Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report*

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Case Report

Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report*

Ünsal, Özlem, Soytaş, P., Kabukçuoğlu, F., & Uslu Çoşkun, B. (2017). Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report*. ENT Updates, 7(3). https://doi.org/10.2399/jmu.2017003009

Authors

  • Özlem Ünsal

    Clinic of Otorhinolaryngology, Şişli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey
  • Pınar Soytaş

    Clinic of Otorhinolaryngology, Şişli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey
  • Fevziye Kabukçuoğlu

    Clinic of Pathology, Şişli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey
  • Berna Uslu Çoşkun

    Clinic of Otorhinolaryngology, Şişli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey

Juvenile ossifying fibroma is an uncommon, benign, fibro-osseous neoplasm with aggressive local growth. This tumor is distinguished from other fibro-osseous lesions especially by its age of onset, aggressive behavior, and clinical presentation. Two microscopic types have been described: trabecular and psammomatoid variants. In this case report, we presented a young male patient with juvenile psammomatoid ossifying fibroma involving the sinonasal region, skull base and the orbit, which was treated with endoscopic surgery.

Keywords:

Endoscopic sinus surgery juvenile ossifying fibroma psammomatoid variant

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