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. 2009 Aug;4(2):113-7.
doi: 10.3171/2009.4.PEDS08321.

Surgical treatment of juvenile nasopharyngeal angiofibroma with intracranial extension. Clinical article

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Surgical treatment of juvenile nasopharyngeal angiofibroma with intracranial extension. Clinical article

Nevo Margalit et al. J Neurosurg Pediatr. 2009 Aug.

Abstract

Object: The purpose of this study was to describe the surgical treatment and outcomes of patients with intracranial extension of juvenile nasopharyngeal angiofibroma (JNA).

Methods: Twenty-one patients who underwent operations for JNAs between 1994 and 2008 were enrolled in the study. Seven patients (33%) had intracranial tumor extension. The middle cranial fossa and cavernous sinus were involved in 4 patients who underwent operations via the combined infratemporal fossa-midfacial degloving approach. The anterior skull base was involved in 3 patients who underwent the subcranialmidfacial degloving approach.

Results: Complete tumor removal was achieved in all patients. Postoperative complications included 1 case of soft-tissue infection. None of the patients had tumor recurrence after a mean follow-up of 42 months (range 29-85 months). No adjuvant therapy was required in any patient.

Conclusions: Combined approaches can be used effectively for treatment of JNAs with intracranial extension without the need for adjuvant therapy.

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  • Letter to the editor: endoscopy or microscopy?
    Snyderman CH, Gardner PA, Fernandez-Miranda JC. Snyderman CH, et al. J Neurosurg Pediatr. 2012 Mar;9(3):336-7; author reply 337. doi: 10.3171/2011.8.PEDS11337. J Neurosurg Pediatr. 2012. PMID: 22380966 No abstract available.

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