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DOI 10.21037/med-22-53

Медицинская библиотека · Mediastinum (Hong Kong, China) · 2023

Multimodality imaging of mediastinal masses and mimics.

Archer John Matthew, Ahuja Jitesh, Strange Chad D, Shroff Girish S, Gladish Gregory W, Sabloff Bradley S, Truong Mylene T

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A wide variety of neoplastic and nonneoplastic conditions occur in the mediastinum. Imaging plays a central role in the evaluation of mediastinal pathologies and their mimics. Localization of a mediastinal lesion to a compartment and characterization of morphology, density/signal intensity, enhancement, and mass effect on neighboring structures can help narrow the differentials. The International Thymic Malignancy Interest Group (ITMIG) established a cross-sectional imaging-derived and anatomy-based classification system for mediastinal compartments, comprising the prevascular (anterior), visceral (middle), and paravertebral (posterior) compartments. Cross-sectional imaging is integral in the evaluation of mediastinal lesions. Computed tomography (CT) and magnetic resonance imaging (MRI) are useful to characterize mediastinal lesions detected on radiography. Advantages of CT include its widespread availability, fast acquisition time, relatively low cost, and ability to detect calcium. Advantages of MRI include the lack of radiation exposure, superior soft tissue contrast resolution to detect invasion of the mass across tissue planes, including the chest wall and diaphragm, involvement of neurovascular structures, and the potential for dynamic sequences during free-breathing or cinematic cardiac gating to assess motion of the mass relative to adjacent structures. MRI is superior to CT in the differentiation of cystic from solid lesions and in the detection of fat to differentiate thymic hyperplasia from thymic malignancy.

Для цитирования: Archer John Matthew, Ahuja Jitesh, Strange Chad D, Shroff Girish S, Gladish Gregory W, Sabloff Bradley S, Truong Mylene T. Multimodality imaging of mediastinal masses and mimics.. Mediastinum (Hong Kong, China). 2023. DOI: 10.21037/med-22-53.
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