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Mediastinal tumors
Mediastinal tumors
Mediastinal tumors
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Mediastinal tumor
Micrograph of the primitive neuroepithelium of an immature teratoma of the mediastinum. H&E stain.
SpecialtyOncology Edit this on Wikidata

A mediastinal tumor is a tumor in the mediastinum, the cavity that separates the lungs from the rest of the chest. It contains the heart, esophagus, trachea, thymus, and aorta.

The mediastinum has three main parts: the anterior mediastinum (front), the middle mediastinum, and the posterior mediastinum (back). Masses in the anterior portion of the mediastinum can include thymoma, lymphoma, pheochromocytoma, germ cell tumors including teratoma, thyroid tissue, and parathyroid lesions. Masses in this area are more likely to be malignant than those in other compartments.[1][2]

The most common mediastinal masses are thymoma (20% of mediastinal tumors), usually found in the anterior mediastinum, followed by neurogenic tumor (15–20%) located in the anterior mediastinum.[3] Lung cancer typically spreads to the lymph nodes in the mediastinum.

Masses in the posterior portion of the mediastinum tend to be neurogenic in origin, and in adults tend to be of neural sheath origin including neurilemomas and neurofibromas.[3]

Types

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Anterior Mediastinal Masses

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50% of mediastinal masses occur in the anterior compartment. The most common anterior masses are commonly known by the '4 T's' which refer to thymomas, teratomas, thyroid tissue and 'terrible' lymphomas.[4]

Thymic carcinoma and thymoma

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Main article: thymoma

The thymus is a lymphatic organ in the anterior mediastinum where lymphocytes, immune system cells, are produced and matured. It is most prominent in infants and begins to involute at 1 year of age. Tumors of this organ are the most common primary anterior mediastinal tumor, comprising 20% of all mediastinal cancers.[5] Thymomas and thymic carcinomas most commonly occur between ages 40 and 60 and only rarely occur in children. Patients usually initially present with an incidental finding on imaging, symptoms due to compressive effects or symptoms due to an associated paraneoplastic syndrome such as myasthenia gravis. Half of patients with a thymoma are found to have myasthenia gravis, an autoimmune disorder presenting with diplopia, ptosis, dysphagia, weakness or fatigue.[6]

Both thymic tumors originate from thymic epithelial cells. Under microscope, thymomas have lobulations with bands of fibrous stroma, while thymic carcinomas lack lobulated architecture and have more cystic and necrotic changes.[7] Thymomas can develop into carcinomas, although this only occurs after about a decade.[4] Diagnosis is achieved through CT or MRI of the chest, which can differentiate between other mediastinal masses. Treatment may include chemoradiotherapy, immunotherapy, and/or surgical resection.[7]

Lymphoma

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Main article: lymphoma
Micrograph of a primary mediastinal large B-cell lymphoma, a rare type of lymphoma that arises in the mediastinum. H&E stain.

Lymphomas comprise 15% of primary mediastinal masses and 45% of anterior mediastinal masses in children. The most common are nodular sclerosing Hodgkin lymphoma, primary mediastinal large B-cell lymphoma and lymphoblastic lymphoma. Most are seen in the anterior compartment and rest are seen in middle compartment. Hodgkin's lymphoma usually present in 40–50's with nodular sclerosing type (7), and non-Hodgkin's appears in all age groups. There is also primary mediastinal B-cell lymphoma with exceptionally good prognosis.[8][9][10]

Common symptoms of a mediastinal lymphoma of include fever, weight loss, night sweats, and compressaive symptoms such as pain, dyspnea, wheezing, Superior vena cava syndrome, pleural effusions. Diagnosis is usually by CT or MRI showing lobulated mass. Confirmation done by tissue biopsy of accompanying nodes if any, mediastinoscopy, mediastinotomy, or thoracotomy. FNA biopsy is usually not adequate. Treatment of mediastinal Hodgkin's involves chemotherapy and/or radiation. Prognosis is variable and dependent on the lymphoma type and staging. Stage 1 and 2a Hodgkin lymphoma has a good prognosis with 5-year overall survival of 90%.

Germ Cell Tumors

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Main article: Mediastinal germ cell tumor

Germ cell tumors comprise 15% of mediastinal masses and usually affect young adult men between the ages of 18 and 29. These are rare tumors that develop from reproductive cells that grow in the chest instead of the gonads during early development. These tumors resemble testicular germ cell tumors and are classified into three types: teratomas, seminomas, and non-seminomatous tumors such as yolk sac tumors or embryonal carcinomas[11]. Teratomas are the most common type to form in the mediastinum.

Tumors are initially asymptomatic but may cause chest pain, cough, or shortness of breath when the size causes compression on surrounding structures. The tumor is diagnosed by CT and MRI scans as well as blood markers like AFP, β-hCG and LDH that help classify the type of germ cell tumor.[11] Most teratomas are benign tumors but require close follow-up and treatment. Teratomas are associated with Klinefelter syndrome.Teratomas are usually noncancerous and treated with surgery, while seminomas and non-seminomatous tumors are more aggressive and treated with chemotherapy and surgery.[12] The outlook depends on the tumor classification, with seminomas and teratomas having excellent prognosis and non-seminomatous tumors having a higher chance of metastasis.[13]

Diagnosis

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In several editions of Physical Diagnosis,[14] concerning mediastinal tumors the author writes:

According to Christian1 the mediastinal neoplasms which are neither so rare nor so obscure as to make diagnosis practically impossible are: (1) Sarcoma (including lymphosarcoma, leucaemic growths, and Hodgkins' disease; (2) Teratoma and cyst.

Many signs and symptoms of a mediastinal tumor do not distinguish between these two principal classes of mediastinal tumor. However, on a radiograph usually the former class will have an irregular shape and the latter class will have a smooth spherical or ovoid shape. A large minority of patients with a mediastinal teratoma (including dermoid cyst) will cough up hair.[14] For a differential diagnosis, the key is to exclude aneurysm.[citation needed]

See also

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia

Mediastinal tumors

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Mediastinal tumors are abnormal growths that arise in the mediastinum, the central compartment of the thoracic cavity located between the lungs, extending from the inlet of the thorax to the diaphragm and containing vital structures such as the heart, great vessels, esophagus, trachea, and thymus. These tumors can be benign or malignant, originating from various tissues including thymic, lymphatic, neural, or germ cell elements, and they represent a diverse group of neoplasms that may be asymptomatic or cause significant morbidity due to their location. The is anatomically divided into three compartments—anterior, middle, and posterior—each associated with characteristic tumor types that reflect the predominant tissues present. In the anterior mediastinum, which accounts for approximately 50% of cases, common tumors include thymomas (the most frequent primary malignancy, comprising about 20% of mediastinal cancers), lymphomas (such as Hodgkin and non-Hodgkin types), and tumors like teratomas or seminomas. The middle mediastinum often harbors benign lesions such as bronchogenic or pericardial cysts, as well as metastatic or rare primary tumors like tracheal neoplasms. Posterior mediastinal tumors predominate in children and are typically neurogenic, with such tumors constituting over 60% of masses in this region, including schwannomas, neurofibromas, or neuroblastomas, about 30% of which prove malignant. Overall, mediastinal tumors are rare, affecting fewer than 1% of the general population and peaking in incidence between ages 30 and 50, though pediatric cases are more likely to involve the posterior compartment. Many mediastinal tumors are discovered incidentally on routine chest imaging, with up to 50% remaining asymptomatic until advanced. When symptoms occur, they result from compression or invasion of adjacent structures and may include persistent cough, chest pain, shortness of breath, dysphagia, hoarseness, or superior vena cava syndrome in anterior lesions; about 25% of all mediastinal masses are malignant, with malignancy rates higher in adults (up to 60% in the anterior compartment). Diagnosis typically begins with chest radiography, followed by computed tomography (CT) or magnetic resonance imaging (MRI) for characterization, and may involve biopsy via mediastinoscopy or endobronchial ultrasound-guided sampling; tumor markers such as alpha-fetoprotein or beta-human chorionic gonadotropin aid in identifying germ cell tumors. Treatment is tailored to the tumor's , location, and , with surgical resection offering the best outcomes for resectable benign and early-stage malignant lesions, such as thymomas, where complete removal yields favorable prognosis. Malignant tumors like lymphomas or nonseminomatous tumors often require multimodality therapy, including and radiotherapy, with 5-year survival rates varying widely from 94% for localized thymomas to around 45% for malignancies. Complications can arise from tumor growth, such as or , or from interventions like postoperative infections or radiation-induced .

Anatomy of the Mediastinum

Divisions

The , the central thoracic compartment, is traditionally divided into four anatomical regions to facilitate the localization of structures and pathologies: the superior and the three subdivisions of the inferior —namely, the anterior, middle, and posterior compartments. The superior lies above the extending from the anteriorly to the T4-T5 posteriorly, bounded superiorly by the thoracic inlet, laterally by the mediastinal pleura, anteriorly by the manubrium of the , and posteriorly by the upper ; it encompasses structures such as the , trachea, , and great vessels including the . The inferior , below this plane and extending to the diaphragm, is further subdivided based on relational . Within the inferior mediastinum, the anterior compartment is situated between the sternum anteriorly and the pericardium or ascending aorta posteriorly, bounded laterally by the pleural reflections and inferiorly by the diaphragm; it primarily contains loose connective tissue, remnants of the thymus, and lymphatic structures. The middle compartment occupies the space around the heart and great vessels, bounded anteriorly by the pericardium, posteriorly by the posterior aspect of the trachea and main bronchi, laterally by the pleura, superiorly by the transverse plane, and inferiorly by the diaphragm. The posterior compartment extends behind the pericardium to the vertebral column, bounded anteriorly by the posterior pericardium and heart, laterally by the mediastinal pleura, superiorly by the transverse plane, posteriorly by the thoracic vertebrae from T5 to T12, and inferiorly by the diaphragm; it includes the descending thoracic aorta, esophagus, azygos venous system, and thoracic duct. The classification of mediastinal divisions has evolved significantly since the early , when initial schemes relied on non-anatomic boundaries derived from lateral chest radiographs, such as those proposed by Felson and others, which often used arbitrary lines like the anterior cardiac border or carinal level to separate compartments. These early models, developed in the mid- for radiographic interpretation, divided the into three or four zones but suffered from inconsistencies in and poor correlation with cross-sectional . By the late , the four-compartment model gained prominence in and for its practical utility in localizing masses. In the 2010s, the International Thymic Malignancy Interest Group (ITMIG) introduced a standardized three-compartment to address these limitations, particularly for improving diagnostic precision in mediastinal tumors using multidetector computed . This modern ITMIG model eliminates the superior compartment as a distinct entity, instead integrating its contents into the overall framework, and defines prevascular (anterior), visceral (middle), and paravertebral (posterior) compartments with CT-based boundaries: the prevascular extends from the thoracic inlet superiorly to the diaphragm inferiorly, bounded anteriorly by the , laterally by the parietal pleura, and posteriorly by the anterior ; the visceral compartment shares superior and inferior limits but is bounded anteriorly by the prevascular posterior margin and posteriorly by a vertical line 1 cm behind the anterior vertebral margin; and the paravertebral compartment is bounded anteriorly by this visceral posterior line, extending to the posterior chest wall at the transverse processes. Adopted widely since its proposal in 2014, the ITMIG enhances multidisciplinary communication and guides and surgical planning by aligning with contemporary imaging.

Key structures

The , divided into anterior, middle, and posterior compartments, contains a variety of critical organs, vessels, nerves, and tissues that occupy these spaces. The anterior mediastinum, located between the and , primarily includes the gland, which is prominent in early life and involutes with age; scattered lymph nodes; the internal mammary (thoracic) vessels, which supply the anterior chest wall; and and fat that fill the remaining space. These structures relate to the superior mediastinum above, as defined by thoracic inlet boundaries. In the middle mediastinum, bounded by the pericardium, key contents encompass the heart and its enclosing pericardium; the ascending and descending portions of the aorta; the superior and inferior vena cava; the trachea and main bronchi; and associated lymph nodes. Major nerves such as the phrenic and vagus traverse this region, alongside the pulmonary trunk and veins. The posterior mediastinum, situated behind the pericardium and extending to the diaphragm, houses the esophagus; the descending thoracic aorta; the azygos and hemiazygos veins; the thoracic duct, which serves as the primary lymphatic conduit; the sympathetic chain; the vagus nerve; and spinal cord nerve roots. Mediastinal lymphatic drainage follows patterned pathways through specialized node groups, facilitating the transport of lymph from thoracic viscera to the systemic circulation via the thoracic duct or right lymphatic duct. Anterior mediastinal nodes drain the thymus, pericardium, and anterior chest wall, converging toward internal mammary or brachiocephalic nodes; middle mediastinal nodes collect from the heart, lungs, and bronchi, linking to tracheobronchial nodes; and posterior mediastinal nodes handle drainage from the esophagus and posterior thoracic structures, emptying into the thoracic duct. These interconnected chains enable efficient fluid and cellular movement, playing a key role in the potential dissemination of pathological entities like tumors through nodal progression.

Epidemiology

Incidence and demographics

Mediastinal tumors are rare neoplasms, accounting for approximately 3% of all thoracic tumors. Their overall incidence is low, with exact rates varying by subtype and region; for example, thymomas have an incidence of about 2 cases per million annually. This low underscores their status as uncommon entities, with most cases identified through advanced diagnostic imaging rather than population-based screening. Demographically, mediastinal tumors most commonly affect individuals between and 60 years of age, with a mean presentation age around 40 to 50 years in adults. Children and adolescents are more likely to develop posterior compartment tumors, such as neurogenic types, while adults predominate in anterior compartment lesions like thymomas, which peak in the 40- to 60-year-old range. distribution is generally similar between s and females overall, though certain subtypes show variations, including a slight predominance in germ cell tumors. In terms of anatomical distribution, anterior mediastinal tumors comprise 40% to 50% of cases, middle compartment lesions account for 10% to 20%, and posterior tumors make up 25% to 30%. Approximately 65% of mediastinal tumors are benign, while 35% are malignant, with the benign-to-malignant ratio influenced by compartment—higher malignancy rates in the anterior mediastinum compared to the posterior. Incidence trends for mediastinal tumors have remained stable over recent decades, but detection rates have increased since the due to widespread use of computed tomography and , leading to more incidental findings; geographic variations exist, with slightly higher rates reported in Asian populations compared to Western ones as of 2024. This improved imaging has enhanced early identification without altering the underlying epidemiological patterns.

Risk factors and etiology

The etiology of mediastinal tumors remains largely idiopathic, with no definitive environmental or genetic causes identified for most cases. Unlike lung tumors, which are strongly associated with tobacco exposure as a primary , mediastinal tumors exhibit minimal links to , reflecting their more frequent origins in congenital, developmental, or dysregulated cellular processes within the mediastinal structures. For thymic tumors such as , the pathogenesis involves abnormal proliferation, often linked to autoimmune dysregulation; notably, 30-50% of thymoma patients develop , an autoimmune neuromuscular disorder, suggesting shared immunological mechanisms. Potential risk factors include prior to the upper chest, though this association is unconfirmed and based on limited epidemiological data. Lymphomas arising in the mediastinum, particularly non-Hodgkin lymphomas, are frequently tied to states of ; human immunodeficiency virus () infection elevates the risk of non-Hodgkin lymphoma by 60-200 times compared to the general population, while post-transplant similarly predisposes individuals through impaired immune surveillance. Epstein-Barr virus (EBV) infection contributes to lymphomagenesis in a subset of these cases, particularly in immunocompromised hosts, by promoting B-cell proliferation. Certain mediastinal tumors have genetic underpinnings, including rare familial clusters; neurogenic tumors in the posterior mediastinum, such as neurofibromas, occur more frequently in type 1 (NF1) due to mutations in the NF1 gene on 17q11, leading to uncontrolled sheath growth. Paragangliomas may arise in the context of (MEN) type 2 syndrome, driven by RET proto-oncogene mutations that enhance catecholamine-producing . Overall, these genetic associations are uncommon, affecting a minority of cases.

Clinical Presentation

Symptoms

Mediastinal tumors frequently present with symptoms attributable to local on surrounding structures or, less commonly, systemic involvement. Approximately 30-50% of patients are at , with tumors discovered incidentally during for unrelated conditions. Among those who are symptomatic, the most common manifestations include , dyspnea, and , resulting from compression of the airways, lungs, or pleura. The specific symptoms often depend on the tumor's location within the . Anterior mediastinal tumors may cause due to vascular compression, leading to facial edema in approximately 10% of cases, along with upper body swelling and distended neck veins. Middle mediastinal tumors can compress the , resulting in hoarseness or voice changes. Posterior mediastinal tumors frequently produce from spinal or neural involvement and due to esophageal compression. Malignant mediastinal tumors may additionally elicit systemic symptoms such as unintentional and fever, reflecting tumor burden or inflammatory response. Paraneoplastic syndromes occur in certain cases, notably with thymomas, where symptoms of —such as muscle weakness, fatigability, ptosis, and —affect 30-50% of patients. The onset of symptoms is typically insidious and progressive, though acute presentation can arise from complications like hemorrhage or infection within cystic lesions. These symptoms may correlate with observable physical signs, such as altered breath sounds or neck swelling, during clinical examination.

Physical examination findings

Physical examination in patients with mediastinal tumors is frequently unremarkable, particularly during early stages when tumors are small and . However, as tumors enlarge and compress surrounding structures, location-specific signs may emerge, aiding in clinical suspicion. In anterior mediastinal tumors, develops in up to 10% of cases, presenting with jugular venous distention, facial plethora, and upper extremity from venous compression. Respiratory assessment may disclose decreased breath sounds due to or , or from airway narrowing in compressive lesions. Posterior apical tumors, often neurogenic, can cause Horner syndrome, characterized by ipsilateral ptosis, , and anhidrosis secondary to sympathetic chain disruption. Cardiovascular evaluation occasionally reveals muffled in middle mediastinal masses from direct compression or associated . , an exaggerated inspiratory drop in systolic , is uncommon but may arise in rare instances of pericardial tamponade-like physiology. Additional observations include palpable cervical or supraclavicular , especially in lymphomas or other malignancies. Digital clubbing appears in select chronic cases, such as intrathoracic . No distinctive abdominal signs are typically associated with these tumors.

Diagnostic Approaches

Imaging techniques

Imaging of mediastinal tumors begins with chest radiography, which serves as the initial screening modality and often detects abnormalities incidentally during evaluation for unrelated symptoms. A widened is a common finding in cases with substantial mass effect, while chest identifies large masses through signs such as the , hilum overlay, or disruption of normal mediastinal contours. Advanced cross-sectional imaging is essential for precise characterization and localization within the anterior, middle, or posterior compartments. Computed tomography (CT) with intravenous contrast is considered the gold standard, enabling comprehensive evaluation of tumor size, precise anatomical location, degree of invasion into adjacent structures like the heart or great vessels, and enhancement patterns indicative of vascularity or necrosis. Magnetic resonance imaging (MRI) excels in assessing soft-tissue details and is particularly superior for detecting neural foraminal involvement or spinal extension in posterior mediastinal lesions, as well as differentiating tissue types through signal intensity and chemical shift sequences. Positron emission tomography-computed tomography (PET-CT) plays a key role in staging suspected malignancies and distinguishing benign from malignant tumors based on fluorodeoxyglucose (FDG) uptake, with higher avidity often correlating with aggressive histology. Clinical guidelines emphasize a stepwise approach to imaging. The American College of Radiology (ACR) Appropriateness Criteria (2021) rate CT chest with contrast as usually appropriate for initial characterization of suspected mediastinal masses, recommending MRI or PET-CT as adjuncts for indeterminate findings or when assessing or metabolic activity. Despite their utility, imaging modalities have inherent limitations that must be considered. CT exposes patients to , which is a concern in younger individuals or those requiring serial scans, while MRI is limited by higher costs, longer scan times, and contraindications such as pacemakers. Incidental detection of mediastinal masses occurs in approximately 0.5-1% of routine chest CT examinations, often necessitating further evaluation to rule out . Abnormal imaging findings typically guide subsequent for histopathological confirmation.

Biopsy and histopathological diagnosis

Biopsy of mediastinal tumors is typically pursued when suggests a requiring tissue confirmation, particularly if surgical resection is not immediately feasible or to distinguish benign from malignant processes. Common invasive techniques include CT-guided needle , mediastinoscopy, endoscopic ultrasound-guided (EUS-FNA), and video-assisted thoracoscopic surgery (VATS), each selected based on tumor location and accessibility. These methods provide tissue for histopathological analysis, enabling definitive diagnosis in the majority of cases. CT-guided percutaneous needle biopsy is a minimally invasive approach often used for accessible mediastinal masses, achieving diagnostic yields of 77-96% depending on lesion type and location. For anterior mediastinal lesions, such as thymic neoplasms, the yield is particularly high at around 91%, with core needle techniques preferred over for obtaining adequate histological samples. Mediastinoscopy, an anterior surgical approach via cervical incision, offers high sensitivity of 80-95% for sampling anterior compartment structures like lymph nodes or thymic tumors, making it valuable for staging and . EUS-FNA targets middle and posterior mediastinal lesions via transesophageal access, with diagnostic yields of 85-97% reported, especially effective for subcarinal or paratracheal masses. VATS provides direct visualization and for peripheral or middle/posterior tumors, serving as a reliable diagnostic tool when less invasive methods are inconclusive. Histopathological diagnosis relies on the (WHO) classification, with the 2021 fifth edition updating criteria for thymic epithelial tumors, including thymomas, thymic carcinomas, and neuroendocrine neoplasms, to incorporate morphological, , and molecular features. plays a key role in differentiation; for instance, cytokeratins (e.g., AE1/AE3) highlight epithelial components in thymomas, while CD20 positivity aids in identifying B-cell lymphomas common in the anterior mediastinum. Molecular markers, such as KIT mutations (primarily in exon 17), are relevant in certain mediastinal tumors and thymic carcinomas, informing and potential. These procedures carry risks, including (5-15% incidence in percutaneous biopsies, often requiring placement in severe cases), , , or . Biopsies are indicated primarily when preoperative confirmation of is needed to guide nonsurgical or when patients are poor surgical candidates, avoiding unnecessary risks in resectable cases. Integration of biopsy results with achieves preoperative diagnostic resolution in approximately 90% of mediastinal tumor cases, facilitating tailored .

Classification and Types

Anterior mediastinal tumors

Anterior mediastinal tumors comprise approximately 50% of all mediastinal masses. These masses are diverse, with thymic malignancies accounting for about 35% and lymphomas for 25%, while or endocrine tumors represent 15%, benign teratomas 10%, malignant tumors 10%, and benign thymic lesions 5%. Although two-thirds of all mediastinal masses are benign overall, anterior compartment masses have a higher rate, with roughly 59% being malignant. The most prevalent type is or thymic , originating from epithelial cells and constituting 35-50% of anterior mediastinal tumors. These are staged using the ninth edition TNM classification system for thymic epithelial tumors (effective January 2025), which defines stages from I (no invasion beyond the ) to IV (distant ). Thymomas typically appear encapsulated in early stages but become invasive in later stages, involving surrounding mediastinal structures. Lymphomas, making up 20-25% of cases, include both (about 13%) and (about 12%), with non-Hodgkin variants predominantly in origin, such as primary mediastinal large . These exhibit rapid growth, often forming bulky masses that may encroach on adjacent structures without clear encapsulation. Germ cell tumors account for approximately 20% of anterior mediastinal tumors, including benign teratomas and malignant forms like seminomas; the was updated in the 5th edition of the WHO tumor (2024), emphasizing biochemical markers and unified nomenclature. Teratomas are often heterogeneous, containing elements such as fat, fluid, and , while seminomas present as , bulky lesions. Extensions from or parathyroid glands, such as goiters or adenomas, comprise about 10-15% and typically arise from superior mediastinal involvement. A notable feature of anterior mediastinal tumors, particularly s, is their association with autoimmune disorders; for instance, pure red cell aplasia occurs in approximately 5% of thymoma cases.

Middle mediastinal tumors

Middle mediastinal tumors account for approximately 10-20% of all mediastinal masses and are predominantly associated with visceral structures such as the heart, trachea, bronchi, and lymph nodes. Unlike tumors in other compartments, those in the middle mediastinum are often benign, with cystic lesions comprising up to 40% of cases, while solid tumors represent the remainder and may include reactive or malignant processes. The most common type is bronchogenic cysts, which are congenital malformations arising from anomalous budding of the ventral during embryogenesis and account for about 50% of middle mediastinal cysts. These fluid-filled, thin-walled structures are typically located near the trachea or main bronchi, remain in most cases unless infected or causing compression, and are lined by ciliated with cartilage or smooth muscle components. constitutes around 30% of middle mediastinal masses, often reactive due to infections or granulomatous diseases like , presenting as enlarged nodes that can be unilateral or bilateral; malignant involvement may occur in lymphomas or metastases. Cardiac tumors are rare, comprising less than 1% of mediastinal tumors, with examples including atrial myxomas that originate from endocardial tissue, exhibit a pedunculated morphology, and carry a risk of systemic . Other infrequent entities include sarcomas or metastatic deposits from distant primaries. Middle mediastinal tumors frequently mimic primary pathologies on due to their proximity to pulmonary structures, potentially leading to misdiagnosis as parenchymal lesions. Recent 2023 studies have emphasized the role of endobronchial ultrasound (EBUS) in enhancing detection and characterization of these lesions, particularly for sampling and cystic structures in the central airways. While some middle mediastinal masses may overlap with posterior compartment neurogenic tumors at the boundaries, detailed neurogenic features are addressed elsewhere.

Posterior mediastinal tumors

Posterior mediastinal tumors account for approximately 25-30% of all mediastinal neoplasms. These tumors are predominantly benign, with about 70% exhibiting non-malignant behavior overall, though rates are higher in pediatric cases due to aggressive subtypes. Neurogenic tumors constitute the majority, comprising 60-75% of posterior mediastinal masses, and arise from neural crest-derived tissues within the paravertebral gutters. The primary types include neurogenic neoplasms, which predominate in this compartment. In adults, schwannomas and neurofibromas are most common, often presenting as encapsulated, slow-growing lesions that may adopt a dumbbell shape due to extension through intervertebral foramina into the . In children, and prevail, with being particularly aggressive and associated with bone metastases in 20-30% of cases at diagnosis. Paragangliomas represent a rare subtype, typically functional and secreting catecholamines, leading to symptoms like ; they are occasionally linked to von Hippel-Lindau syndrome. Esophageal duplication cysts, considered developmental anomalies rather than true neoplasms, also occur here as benign foregut malformations. Overall, approximately 30% of posterior mediastinal tumors are malignant, reflecting the influence of pediatric neuroblastomas and occasional malignant nerve sheath tumors. These lesions often involve anatomical structures such as the sympathetic chain or , contributing to their characteristic posterior location.

Management

Surgical interventions

Surgical intervention is the primary treatment modality for benign mediastinal tumors and resectable malignant tumors, particularly when complete resection (R0) can be achieved to optimize outcomes. This approach is indicated for tumors causing symptomatic compression, those suspected of , or lesions amenable to curative intent, as surgical removal addresses both diagnostic and therapeutic needs with relatively low associated morbidity. For instance, in cases of thymomas, which predominate in the anterior mediastinum, total is standard to ensure comprehensive clearance. The choice of surgical approach depends on tumor location, size, and invasion. provides optimal exposure for anterior mediastinal lesions, facilitating en bloc resection of invasive tumors involving adjacent structures like the great vessels. For posterior or lateral tumors, remains traditional, but (VATS) has become the preferred minimally invasive option in over 20% of cases, particularly for benign lesions, offering reduced hospital stays and comparable oncologic results. Robotic-assisted thoracoscopic surgery (RATS), emerging prominently since the , enhances precision through three-dimensional visualization and articulated instruments, leading to shorter postoperative recovery times and lower conversion rates to open procedures compared to conventional VATS. Symptomatic cysts may require targeted drainage alongside resection to alleviate pressure on surrounding structures. Complications occur in approximately 5-17% of cases, including injury leading to diaphragmatic dysfunction, hemorrhage requiring reoperation, and prolonged ventilation, though rates are lower with minimally invasive techniques. is less than 1% in high-volume centers experienced with these procedures, reflecting improvements in perioperative care. Recent advances, aligned with 2025 guidelines, emphasize for stage III thymomas to downstage tumors and improve resectability prior to surgery, while VATS achieves complete resection in over 90% of benign cases with minimal morbidity.

Nonsurgical treatments

Nonsurgical treatments for mediastinal tumors primarily encompass , , targeted therapies, , and supportive care, employed either as primary modalities for unresectable cases or in and adjuvant settings to facilitate surgical resection or control disease progression. These approaches are tailored based on tumor , stage, and location within the , with indications including for locally advanced cases and palliative management for metastatic disease. Chemotherapy serves as the cornerstone for lymphomas originating in the mediastinum. For , the regimen (, , , ) is standard, achieving complete response rates of 80-90% in early-stage disease involving the mediastinum. In non-Hodgkin lymphomas, such as primary mediastinal large , R-CHOP (rituximab, , , , ) yields response rates of 80-90%, often used as frontline therapy. For advanced thymomas and tumors, neoadjuvant is indicated to downstage tumors; platinum-based regimens like BEP (, , ) are employed for seminomatous tumors, with response rates supporting subsequent resection in select cases. Radiation therapy is commonly utilized in adjuvant settings following incomplete resection of thymomas, with doses of 45-60 Gy to the mediastinal bed reducing local recurrence rates. For lymphomas, involved-field radiation targets residual disease after chemotherapy, typically at 30-36 Gy, to consolidate remission while minimizing toxicity to surrounding structures. Emerging applications include stereotactic body radiation therapy (SBRT) for small posterior mediastinal tumors, such as neurogenic lesions, offering precise high-dose delivery with favorable local control and low morbidity in inoperable patients. Targeted therapies and immunotherapies are increasingly integrated for specific histologies. PD-L1 inhibitors, such as pembrolizumab, received FDA approval in 2022 for advanced thymic carcinoma based on objective response rates of around 20% in pretreated patients, with ongoing evaluations extending to 2023 data. Rituximab, a monoclonal antibody targeting CD20, is a key component of regimens for CD20-positive lymphomas, enhancing response durability when combined with chemotherapy. As of 2025, chimeric antigen receptor T-cell (CAR-T) therapies, including lisocabtagene maraleucel, demonstrate efficacy in refractory B-cell lymphomas, with complete response rates of 40-60% in relapsed primary mediastinal cases, representing a significant update for salvage settings. No standardized targeted options exist yet for neurogenic tumors. Supportive measures play a vital role in managing complications, particularly superior vena cava (SVC) syndrome associated with anterior mediastinal masses, where corticosteroids like dexamethasone are administered to alleviate and improve symptoms rapidly prior to definitive therapy.

Prognosis and Outcomes

Survival rates by type

Mediastinal tumors exhibit variable survival rates depending on their histological type and location, with overall 5-year survival rates approximately 88% across all cases, while malignant tumors have rates around 71%; benign tumors generally achieve survival exceeding 95% following resection. Survival outcomes differ significantly by tumor type. For thymomas, primarily located in the anterior mediastinum, 5-year survival rates reach 80% to 90% for Masaoka stages I and II, dropping to approximately 50% for stage IV . Primary mediastinal B-cell lymphomas, also anterior, demonstrate 5-year rates of 85% to 95% with chemotherapy-based regimens. tumors show favorable outcomes for seminomas at 90% 5-year , whereas nonseminomatous variants have rates around 70%. In the posterior mediastinum, benign neurogenic tumors yield 95% post-resection, but pediatric s have 5-year rates of 50% to 70%, particularly in high-risk cases. Key prognostic factors include tumor stage, with the Masaoka staging system particularly influential for thymomas; resectability, where complete surgical removal markedly improves outcomes; histological classification per WHO grades, as higher-grade tumors correlate with poorer ; and patient age, with individuals under 40 years exhibiting better survival across types. Survival trends have improved by 10% to 15% since 2010, attributable to multimodal therapies combining , , and radiation; emerging therapies, including , are further enhancing outcomes as of 2025. Recent data from the SEER database indicate an overall 5-year survival of 75% for thymic epithelial tumors, reflecting these advances.

Follow-up and surveillance

Follow-up and surveillance for patients with mediastinal tumors aim to detect recurrence early, monitor for treatment-related complications, and assess , with protocols tailored to tumor type, stage, and risk factors. Recurrence rates vary widely by tumor type, underscoring the need for vigilant monitoring to enable prompt intervention. Risk-stratified approaches, as recommended by the (NCCN) guidelines version 2.2025, adjust frequency based on factors such as resection completeness and to balance detection efficacy with minimizing . General post-treatment surveillance typically involves contrast-enhanced chest computed tomography (CT) or magnetic resonance imaging (MRI) every 6 to 12 months for the first 2 years, followed by annual up to 5 to 10 years, depending on tumor . Clinical evaluations, including , , and laboratory tests, occur at each visit to identify symptoms of recurrence or late effects, such as radiation-induced . Quality of life assessments, using validated tools like the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire, are integrated to evaluate long-term impacts on respiratory function, neurological status, and psychological well-being. Management of late effects includes multidisciplinary care for issues like cardiac from or chemotherapy-induced neuropathy. For thymomas and thymic carcinomas, surveillance is guided by the NCCN Thymomas and Thymic Carcinomas guidelines version 2.2025. In completely resected stage I thymomas without capsular invasion, chest CT with contrast is recommended every 6 to 12 months for 2 years, then annually up to 10 years; for all other thymomas, occurs every 6 months for 2 years, then annually up to 10 years. Thymic carcinomas follow a more intensive schedule: every 3 to 6 months for 2 years, then annually up to 5 years for higher-risk cases. MRI may replace CT in contrast-intolerant patients or younger individuals to reduce cumulative dose. No routine tumor markers are used. In tumors, particularly nonseminomatous types, tumor markers such as (AFP) and beta-human chorionic (bHCG) are monitored if elevated pre-treatment, typically monthly for 6 months post-therapy, then every 3 months for up to 2 years. with CT or MRI assesses residual masses after , with schedules of every 3 to 6 months initially, transitioning to annually beyond 2 years if markers normalize. For seminomas, positron emission -computed (PET-CT) evaluates response, followed by less frequent based on risk. These protocols align with International Cancer Collaborative Group classifications, emphasizing marker normalization before considering surgical resection of residuals. For lymphomas, such as primary mediastinal large B-cell lymphoma, the NCCN B-Cell Lymphomas guidelines version 3.2025 recommend PET-CT at the end of treatment to confirm response, followed by clinical monitoring with physical exams and labs every 3 to 6 months for 2 years, then every 6 to 12 months through year 5, and annually thereafter. Routine surveillance imaging is not mandated beyond end-of-treatment PET unless symptoms arise or for high-risk features, focusing instead on detecting late relapses, which are uncommon after 5 years. Neurogenic tumors, often benign in adults, require tailored surveillance post-resection. For benign lesions like schwannomas or neurofibromas, clinical follow-up suffices without routine imaging if complete excision is achieved, though MRI is advised every 1 to 2 years initially if involvement was present to monitor for rare regrowth. Malignant neurogenic tumors, such as neuroblastomas or sarcomas, warrant CT or MRI every 6 months for 2 years, then annually up to 5 years, with emphasis on neurological assessments for complications like Horner syndrome recurrence. Long-term imaging is generally not required for benign cases due to low recurrence risk.

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