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Non-neoplastic pathology at the crossroads between neck imaging and cardiothoracic imaging
Insights into Imaging volume 10, Article number: 116 (2019)
The thoracic inlet is located at the crossroads between imaging of the neck and chest. It represents an important anatomic landmark, serving as the central conducting pathway for many vital structures extending from the neck into the chest and vice versa. Many important body systems are located within this region, including the enteric, respiratory, vascular, lymphatic, neurologic, and endocrine systems. A detailed examination of this region is essential when reviewing neck and thoracic imaging. This article will discuss the normal anatomic boundaries of the thoracic inlet and present an image-rich systematic discussion of the non-neoplastic pathology that can occur in this region. The neoplastic pathology of the thoracic inlet will be covered in a companion article.
The thoracic inlet is an important anatomic region from which various non-neoplastic pathologies can arise.
It contains many vital body systems such as the enteric, respiratory, lymphatic, neurologic, musculoskeletal, and endocrine structures/systems, allowing for the development of a systematic approach to the review of the thoracic inlet.
Many of these findings can be subtle and easily overlooked as the thoracic inlet is located at the crossroad between different imaging specialties.
The thoracic inlet is at the crossroads of imaging, often captured as the first or last set of images obtained during cross-sectional studies of the chest or neck respectively. This ultimately increases the chance this region is overlooked during the interpretation of the study, especially if both regions are imaged, as the neck radiologist may feel that it is part of the chest territory and the chest radiologist may feel that it is part of the neck territory. In addition, confident interpretation of this region can be difficult as many radiologists are fellowship trained in either neuroradiology or cardiothoracic imaging, but not both specialties.
When evaluating the thoracic inlet, it is important to tackle this region with a methodical plan in order to reduce the chance of missing clinically important findings. We propose a systematic approach to the imaging of the thoracic inlet based on the modified form of the classic medical school mnemonic “VINDICATE”, referring to the potential diagnostic etiologies that can be used to create a differential diagnosis (Table 1). The etiologies to consider in this region are vascular, infectious/inflammatory, neurologic (instead of neoplastic which will be covered in a separate article), degenerative, iatrogenic, congenital, autoimmune, traumatic, and endocrine etiologies. This article will discuss the normal anatomic boundaries of the thoracic inlet and present an image-rich systematic discussion of some of the non-neoplastic pathology that can occur in this region based on the mnemonic “VINDICATE”, using different imaging modalities, including plain film, computed tomography (CT), magnetic resonance (MR), and ultrasound (US) imaging. The neoplastic pathology of the thoracic inlet will be covered in a companion article.
Multiple imaging modalities can be utilized to assess the thoracic inlet, including radiography, fluoroscopy, CT, MRI, and ultrasound. In general, radiography is limited in providing spatial details, however is an important screening tool in a trauma setting. Pneumomediastinum and subcutaneous emphysema are well detected by radiographs, as well as osseous abnormalities including conditions such as cervical osteophytes and diffuse idiopathic skeletal hyperostosis (DISH). Fluoroscopy is the workhorse in dynamic visualization of the esophagus. It is a helpful screening tool for esophageal abnormalities such as diverticula, ulcers, stenosis, dysmotility, and cancer. CT provides extensive spatial resolution and is the “gold standard” for evaluating most vascular pathology, cancer staging, and as a quick evaluation tool in the setting of trauma. Evaluation of superficial structures such as the thyroid gland, cervical lymph nodes, and cervical vascular structures can be easily performed with ultrasound, which has the added benefit of portability and lack of radiation exposure. MRI is an advanced modality, with superior soft tissue resolution, critical in the assessment of neural and lymphatic structures such as the brachial plexus and thoracic duct, which cannot be as reliably assessed with CT.
Anatomy of the thoracic inlet
The thoracic inlet is an important anatomic landmark as it contains multiple vital organ structures including the digestive tract, respiratory, vascular, lymphatic, endocrine, and neural structures. The boundaries of the thoracic inlet, however, are best defined by its surrounding osseous structures. The body of the first thoracic vertebrae makes up the posterior and superior margin of the thoracic inlet. The first pair of ribs and their costal cartilages define its lateral margins. Anteriorly and inferiorly, the thoracic inlet is bounded by the superior border of the manubrium. The inlet slopes anteroinferiorly following the first pair of ribs and spans roughly the first through third thoracic vertebral levels (Fig. 1) [1, 2].
Above the level of the first rib, familiarity with the cervical fasciae and infrahyoid neck spaces can help a radiologist construct a comprehensive differential diagnosis of pathology involving the thoracic inlet. The cervical fasciae define the spaces of the neck from which specific diseases can arise. They form important barriers which can limit the spread of infection and certain tumors .
Traditionally, there are two major cervical fasciae, the superficial cervical fascia (SCF) and the deep cervical fascia (DCF). The SCF is a layer of fatty loose connective tissue that covers the head, face, and neck. Its primary function is to allow the skin to glide easily over the deeper structures of the neck. Infections that track along the SCF are superficial and rarely track deeper into the neck. The DCF is made up of denser layers which extend from the skull base inferiorly. There are three layers of the DCF: (1) the superficial layer of the deep cervical fascia (SLDCF) surrounds all the important neck structures; (2) the middle layer of the deep cervical fascia (MLDCF) includes the pretracheal and visceral layers which surround the aerodigestive tract; and (3) the deep layer of the deep cervical fascia (DLDCF) surrounds the vertebral column and paravertebral muscles. The three layers of the DCF delineate the infrahyoid neck spaces, from which we subdivide neck diseases. Figure 2 illustrates the anatomical contents of the infrahyoid neck spaces .
Below the level of the first rib, familiarity with the structures of the upper thorax will play an important role in completing the differential diagnosis for the pathology of the thoracic inlet. The major structures of the upper thorax include the lungs, pleura/pleural space, mediastinum, vascular structures, and the chest wall. The mediastinum contains the esophagus, the trachea, the thymus, the lymph nodes, the thoracic duct, and multiple nerves including the phrenic nerve and the sympathetic chain. Figure 3 illustrates the anatomical contents of the upper thorax.
Given the complex anatomy at the junction of the neck and thorax, an algorithmic approach should be used to determine which region of the thoracic inlet is affected (Fig. 4). Once the area of involvement is identified, applying the VINDICATE pneumonic to the region will help to expand the differential diagnosis to include a comprehensive list of possible causative etiologies.
Normal blood vessels in anomalous location and configuration can mimic a mass and be challenging to interpret. Familiarity with the more common vascular anomalies can increase confidence in interpretation. Alternatively, pathology involving the vasculature in the thoracic inlet can be easily overlooked.
Aberrant right subclavian artery
Aberrant right subclavian artery is a developmental anomaly that is present in approximately 0.5–2% of the population and is the most common congenital anomaly of the aortic arch. It is caused by involution of the embryonic right 4th aortic arch between the left common carotid artery and left subclavian artery. Most patients are asymptomatic; however, symptoms may arise due to mass effect on the posterior esophagus causing dysphagia lusoria, and dyspnea and cough from posterior tracheal compression . Radiography may demonstrate an ill-defined opacity in the right medial clavicular area located posterior to the trachea in the Raider triangle. An esophagram in the lateral view will show an oblique posterior impression on the esophagus. Both CT and MR can be easily used to demonstrate a right subclavian artery branch arising distal to the left subclavian artery origin from the aortic arch and coursing posterior to the trachea and esophagus (Fig. 5).
Partial anomalous pulmonary venous return
Partial anomalous pulmonary venous return is a congenital anomaly in which the pulmonary vein drains into the systemic veins rather than into the left atrium (Fig. 6). Of the various types of partial anomalous pulmonary venous return (PAPVR), imaging at the level of the thoracic inlet may reveal abnormalities of the superior pulmonary veins. Symptoms, if present, typically are related to the left to right shunt and include dyspnea, palpitations, chest pain, tachycardia, edema, and systolic murmur. Right-sided PAPVR typically drains via the superior vena cava (SVC), and left-sided PAPVR typically drains via the left brachiocephalic vein. There may also be an associated sinus venosus atrial septal defect, more commonly present in the setting of a right PAPVR. MR imaging is equivalent to CT for morphologic characterization of PAPVR .
Internal jugular vein thrombus
Thrombosis of the internal jugular vein (IJV) arises from three main mechanisms: (1) endothelial damage from indwelling line or infection, which causes altered blood flow and hypercoagulable state; (2) venous stasis from compression of the neck (including internal jugular vein) or by compression of the mediastinal structures such as the SVC; and (3) malignancy as a risk factor for hypercoagulability. Trousseau syndrome refers to thromboembolism associated with malignancy, and many cancers such as pancreatic, lung, and ovarian cancers have been linked to this phenomenon . Patients typically present with a swollen, hot, tender neck mass and fever in the acute phase (> 10 days) and a palpable tender cord in the neck in the chronic phase. Acute thrombus on CT imaging appears as a non-enhancing filling defect within a distended vein (Fig. 7). Occasionally, however, acute thrombus is hyperdense, best seen on noncontrast imaging, and can potentially mimic a patent IJV on venous (60–90 s delayed) phase of imaging; enlargement of the vein with circumferential fat stranding with adjacent edema in the retropharyngeal space can be clues to the diagnosis. A chronic thrombus typically appears as a well-marginated filling defect; linear stranding and calcifications may be present. The vessel size may be normal or small, and the associated adjacent soft tissue inflammatory changes have typically resolved. Collateral veins may be present. On ultrasound, the clot appears as a solid mass with intermediate echoes and the vein is non-compressible with absent flow on Doppler when the clot is occlusive (Fig. 8) .
Infection of the thoracic inlet region may arise spontaneously, as a result of traumatic injury, surgical complication, or extension from another space such as osteomyelitis or diskitis.
Lemierre’s syndrome is a rare entity characterized by thrombophlebitis of the jugular veins secondary to upper aerodigestive tract infection, with or without peritonsillar or retropharyngeal abscess, otherwise known as post-pharyngitis venous thrombosis. It typically occurs in young adults and is caused by Fusobacterium necrophorum infection of the oropharynx in 80% of patients . Patients present with ipsilateral tonsillar fullness and pain. The classic triad of finding includes neck vein thrombosis and cavitary pulmonary nodules in the setting of pharyngitis. CT imaging typically shows increased tonsil size, possible abscess, ipsilateral vein thrombosis (usually IJV), inflammatory changes of the neck and soft tissue edema, and metastatic seeding of infection (cavitary pulmonary nodules with the appearance of septic emboli, septic joints)  (Fig. 9).
Mediastinitis refers to the nonmalignant proliferation of fibrous tissue and acellular collagen in the mediastinum and is usually caused by an aggressive infectious or inflammatory process. While many cases of chronic mediastinitis are idiopathic, about 90% of cases of acute mediastinitis are secondary to esophageal perforation or rupture. Median sternotomy and radiation therapy are other important iatrogenic etiologies to consider. Patients may present with fever, chills, and/or retrosternal pain. While it can affect any age, it is more common in young adults and can have 25–50% mortality [9, 10]. Radiographs show mediastinal widening, mediastinal air-fluid levels, and pneumomediastinum. CT findings may include diffuse fat stranding of the mediastinum, as well as organized fluid collections in the setting of esophageal perforation (Fig. 10). A clue to localizing the site of esophageal perforation is to look for extraluminal air which will typically be near the area of perforation. It is important to note that the findings in the post-surgical mediastinum can have a similar appearance to mediastinitis in the first 2–3 weeks. Esophagram with water-soluble contrast is recommended in patients with suspected esophageal perforation to better define the area of leak.
The spectrum and symptoms from neurologic pathology of the thoracic inlet can be highly variable as many important nerves traverse this region, including the brachial plexus, vagus nerve, recurrent laryngeal nerves, phrenic nerve, and sympathetic chain. Some examples of non-neoplastic pathology are nerve sheath cysts, laryngeal nerve injury, brachial plexopathy, and post-radiation injury.
Traction injury to the brachial plexus
In adults, brachial plexus avulsion or traction injury to the brachial plexus is typically related to high-energy trauma. In neonates, it is commonly due to excessive traction on the plexus by forceps during difficult delivery. Patients typically present with flail arm or incomplete paralysis. Diagnosis of brachial plexopathy is difficult on CT imaging; however, close evaluation may reveal pseudomeningocele or paraspinal hematoma . MRI is the gold standard for diagnosing brachial plexopathy, typically demonstrating enlarged, hypo- to isointense neural elements on T1-weighted imaging (T1WI) and hyperintense on T2-weighted imaging (T2WI) due to stretch injury (Fig. 11). When there is an avulsion of a brachial plexus nerve root, a pseudomeningocele forms characterized by CSF hyperintensity within an empty root dilated root sleeve. Fat-saturated images are helpful in confirming edema and denervation changes, particularly of the cervical paraspinal muscles . Myelogram may demonstrate a cerebral spinal fluid (CSF) leak and/or pseudomeningocele.
Perineural cyst of the brachial plexus
Perineural cysts, also known as Tarlov cysts, are benign, typically asymptomatic, cerebrospinal fluid filled cystic cavities in the perineural recesses along the dorsal spinal nerve roots . They are most often found along the sacral spine, however can also occur along the brachial plexus. Symptoms arise when a perineural cyst compresses a nerve root, presenting with symptoms of brachial plexopathy or radiculopathy, and these cysts are an important consideration as a possible etiology for brachial plexopathy when imaging exams are otherwise negative . Perineural cysts are best seen on MR imaging and will be low signal on T1WI and high signal on T2WI (Fig. 12).
Degeneration is a gradual deterioration of specific tissues, cells, or organs with impairment or loss of function due to injury, disease, or aging. This process occurs in all organ systems and in the thoracic inlet; this condition is most evident in the musculoskeletal, vascular, and digestive systems.
Esophageal diverticula are saccular protrusions or outpouchings of the esophagus, classified according to their direction of protrusion and location. Zenker’s diverticula extend inferiorly behind the esophagus, just proximal to the upper esophageal sphincter (Fig. 13). Killian-Jamieson diverticula, conversely, are anterolateral protrusions into the Killian-Jamieson space, area of weakness just below the cricopharyngeal muscle (Fig. 14) . These outpouchings can be unilateral or bilateral and are typically smaller than Zenker’s diverticulum, ranging from 3 to 20 mm. In both cases, patients typically present with dysphagia, regurgitation, and aspiration of undigested food, halitosis, hoarseness, and neck mass . Imaging can demonstrate an air-fluid level or contrast-filled outpouching in the thoracic inlet .
Tracheal diverticula can be congenital or acquired, with the congenital variant being less common. Congenital diverticula are often asymptomatic and incidentally detected unless associated with other conditions such as recurrent tracheobronchial infection. The distinction between the two entities is made pathologically, with the congenital tracheal diverticula composed of respiratory epithelium, smooth muscles, and cartilage, and the acquired tracheal diverticula are formed from respiratory epithelium only and lack smooth muscle and cartilage . They both are characterized by single or multiple outpouchings of the tracheal wall, most commonly arising along the right lateral aspect of the trachea where the cartilage rings are deficient and there is no esophagus to support the adjacent tissue (Fig. 15). Most cases are asymptomatic and do not require treatment; however, these structures have the potential to become infected and form an abscess.
Osteophytes are thorn-like or claw-like projections from the margins of vertebral endplates and are typically associated with spondylotic degenerative changes, findings which can be clearly seen on plain film and CT imaging (Fig. 16). Large cervical osteophytes can project anteriorly within the thoracic inlet and cause symptoms of dysphagia; therefore, it is an important imaging finding to include in reports when performing esophograms for dysphagia.
Diffuse idiopathic skeletal hyperostosis
Diffuse idiopathic skeletal hyperostosis (DISH) is a distinct entity from cervical osteophytosis, is of unknown etiology, and causes flowing anterior vertebral ossification. Primary diagnostic criteria include flowing anterior ossification extending over at least four contiguous vertebral bodies, no sacroiliac or apophyseal ankylosis, mild degenerative disc changes, and no facet ankyloses (Fig. 17). DISH can coexist with spondylosis, however complicating the diagnosis. DISH may cause dysphagia due to a combination of mechanical compression and inflammation/fibrosis of the esophageal wall. Associated adjacent ligament ossification around the cervical spine may also result in pain and/or dysphagia. Complications may include decreased mobility due to anterior longitudinal ligament fracture following minor trauma in long column fusion and osteoporosis . CT imaging can confirm the location of ossification, as well as subtle transverse fractures of the anterior longitudinal ligament following minor trauma (Fig. 17). On MR imaging, flowing anterior longitudinal ligament ossification is hypointense on T1W1 and T2WI, unless there is substantial fatty marrow content, in which case they may be hyperintense .
Iatrogenic complications are a broad category of conditions that directly result from healthcare treatment or intervention. Common causes at the level of the thoracic inlet include complications following surgical procedures and post-radiation changes leading to fibrosis and scarring of the region.
While tracheoesophageal fistula (TEF) is almost always congenital in the pediatric population, in adults, it can occur iatrogenically as a complication of malignancy, malignancy treatment, or surgical intervention (Fig. 18). Other less common causes of TEF include sequelae of infection and inflammation as can occur in post-foreign body impaction. Symptoms include excessive oral secretions, cyanosis, choking, and coughing. Fluoroscopic imaging is often the best imaging modality for diagnosis allowing for a real time and dynamic look of the esophageal lumen and may identify the site of communication. Unfortunately, CT and MR imaging often do not visualize the defect if the esophagus is collapsed. Administering oral contrast immediately before CT imaging can improve the detection of the fistulous track connecting the esophagus to the trachea. CT imaging can also be used to evaluate for complications of TEF including evidence of aspiration within the lung parenchyma.
Some frequently encountered congenital anomalies of the thoracic inlet are tracheobronchomegaly, dilated thoracic duct, branchial cleft cysts, narrowed thoracic inlet, and fibromatosis colli, as well as the previously discussed tracheoesophageal fistula and vascular anomalies including the aberrant right subclavian artery and partial anomalous pulmonary venous return.
Tracheobronchomegaly, also known as Mounier-Kuhn syndrome, can be either congenital or acquired. In congenital patients, this condition develops secondary to an underlying abnormality involving the connective tissues, such as Ehlers-Danlos syndrome or cutis laxa, causing atrophy of the tracheal and mainstem bronchial elastic tissue and smooth muscle leading to significant central airway dilatation . Patients typically present with cough and dyspnea, which may mimic or coexist with chronic obstructive pulmonary disease. Radiographs may demonstrate marked dilatation of the trachea and central bronchi. On CT imaging, the condition should be suspected if the trachea, right main bronchus, and left main bronchus measure greater than 3 cm, 2.0–2.4 cm, and 1.5–2.3 cm respectively, with the trachea measurement commonly performed approximately 2 cm above the level of the aortic arch  (Fig. 19). Other CT findings may include posterior tracheobronchial diverticulosis, bronchiectasis, and tracheobronchial collapse with expiration imaging.
Dilated thoracic duct
The thoracic duct drains lymph from the lower extremities, abdomen, and left chest. This structure crosses the thoracic inlet posterior to the left subclavian artery, anterior to the anterior scalene muscle/phrenic nerve, and empties into the venous system at the confluence of the left subclavian and left internal jugular veins in the carotid space . The thoracic duct may be identified in about 55% of cases on routine neck CT imaging . The average diameter of a thoracic duct is 4.8 mm . This structure, however, may enlarge after a large fatty meal, and dilatation of the structure should be considered a normal anatomic variant and considered an incidental finding if seen on imaging. CT imaging will show a left-sided non-enhancing tubular structure which drains into the confluence of the left subclavian and left internal jugular veins  (Fig. 20). On MR imaging, the thoracic duct has hyperintensity on T2-weighted imaging, similar to cerebral spinal fluid (CSF) [1, 19].
Autoimmune conditions are generally systemic, with some demonstrating propensity for specific organs, including those traversing the thoracic inlet. For example, systemic sclerosis can affect the esophagus causing esophageal dilatation . Autoimmune thyroiditis such as Hashimoto’s thyroiditis causes thyroid enlargement with nodules and can have an association with lymphoma . Antiphospholipid syndrome is associated with venous and arterial thrombosis .
Hashimoto’s thyroiditis, also known as chronic autoimmune thyroiditis or chronic lymphocytic thyroiditis, is the most common cause of thyroiditis and hypothyroidism. Patients typically present with gradual painless enlargement of the thyroid gland and symptoms related to hypothyroidism. Grayscale ultrasound tends to vary with different stages of the disease and extent of involvement. The thyroid is typically enlarged with heterogeneous echotexture. Multiple, discrete hypoechoic micronodules from 1 to 6 mm in diameter are strongly suggestive of chronic thyroiditis (Fig. 21). On color Doppler, the thyroid may demonstrate normal or decreased blood flow in later stages; however, it may occasionally be hypervascular, reflecting early phase of the disease and hypertrophic action of thyroid-stimulating hormone (Fig. 21). CT shows symmetric enlargement of thyroid with diffuse decreased density .
The thymus has a variable appearance, typically soft tissue density at birth through adolescence, reaching a maximal size by the late teens, then gradually becoming fatty replaced through adulthood. The gland can extend from the lower border of the thoracic inlet through the fourth costal cartilage anteriorly.
Thymic hyperplasia is characterized by an increase in volume of the thymus by more than 50% from baseline. The enlarged thymus can extend superiorly to the level of the thoracic inlet and into the retrovisceral space. Thymic hyperplasia can occur in many conditions, including hyperthyroidism, acromegaly, Addison’s disease, stress, chemotherapy, radiotherapy, and myasthenia gravis. The normal average thymic thickness on an inspiratory phase CT study is 1.1 cm between ages 6 and 19 years and 0.8 cm in adults older than 20 years, and an increased thickness of the thymus greater than 1.3 cm beyond age 20 should raise the suspicion for thymic hyperplasia (Fig. 22) . A hyperplastic thymus typically demonstrates a normal shape, with homogenous attenuation and signal. On MR imaging, a signal drop on the opposed-phase imaging compared to in-phase imaging indicates a normal thymus or thymic hyperplasia is present as the thymus normally contains interspersed fat . It is important to distinguish thymic hyperplasia from thymoma, which can present as asymmetry of the lobes, focal contour abnormality, or as a discrete soft tissue mass. Thymic hyperplasia demonstrates homogenous low-grade fluorodeoxyglucose (FGD) uptake, whereas thymoma has more focal FDG uptake.
There are many causes of traumatic injury to the thoracic inlet, each with unique features depending on the method of trauma and the structures involved. Importantly, trauma to the neck accounts for 5–10% of all serious traumatic injuries . The two most common forms of trauma are blunt force trauma and penetrating trauma.
Pneumomediastinum most commonly results from traumatic rupture of the trachea or esophagus, which occurs in 10% of blunt chest trauma cases, or as a result of spontaneous alveolar rupture with air dissecting from the pulmonary interstitium (Macklin effect) . Pneumomediastinum may then extend into the neck and shoulder soft tissues. Alternatively, subcutaneous air from penetrating neck injuries can dissect inferiorly causing pneumomediastinum. A careful inspection of the organs traversing the thoracic inlet is critical in penetrating injuries involving the neck and/or chest. Positive findings in one region may trigger further investigation of the other region and may help identify the etiology of pneumomediastinum. Patients with pneumomediastinum commonly present with chest/neck pain, cough, and dyspnea . On radiographs, linear lucencies surrounding the mediastinal structures indicate the presence of air, often more conspicuous on lateral radiographs. CT imaging is much more sensitive for the detection of air within the mediastinal structures and can often help to identify the cause of pneumomediastinum and look for additional sites of injury  (Fig. 23).
Vascular injuries are commonly encountered in trauma, with cervical vascular injuries present in 0.1–1.1% of all trauma cases. Common vascular injuries include transection, dissection, pseudoaneurysm, and/or thrombosis. Patients can present with ipsilateral pain to the affected side, bruit, and neurologic symptoms due to ischemia . CT angiogram in the arterial phase is the preferred modality to diagnose vascular pathology and look for signs of active extravasation. Signs of arterial injury include active extravasation, pseudo-aneurysm formation, abrupt narrowing of an artery, loss of opacification of an arterial segment, or arteriovenous fistula formation (Fig. 24).
Sternocleidomastoid muscle hematoma
Sternocleidomastoid muscle hematoma can be seen in the setting of blunt neck trauma. Large hematomas can compress the critical vascular and respiratory structures along the neck/thoracic inlet and can therefore quickly become life-threatening. Physical examination may be misleading as this condition may be mistaken for a thyroid goiter. Patients can present with varying degrees of clinical symptoms, including soft tissue swelling and pain, vital sign instability, hypotension, hypoxia, and possible respiratory arrest from compression of the trachea by the hematoma . Imaging will demonstrate asymmetric enlargement of the injured muscle with possible identification of a fluid collection and/or active extravasation of contrast within the muscle (Fig. 25). It is important to report this finding as it may necessitate intubation or neck dissection for airway protection and decompression respectively.
Endocrinological organs to consider in the region of the thoracic inlet include the parathyroid and thyroid glands. The thyroid isthmus lies just above the level of the thoracic inlet in the midline. The parathyroid glands are normally paired bilaterally, typically located posterior to the thyroid gland. However, their location can be variable, occurring anywhere along the thyrothymic tract, extending from the angle of the mandible to the lower aspect of the superior mediastinum . Abnormalities and variants of these organs are commonly reported, including thyroid nodules, thyroid pyramid, and parathyroid hyperplasia. Thyroid nodules are incidental findings in 4–8% of adults [30, 31].
Thyroid goiter is a condition in which there is enlargement of the thyroid gland due to multiple nodules with increased, decreased, or normal function. Thyroid goiters can be defined according to their location and origin: cervical goiter, retrosternal/substernal goiter, mediastinal goiter, primary goiter (origin in ectopic thyroid tissue), and secondary goiter (origin in cervical thyroid). Patients typically are asymptomatic, but may present with dyspnea and wheezing if the trachea is compressed (Fig. 26). Surgical excision is the definitive therapy for thyroid goiter. However, many do not have compressive symptoms and therefore do not require treatment. Observation is considered for small lesions and elderly patients. Radiographs may demonstrate neck base/superior mediastinal mass with or without intrinsic calcification, tracheal displacement, and tracheal narrowing. CT can help delineate the mass, which may have cystic changes, high attenuation (70–80 HU) due to intrinsic iodine and calcification. There can be prolonged and sustained enhancement after IV contrast .
Madelung disease, also known as benign symmetric lipomatosis, is a rare disease of lipodystrophy characterized by diffuse, symmetric, unencapsulated fatty accumulation most commonly in the neck, upper back, shoulder girdle, and upper extremities (Fig. 27). Fat accumulation is also seen in the deep spaces, including the deep layer of sternocleidomastoid muscles, trapezius muscles, periphery of paravertebral muscles, and surrounding the salivary glands. This process is characterized by abnormal fatty tissue metabolism causing accelerated fatty tissue proliferation. It has been associated with alcoholism and in middle-aged men of Mediterranean descent. Often asymptomatic, however, long-term lipomatous deposits can be cosmetically deforming and may compress the aerodigestive tract and great veins, causing dysphagia, dyspnea, or venous stasis . The diagnosis is typically made based on history, clinical appearance, and imaging. The definitive treatment is surgical therapy. Both CT and MRI can accurately identify the distribution and involvement of the disease, along with its sequelae including compression of surrounding organs. These imaging modalities play important roles in distinguishing Madelung disease from obesity (more diffuse process), lipoma (encapsulated lesions), and other soft tissue tumors, as well as aiding surgical planning.
As seen, the thoracic inlet is a critical landmark in radiology, as it is a central conduit for many organ systems, and thus allowing itself to a vast array of non-neoplastic pathology. It is therefore important to critically evaluate this region and be aware that it may be overlooked on imaging of the neck or chest. The thoracic inlet marks a critical junction between the neck and chest imaging. A detailed examination of this region is essential when reviewing both neck and thoracic studies. The mnemonic VINDICATE is a helpful guide to methodically create differential diagnoses for non-neoplastic pathology encountered in this region.
Availability of data and materials
Deep cervical fascia
Diffuse idiopathic skeletal hyperostosis
Deep layer of the deep cervical fascia
Internal jugular vein
Middle layer of the deep cervical fascia
Partial anomalous pulmonary venous return
Posterior cervical space
Superficial cervical fascia
Superficial layer of the deep cervical fascia
Superior vena cava
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The authors would like to acknowledge the following individuals for their contributions: Nadezhda Kiriyak for illustrated figures and Sarah Klingenberger for preparing the figures for submission.
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Nguyen, T.T., Melendez, P.E., Kaproth-Joslin, K. et al. Non-neoplastic pathology at the crossroads between neck imaging and cardiothoracic imaging. Insights Imaging 10, 116 (2019). https://doi.org/10.1186/s13244-019-0790-y
- Thoracic inlet
- Head and neck imaging
- Thoracic imaging