and Maxillofacial Pathology, SVS Institute of Dental Sciences, Appanapalli, Mahabubnagar, Telangana, India.
5. Associate Professor, Department of Oral and Maxillofacial Surgery, SVS Institute of Dental Sciences, Appanapalli, Mahabubnagar, Telangana, India.
Correspondence
Dr. Arjun Yadav Vemula,
1-1-652/C, Gandhi Nagar, Hyderabad – 500080, Telangana, India.
E-mail : arjunvemula2@gmail.com
Juvenile ossifying fibroma (JOF) is a fibro-osseous neoplasm, rare in occurrence and usually seen in young children. JOF is locally aggressive spreads quickly and is defined as a variant of ossifying fibroma. There are two types of ossifying fibroma depending on histopathology and classified as Psammomatoid juvenile ossifying fibroma (PJOF), Trabecular juvenile ossifying fibroma (TJOF). Both the types affect skull bones with the trabecular type being more common in the jaws- maxillofacial region and the psammomatoid type being more common in the paranasal sinuses, ethmoid sinuses- craniofacial region. Complete excision is mandatory because JOF’s have an extremely high rate of recurrence. A rare case of PJOF involving right maxilla sparing paranasal sinuses in a 15-year-old male patient with clinical, radiographic and histopathological features is discussed.
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