Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report
Juvenile Ossifying Fibroma (JOF) is a rare, non cancerous overgrowth of bone in the face or jaw. There are two subtypes of JOF: Juvenile Psammomatoid Ossifying Fibroma (JPOF) and Trabecular Juvenile Ossifying Fibroma (JTOF). JPOF shows a modest male predominance (1.2:1), an age range of 3 to 49 year...
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JCDR Research and Publications Private Limited
2024-12-01
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| Series: | Journal of Clinical and Diagnostic Research |
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| Online Access: | https://www.jcdr.net/articles/PDF/20419/73888_CE(Ra1)_F(Sh)_QC(PS_IS)_PF1(VD_OM)_redo_PFA_NC(IS)_PN(IS).pdf |
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| author | Anchal Varshney Manish Bhargava Pratijya Raj Karuna Kumari |
| author_facet | Anchal Varshney Manish Bhargava Pratijya Raj Karuna Kumari |
| author_sort | Anchal Varshney |
| collection | DOAJ |
| description | Juvenile Ossifying Fibroma (JOF) is a rare, non cancerous overgrowth of bone in the face or jaw. There are two subtypes of JOF: Juvenile Psammomatoid Ossifying Fibroma (JPOF) and Trabecular Juvenile Ossifying Fibroma (JTOF). JPOF shows a modest male predominance (1.2:1), an age range of 3 to 49 years, with a mean age of 17.7 years. The majority of instances are associated with the orbital bones and paranasal sinuses. Proptosis is the most typical clinical sign of JPOF. Other features include nasal blockage, headaches, facial oedema, discomfort, recurrent sinusitis, and missing teeth. The lesion is identified under a microscope by a fibroblastic stroma that contains small ossicles resembling psammoma bodies. The preferred first-line treatment for JPOF is total resection due to the disease’s potential for rapid growth and recurrence. Hereby, the authors present a rare case of JPOF ossifying fibroma occurring in the left mandibular molar region of a 50-year-old female who complained of continuous expansion of the lower jaw. Although benign, the potential for recurrence necessitates follow-up and can impact treatment planning. Early diagnosis and intervention are crucial for a favourable outcome. |
| format | Article |
| id | doaj-art-f80c631cb57f4a06b4f4c453d698df2b |
| institution | DOAJ |
| issn | 2249-782X 0973-709X |
| language | English |
| publishDate | 2024-12-01 |
| publisher | JCDR Research and Publications Private Limited |
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| series | Journal of Clinical and Diagnostic Research |
| spelling | doaj-art-f80c631cb57f4a06b4f4c453d698df2b2025-08-20T02:40:04ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2024-12-011812081010.7860/JCDR/2024/73888.20419Juvenile Psammomatoid Ossifying Fibroma: A Rare Case ReportAnchal Varshney0Manish Bhargava1Pratijya Raj2Karuna Kumari3Reader, Department of Oral Pathology, Manav Rachna Dental College, SDS, MRIIRS, Faridabad, Haryana, India.Professor and Head, Department of Oral Pathology, Manav Rachna Dental College, SDS, MRIIRS, Faridabad, Haryana, India.Senior Lecturer, Department of Oral Pathology, Manav Rachna Dental College, SDS, MRIIRS, Faridabad, Haryana, India.Senior Lecturer, Department of Oral Pathology, Manav Rachna Dental College, SDS, MRIIRS, Faridabad, Haryana, India.Juvenile Ossifying Fibroma (JOF) is a rare, non cancerous overgrowth of bone in the face or jaw. There are two subtypes of JOF: Juvenile Psammomatoid Ossifying Fibroma (JPOF) and Trabecular Juvenile Ossifying Fibroma (JTOF). JPOF shows a modest male predominance (1.2:1), an age range of 3 to 49 years, with a mean age of 17.7 years. The majority of instances are associated with the orbital bones and paranasal sinuses. Proptosis is the most typical clinical sign of JPOF. Other features include nasal blockage, headaches, facial oedema, discomfort, recurrent sinusitis, and missing teeth. The lesion is identified under a microscope by a fibroblastic stroma that contains small ossicles resembling psammoma bodies. The preferred first-line treatment for JPOF is total resection due to the disease’s potential for rapid growth and recurrence. Hereby, the authors present a rare case of JPOF ossifying fibroma occurring in the left mandibular molar region of a 50-year-old female who complained of continuous expansion of the lower jaw. Although benign, the potential for recurrence necessitates follow-up and can impact treatment planning. Early diagnosis and intervention are crucial for a favourable outcome.https://www.jcdr.net/articles/PDF/20419/73888_CE(Ra1)_F(Sh)_QC(PS_IS)_PF1(VD_OM)_redo_PFA_NC(IS)_PN(IS).pdfcemento ossifying fibromajuvenile trabecular ossifying fibromaossiclespsammoma bodies |
| spellingShingle | Anchal Varshney Manish Bhargava Pratijya Raj Karuna Kumari Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report Journal of Clinical and Diagnostic Research cemento ossifying fibroma juvenile trabecular ossifying fibroma ossicles psammoma bodies |
| title | Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report |
| title_full | Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report |
| title_fullStr | Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report |
| title_full_unstemmed | Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report |
| title_short | Juvenile Psammomatoid Ossifying Fibroma: A Rare Case Report |
| title_sort | juvenile psammomatoid ossifying fibroma a rare case report |
| topic | cemento ossifying fibroma juvenile trabecular ossifying fibroma ossicles psammoma bodies |
| url | https://www.jcdr.net/articles/PDF/20419/73888_CE(Ra1)_F(Sh)_QC(PS_IS)_PF1(VD_OM)_redo_PFA_NC(IS)_PN(IS).pdf |
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