- Pictorial Review
- Open Access
Multimodality imaging of paragangliomas of the head and neck
© The Author(s). 2019
- Received: 16 July 2018
- Accepted: 14 November 2018
- Published: 4 March 2019
Paragangliomas arise from paraganglion cells which serve varied regulatory tasks in the body. When these cells demonstrate neoplasia within the head and neck, they typically present in characteristic locations including the carotid space, the jugular foramen, the middle ear, and along the course of the vagus nerve. The goal of this article is to review the relevant anatomy related to head and neck paragangliomas, as well as their typical imaging characteristics on cross-sectional imaging including CT, MR, ultrasound, and nuclear medicine studies. Additionally, differential considerations, as well as relevant involvement of adjacent structures which should be conveyed to the clinician, will be discussed.
- Glomus tumor
Paragangliomas arise from paraganglion cells. These cells serve varied regulatory tasks in the body, including chemoreceptor functions, which allow the body to respond to stresses such as hypoxia, hypercapnia, and hypoglycemia.
The imaging evaluation of head and neck paragangliomas utilizes multiple cross-sectional imaging modalities including CT, MR, ultrasound, and various nuclear medicine techniques.
Head and neck paragangliomas most common anatomic locations include the carotid space, jugular foramen, middle ear, and along the course of the vagus nerve.
Paragangliomas are vascular tumors and demonstrate avid enhancement on both CT and MR. They also often exhibit a characteristic “salt and pepper” appearance on MR.
Paragangliomas, also known as glomus tumors, arise from paraganglion cells which form the basis of the extra-adrenal neuroendocrine system. These cells serve varied regulatory tasks in the body, including chemoreceptor functions, which allow the body to respond to stresses such as hypoxia, hypercapnia, and hypoglycemia. When these cells demonstrate neoplasia within the head and neck, they typically present in characteristic locations, and with common symptomatology; thus, understanding these key features in conjunction with their imaging appearance can lead to accurate and prompt diagnosis. The imaging evaluation of head and neck paragangliomas utilizes multiple cross-sectional imaging modalities to evaluate for extent of disease and to help guide surgical management by evaluating for osseous and neurovascular involvement. In this article, we will review the expected anatomic locations of paragangliomas and their general imaging appearance on computed tomography (CT) and magnetic resonance (MR), as well as CT and MR angiography. Additionally, we will discuss other differential considerations for lesions found in these locations. By understanding these fundamental concepts, the radiologist will be able to accurately differentiate a generally benign paraganglioma from a potentially more aggressive head and neck neoplasm.
While the majority of cases are sporadic, approximately 40% are thought to be hereditary . These familial tumors tend to occur earlier than their sporadic counterparts, with a peak prevalence of 30–35 years of age . Additionally, familial paragangliomas are more commonly multicentric than sporadic tumors. Paragangliomas of the head and neck are more common in females, with this predilection most common in jugular (3:1) and tympanic subtypes (6:1) . Paragangliomas are associated with multiple syndromes and genes and are commonly seen in patients with von Hippel-Lindau (VHL), neurofibromatosis type I (NF I), and multiple endocrine neoplasia type II (MEN II) [7, 8].
Magnetic resonance (MR) imaging is the most sensitive imaging modality for evaluation of paragangliomas given its superior soft tissue resolution, and it can readily characterize these tumors from other head and neck neoplasms. Compared to the adjacent soft tissues, paragangliomas typically demonstrate hypointense signal on T1-weighted sequences and isointense to hyperintense signal on T2-weighted sequences. Given the vascular nature of most paragangliomas, internal flow voids are commonly seen, particularly on T2-weighted sequences. More rarely, areas of hyperintense intertumoral hemorrhage can be seen on both T1- and T2-weighted sequences. Interspersing of these, hypointense flow voids and hyperintense areas of hemorrhage results in a characteristic “salt and pepper” appearance which is most apparent in tumors greater than 1 cm. Paragangliomas most commonly demonstrate avid, homogenous enhancement after administration of intravenous gadolinium contrast agents.
On computed tomography (CT), paragangliomas present as a well-defined soft tissue attenuation mass. They most commonly demonstrate homogenous, avid enhancement after administration of intravenous contrast, though heterogeneity can occur in lesions with intratumoral thrombosis or hemorrhage. Additionally, paragangliomas may cause local erosion of adjacent bony structures, and CT imaging is excellent for evaluation of osseous involvement. In the case of paragangliomas involving the skull base, dedicated high-resolution temporal bone CT is typically performed to evaluate the involvement of key structures and to guide surgical management.
Angiography, either with CT angiography (CTA), MR angiography (MRA), or digital subtraction angiography (DSA), is typically performed either as an adjunct to CT or MR, as well as in the preoperative setting . These modalities allow for evaluation of tumor perfusion and identification of feeding vessels, which can guide subsequent embolization or surgical approaches . Given the vascular nature of paragangliomas within the head and neck, angiography typically demonstrates multiple enhancing, feeding peri-tumoral vessels, including arterial and venous vasculature. Additionally, both CTA and MRA are useful for demonstrating the presence of multicentric disease [11, 12].
Carotid body paragangliomas
Carotid body paragangliomas are the most common paragangliomas within the head and neck, accounting for approximately 60% of all cases. The majority of cases occur in older patients, ranging from 40 to 70 years of age with a median age of 57 . As their name suggests, they arise from the carotid body, a grouping of chemoreceptors which reside between the internal and external carotid arteries at the bifurcation of the common carotid artery. The carotid body provides regulatory function for both oxygenation, carbon dioxide, and pH within the blood. Carotid body tumors classically present as slow-growing, painless swelling in the lateral neck , often laterally mobile but fixed vertically (known as Fontaine’s sign). As the tumor grows within the carotid space, it can compress the adjacent nerves (most commonly the vagus nerve), resulting in symptoms such as dysphagia, hoarseness, or Horner’s syndrome . The majority of carotid body paragangliomas are unilateral, though bilateral lesions are seen in approximately 18% of patients . Increased incidence (up to 10% of patients) of sporadic carotid body paragangliomas is seen in patients living at high altitude, or in the setting of chronic obstructive lung disease .
Vagal paragangliomas occur within one of the ganglia of the vagus nerve (CN X). They are the least common head and neck paraganglioma, accounting for approximately 5% of all cases . Vagal paragangliomas are typically seen in middle-aged or elderly patients, with a mean age of 48 years old . Like carotid body tumors, they typically present as a slow-growing, painless neck mass. However, symptomatology differs in that both vagal nerve palsy and hoarseness due to vocal cord paralysis are quite common, seen in 33–37% of patients [6, 21].
Jugular paragangliomas are the second most common head and neck paraganglioma , and the most common tumor found within the jugular fossa. They arise from paraganglia associated with the adventitia of the jugular bulb. The average presentation is 53 years of age; the most common presenting clinical symptoms are unilateral tinnitus or hearing loss (51% of patients) .
Tympanic paragangliomas are the most common tumor of the middle ear . They arise from the tympanic branch of the glossopharyngeal nerve (CN IX), also known as the Jacobsen nerve. The mean age of presentation is 60 years of age, and there is a marked female predilection, with 80–90% of tympanic paragangliomas seen in women [6, 23]. Like jugular paragangliomas, they most commonly present with pulsatile tinnitus or unilateral hearing loss. These tumors are commonly seen as red or blueish, pulsatile masses within the middle ear on otoscopic examination .
Paragangliomas are rare head and neck tumors but are an important differential consideration when a mass is seen in their characteristic locations. They commonly occur within the carotid space, jugular foramen, middle ear, and along the course of the vagus nerve. These vascular tumors demonstrate avid enhancement on CT and MR and often exhibit a characteristic “salt and pepper” appearance. Knowledge of their common locations and characteristic appearance on imaging can allow the radiologist to promptly and accurately diagnose these generally benign lesions. Additionally, by understanding the important imaging findings and associated anatomic involvement of each type of paraganglioma and concisely conveying them to referring clinicians and surgeons, the radiologist can impact subsequent management decisions for the patient.
JT drafted the manuscript. AB participated in its design and editing. All authors contributed cases. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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