Research Article

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

Volume: 7 Number: 3 November 28, 2017
  • Özlem Ünsal
  • Pınar Soytaş
  • Fevziye Kabukçuoğlu
  • Berna Uslu Coşkun
EN

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

Abstract

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

References

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Details

Primary Language

English

Subjects

Health Care Administration

Journal Section

Research Article

Authors

Özlem Ünsal This is me

Pınar Soytaş This is me

Fevziye Kabukçuoğlu This is me

Berna Uslu Coşkun This is me

Publication Date

November 28, 2017

Submission Date

May 4, 2017

Acceptance Date

-

Published in Issue

Year 2017 Volume: 7 Number: 3

APA
Ünsal, Ö., Soytaş, P., Kabukçuoğlu, F., & Uslu Coşkun, B. (2017). Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report. ENT Updates, 7(3), 157-160. https://izlik.org/JA74HJ96PU
AMA
1.Ünsal Ö, Soytaş P, Kabukçuoğlu F, Uslu Coşkun B. Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report. ENT Updates. 2017;7(3):157-160. https://izlik.org/JA74HJ96PU
Chicago
Ünsal, Özlem, Pınar Soytaş, Fevziye Kabukçuoğlu, and Berna Uslu Coşkun. 2017. “Juvenile Psammomatoid Ossifying Fibroma With Skull Base and Orbital Wall Invasion: A Rare Case Report”. ENT Updates 7 (3): 157-60. https://izlik.org/JA74HJ96PU.
EndNote
Ünsal Ö, Soytaş P, Kabukçuoğlu F, Uslu Coşkun B (November 1, 2017) Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report. ENT Updates 7 3 157–160.
IEEE
[1]Ö. Ünsal, P. Soytaş, F. Kabukçuoğlu, and B. Uslu Coşkun, “Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report”, ENT Updates, vol. 7, no. 3, pp. 157–160, Nov. 2017, [Online]. Available: https://izlik.org/JA74HJ96PU
ISNAD
Ünsal, Özlem - Soytaş, Pınar - Kabukçuoğlu, Fevziye - Uslu Coşkun, Berna. “Juvenile Psammomatoid Ossifying Fibroma With Skull Base and Orbital Wall Invasion: A Rare Case Report”. ENT Updates 7/3 (November 1, 2017): 157-160. https://izlik.org/JA74HJ96PU.
JAMA
1.Ünsal Ö, Soytaş P, Kabukçuoğlu F, Uslu Coşkun B. Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report. ENT Updates. 2017;7:157–160.
MLA
Ünsal, Özlem, et al. “Juvenile Psammomatoid Ossifying Fibroma With Skull Base and Orbital Wall Invasion: A Rare Case Report”. ENT Updates, vol. 7, no. 3, Nov. 2017, pp. 157-60, https://izlik.org/JA74HJ96PU.
Vancouver
1.Özlem Ünsal, Pınar Soytaş, Fevziye Kabukçuoğlu, Berna Uslu Coşkun. Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report. ENT Updates [Internet]. 2017 Nov. 1;7(3):157-60. Available from: https://izlik.org/JA74HJ96PU