<!DOCTYPE ArticleSet PUBLIC '-//NLM//DTD PubMed 2.8//EN' 'https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd'>
<ArticleSet>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<PubDate PubStatus='aheadofprint'>
				<Year>2026</Year>
				<Month>06</Month>
				<Day>04</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Juvenile nasopharyngeal angiofibroma: nationwide study on incidence, diagnosis, treatment, and recurrence</ArticleTitle>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>El Haddouchi</LastName>
			<Affiliation>Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>P.R.G.</FirstName>
				<LastName>Eriksen</LastName>
			<Affiliation>Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>R.H.</FirstName>
				<LastName>Dahl</LastName>
			<Affiliation>Department of Radiology, Copenhagen University Hospital, Rigshospitalet, Copengagen, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Kongsvad</LastName>
			<Affiliation>Department of Otorhinolaryngology, Odense University Hospital, Odense, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>W.</FirstName>
				<LastName>Krone</LastName>
			<Affiliation>Department of Radiology, Odense University Hospital, Odense, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>G.</FirstName>
				<LastName>Gal</LastName>
			<Affiliation>Department of Radiology, Odense University Hospital, Odense, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Holtmannspoetter</LastName>
			<Affiliation>Department of Neuroradiology, Nuremberg Hospital, Paracelsus Medical University, Nuremberg, Germany</Affiliation>
			</Author>
			<Author>
				<FirstName>G.</FirstName>
				<LastName>Benndorf</LastName>
			<Affiliation>Department of Radiology, Baylor College of Medicine, Houston, TX, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>G.</FirstName>
				<LastName>Lelkaitis</LastName>
			<Affiliation>Department of Pathology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark</Affiliation>
			</Author>
			<Author>
				<FirstName>C.</FirstName>
				<LastName>von Buchwald</LastName>
			<Affiliation>Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark</Affiliation>
			</Author>
		</AuthorList>
<PublicationType>Journal Article</PublicationType>
		<ArticleIdList>
			<ArticleId IdType='pii'>3440</ArticleId>
			<ArticleId IdType='doi'>10.4193/Rhin24.550</ArticleId>
		</ArticleIdList>
		<Abstract>
	    	BACKGROUND: Juvenile nasopharyngeal angiofibroma (JNA) is a rare benign tumour affecting adolescent males, originating near the sphenopalatine foramen and often expanding aggressively. This nationwide study examines the clinical presentation, treat-ment, and prognosis of patients diagnosed from 2003 until mid-2022. METHODS: Patients were identified in the national patho-logy database. The Kaplan-Meier estimator calculated event-free survival, and t-test and Fisher's exact test compared variables. The incidence rates were determined using the 2000 World Health Organization World Standard Population. RESULTS: Sixty-one male patients were included (median age: 16.5 years). The national incidence was 0.12 per 100,000 male person-years (0.43 per 100,000 men at risk (10-24 years)). Common symptoms included nasal obstruction (90%) and epistaxis (59%). Predominant tu-mour stages were Radkowski IIB (31.3%) and Chandler III (65%). Most patients (97%) underwent preoperative embolization, with image-guided endoscopic sinus surgery (ESS) as the primary treatment (86%). Median intraoperative blood loss (IBL) was 500 mL. Radkowski staging correlated with IBL, tumour devascularization, and internal carotid artery (ICA) blood supply. No major compli-cations occurred. Recurrence (25%) was associated with Chandler stage III-IV, with a two-year recurrence-free survival rate of 77%. CONCLUSIONS: Tumour stage correlated with IBL, tumour devascularization, and ICA supply. Recurrence mainly occurred within two years post-surgery, exclusively in advanced-stage cases. With close collaboration between interventionists and rhinologists, preoperative embolization followed by image-guided ESS is recommended as a safe approach with minimal risks.
		</Abstract>
	</Article>
</ArticleSet>