Juvenile Nasopharyngeal Angiofibroma

Juvenile Nasopharyngeal Angiofibroma
Histologic section of a JNA
Identifiers
ICD-9	210.7
ICD-10	D10.6
Outside Resources
Radiopaedia	https://radiopaedia.org/articles/juvenile-nasopharyngeal-angiofibroma?lang=us

Overview

Juvenile nasopharyngeal angiofibroma (JNA) is a benign vascular neoplasm of the nasal cavity and nasopharynx that classically presents in adolescent boys.

Pathophysiology

Relevant Anatomy

JNA's typically originate in the region of the sphenopalatine artery (SPA) in the posterior nasal cavity/nasopharynx. From there, they can extend into the paranasal sinuses, pterygopalatine fossa (PPF), infratemporal fossa (ITF), orbit, or cranial vault.

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  Cadaveric model of the PPF

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  Neural contents of the PPF

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  Maxillary artery branches, with SPA at the distal end

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  Location of the sphenopalatine foramen

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  Location of the ITF

Disease Etiology

JNA's are fibrovascular tumors that arise from the posterior lateral nasal cavity near the choana. There is substantial debate about the exact circumstances and location that lead to the formation of a JNA, but they are generally accepted to form near the region of the sphenopalatine foramen.

Epidemiology

Juvenile nasopharyngeal angiofibroma has been reported to be the most common benign neoplasm of the nasopharynx in young males. It accounts for 0.05% to 0.5% of all head and neck tumors, with a reported incidence of 1 in 5,000 to 1 in 60,000 in the US annually. It classically presents in adolescent males, with a typical age of presentation between 13 and 22 years old.

Genetics

There is no identified definitive genetic locus that predisposes patients to JNA's. However, there have been a number of studies looking at the various genetic components that could influence their formation. Due to fact that JNA's classically form in adolescent males, there have been several studies focused on the possible hormonal influence on their formation and growth. JNA's tend to have an abundance of progesterone and estradiol, but a relatively lower concentration of testosterone and dihydrotestosterone. Supplemental testosterone was trialed in JNA patients, but both tumor growth and tumor recurrence have been documented. Papers investigating potential targeted therapy markers have looked at steroid hormones, chromosomal abnormalities, growth factors, and other intracellular molecular targets. There have been studies investigating a possible link between Familial Adenomatous Polyposis (FAP) and JNA's via the adenomatous polyposis coli (APC)/β-catenin pathway, but no specific genetic link has been identified as of yet.

Diagnosis

Patient History

Patients may have a history of any of the following symptoms:

• Unilateral nasal obstruction
• Recurrent epistaxis
• High-volume epistaxis
• Eustachian tube dysfunction
• Headache
• Facial swelling
• Anosmia / Hyposmia
• Cranial neuropathy
• Vision changes

Physical Examination

Many patients will not have obvious findings on anterior rhinoscopy. A large vascular-appearing mass is commonly fond on nasal endoscopy on the posterior lateral nasal sidewall near the region of the sphenopalatine artery. Note that these hypervascular masses should not be biopsied, as this may result in significant bleeding that is hard to control in the clinic setting.

Laboratory Tests

Laboratory tests are not commonly useful in the diagnosis of JNA's, but should be performed preoperatively in the case of a planned surgical resection.

• Hemoglobin / Hematocrit
• Platelet level
• Platelet function (if family history of platelet dysfunction)
• PT / INR
• Blood Type and Screen (all patients)
• Blood Type and Cross (patients with advanced stage tumors where a significant blood loss is expected)

Imaging

Axial CT scan of a JNA showing a right-sided Holman Miller sign

CT scan, angiography, and MRI are all useful in the workup of JNA's and have differing benefits. CT is typically the first imaging modality ordered in these patients, and is helpful for delineating the extent of bony erosion. Angiography demonstrates the extent of the mass well, and is frequently used in pre-operative embolization 24-48 hours before surgical resection. A majority of JNA's are supplied by the external carotid system, either by the maxillary artery (SPA) or the ascending pharyngeal artery. A lesser fraction of tumors are supplied by the internal carotid system (ophthalmic or sphenoidal branches), and this is typically in larger masses with intracranial invasion. MRI can be used to assess for intraorbital or intracranial extension. JNA's are T1 intermediate, T2 heterogenous with flow voids, and enhance with Gadolinium. The following are general characteristics often found in imaging of JNA's:

• Highly vascular nasopharyngeal mass
• Holman-Miller Sign: Anterior displacement of the posterior maxillary wall due to mass effect from the tumor
• Widening of the PMF or PPF
• Erosion of the pterygoid plate, especially the medial plate

There are several classification systems that have been proposed for JNAs based on imaging findings.

Classification Systems for Juvenile Nasopharyngeal Angiofibromas

Abbreviations: Cavernous sinus (CS), Ethmoid sinus (ES), Infratemporal fossa (ITF), Internal carotid artery (ICA), Maxillary sinus (MS), Nasopharynx (NP), Optic chiasm (OC), Pituitary fossa (PF), Pterygomaxillary fissure (PMF), Pterygopalatine fossa (PPF), Sphenoid sinus (SS)

Classification System	Stage I	Stage II	Stage III	Stage IV	Stage V
Andrews (1989)	Confined to NP	Invading one of the following with evidence of bony erosion: PPF, MS, ES, or SS	Invading ITF or orbit IIIa: No intracranial extension IIIb: Extradural (parasellar) extension	Intradural extension IVa: No infiltration of CS, PF, or OC IVb: Infiltration of CS, PF, or OC	--
Chandler (1984)	Confined to NP	Extension into the nasal cavity, SS, or both	Extension into any of the following: antrum, ES, PMF, ITF, orbit, or cheek	Intracranial extension	--
Onerci (2006)	Nose, NP, ES, and SS or minimal extension into PMF	MS involvement, full occupation of PMF, extension to anterior cranial fossa, limited extension into ITF	Deep extension into cancellous bone at pterygoid base or body and GW of sphenoid, significant lateral extension into ITF or pterygoid plates, orbital involvement, CS obliteration	Intracranial extension between pituitary gland and ICA, tumor localization lateral to ICA, middle fossa extension and extensive intracranial extension	--
Radkowski (1996)	IA: Confined to nose or NP IB: Extends into one or more sinuses	IIa: Minimal extension into medial PMF IIb: Full occupation of PMF with local mass effect IIc: Extension into ITF, cheek, or posterior to pterygoid plates	Erosion of skull base IIIa: Minimal skull base involvement IIIb: Extensive intracranial extension, with or without invasion into CS	--	--
Sessions (1981)	IA: Confined to nose or NP IB: Extends into one or more sinuses	IIa: Minimal extension into PMF IIb: Full occupation of PMF with or without orbital erosion IIc: ITF with or without cheek extension	Intracranial extension	--	--
UPMC (2010)	Nasal cavity, medial PPF	Paranasal sinuses, lateral PPF; no residual vascularity	Skull base erosion, orbit, ITF involvement; no residual vascularity	Skull base erosion, orbit, ITF involvement; residual vascularity	Intracranial extension with residual vascularity M: Medial extension L: Lateral extension

Differential Diagnosis

In the case of a nasopharyngeal mass, the following should also be considered:

• Clival chondroma
• Encephalocele
• Esthesioneuroblastoma
• Inverted papilloma
• Nasal polyp
• Nasopharyngeal carcinoma
• Nasopharyngeal teratoma
• Rhabdomyosarcoma
• Vascular malformation

Management

Medical Management

There is no approved medical treatment for management of juvenile nasopharyngeal angiofibromas. The treatment is primarily surgical. Medical management focuses on optimizing patients before surgery, such as addressing any coagulopathies or addressing underlying anemia.