Surgical management of juvenile nasoangiofibroma extending into adjacent structures: a case report

Authors

  • Adrián A. Izaguirre UMAE Hospital de Especialidades #25, IMSS, Monterrey, Mexico
  • Alejandro A. Sabori Universidad Autónoma de Baja Californ, California, Mexicoia
  • José A. G. Cruz Hospital Universitario General Calixto García, Havana, Cuba
  • Lisset G. H. Torres Hospital General de Zona #3 IMSS Aguascalientes, Jesús María, Mexico
  • Daniel A. Uribe Hospital General de Zona 2-A Francisco del Paso y Troncoso, Mexico City, Mexico
  • Ricardo B. Castañeda C. H. ISSSTE Gómez Palacio, Lerdo, Durango, Mexico
  • Yoselin P. Angeles Universidad Autónoma del Estado de Hidalgo, Pachuca, Mexico
  • Norma G. B. Montaño Universidad de Guadalajara, Hospital Regional Universitario de Colima, Colima, Mexico
  • Juan J. M. Isabeles Hospital General de Subzona y Medicina Familiar N°4, Mexico

DOI:

https://doi.org/10.18203/2349-2902.isj20252292

Keywords:

Juvenile nasoangiofibroma, Endoscopic surgery, Transfacial approach, Skull base, Intraoperative embolization, Maxillectomy, Infratemporal fossa, Skull base surgery, Tumor resection, Multidisciplinary management

Abstract

This case report describes the surgical management of a 16-year-old male diagnosed with a large juvenile nasoangiofibroma extending into the nasal cavity, maxillary sinus, infratemporal fossa, and surrounding structures. The patient presented with a history of progressive facial swelling, nasal obstruction, epistaxis, and left aural fullness. Preoperative imaging, including magnetic resonance imaging (MRI) and angiotomography, demonstrated extensive, highly vascular tumor involvement with critical neurovascular structures. A multidisciplinary surgical approach was employed, combining a Weber-Ferguson transfacial incision with endoscopic sinonasal procedures such as septectomy, turbinectomies, and sphenoidectomy. The operative findings confirmed a large, irregular tumor with attachments to nearby bones and vessels, which was successfully resected with clear margins. Histopathology confirmed juvenile nasoangiofibroma. The postoperative course was favorable, with no complications, and ongoing follow-up was planned to monitor for recurrence. This case highlights the importance of preoperative embolization, tailored surgical strategies, and multidisciplinary collaboration in managing extensive juvenile nasoangiofibromas to achieve optimal outcomes while minimizing morbidity.

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References

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Published

2025-07-28

How to Cite

Izaguirre, A. A., Sabori, A. A., Cruz, J. A. G., Torres, L. G. H., Uribe, D. A., Castañeda, R. B., Angeles, Y. P., Montaño, N. G. B., & Isabeles, J. J. M. (2025). Surgical management of juvenile nasoangiofibroma extending into adjacent structures: a case report . International Surgery Journal, 12(8), 1364–1367. https://doi.org/10.18203/2349-2902.isj20252292

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Section

Case Reports