Exploring a rare case of juvenile psammomatoid ossifying fibroma in the ethmoid: a case study and review

Juvenile ossifying fibroma (JOF) and its variants, including juvenile psammomatoid ossifying fibroma (JPOF), represent rare yet clinically significant benign fibro-osseous lesions that primarily occur in children and young adolescents. They can be found in diverse anatomical sites such as the jaw, n...

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Published in:Journal of surgical case reports Vol. 2024; no. 4; p. rjae242
Main Authors: Aaboudech, Taha Yassine, El Ouazzani, Hafsa, Kadiri, Habiba, Essakalli, Leila, Bouteyine, Ayoub, Benadbdenbi, Hanae, Rguieg, Naji, Cherradi, Nadia
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Published: England Oxford University Press 01-04-2024
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Abstract Juvenile ossifying fibroma (JOF) and its variants, including juvenile psammomatoid ossifying fibroma (JPOF), represent rare yet clinically significant benign fibro-osseous lesions that primarily occur in children and young adolescents. They can be found in diverse anatomical sites such as the jaw, nasal cavity, paranasal sinuses, and orbit. JOF exhibits an aggressive nature, necessitating early radiological detection and surgical intervention. Similarly, JPOF, with a locally malignant potential, requires surgical removal, typically conducted through endoscopic approaches. We report a case of a 5-year-old girl with JPOF arising in the ethmoid, revealed by recurrent epistaxis and proptosis. The text emphasizes the importance of early diagnosis through histopathology as a diagnostic tool and underscores the need for appropriate management.
AbstractList Juvenile ossifying fibroma (JOF) and its variants, including juvenile psammomatoid ossifying fibroma (JPOF), represent rare yet clinically significant benign fibro-osseous lesions that primarily occur in children and young adolescents. They can be found in diverse anatomical sites such as the jaw, nasal cavity, paranasal sinuses, and orbit. JOF exhibits an aggressive nature, necessitating early radiological detection and surgical intervention. Similarly, JPOF, with a locally malignant potential, requires surgical removal, typically conducted through endoscopic approaches. We report a case of a 5-year-old girl with JPOF arising in the ethmoid, revealed by recurrent epistaxis and proptosis. The text emphasizes the importance of early diagnosis through histopathology as a diagnostic tool and underscores the need for appropriate management.
Author Bouteyine, Ayoub
Kadiri, Habiba
El Ouazzani, Hafsa
Rguieg, Naji
Cherradi, Nadia
Essakalli, Leila
Benadbdenbi, Hanae
Aaboudech, Taha Yassine
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Issue 4
Keywords fibro-osseous lesions
ethmoid bone
ossifying fibroma
juvenile psammomatoid ossifying fibroma
Language English
License Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2024.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
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Title Exploring a rare case of juvenile psammomatoid ossifying fibroma in the ethmoid: a case study and review
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