Mesenchymal Tumors of the Mediastinum

David I. Suster, A. Craig Mackinnon, Jitesh Ahuja, Patricia M. de Groot, Mylene T. Truong

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Mesenchymal tumors of the mediastinum are relatively rare; however, almost all types of mesenchymal lesions have been reported in this anatomic compartment. This includes vascular tumors, fibroblastic/fibrohistiocytic tumors, neurogenic tumors, myogenic tumors, lipomatous tumors, bone and cartilaginous tumors, and other tumors of uncertain etiology or histogenesis. These tumors cover the spectrum from benign to malignant neoplasms. The anatomic division of the mediastinum into three compartments, anterior, middle, and posterior, is helpful in certain instances when approaching these tumors; for example, neurogenic tumors are known to preferentially arise in the posterior mediastinum. In most cases these tumors share similar histologic and molecular genetic alterations to their soft tissue counterparts. Clinically the tumors may behave in slightly different manner as these lesions may sometimes grow and displace thoracic structures before becoming symptomatic. The diagnosis of these tumors often requires clinical, radiologic, and histologic correlation and in many cases will require ancillary diagnostic testing to secure the diagnosis.

Original languageEnglish
Title of host publicationThe Thorax
Subtitle of host publicationMedical, Radiological, and Pathological Assessment
PublisherSpringer International Publishing
Pages197-219
Number of pages23
ISBN (Electronic)9783031210402
ISBN (Print)9783031210396
DOIs
StatePublished - 1 Jan 2023
Externally publishedYes

Keywords

  • Bone and soft tissue
  • Mediastinum
  • Mesenchymal
  • Sarcoma
  • Thymus

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