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Primary retroperitoneal soft tissue sarcoma: Imaging appearances, pitfalls and diagnostic algorithm

  • C. Messiou*
  • , E. Moskovic
  • , D. Vanel
  • , C. Morosi
  • , R. Benchimol
  • , D. Strauss
  • , A. Miah
  • , H. Douis
  • , W. van Houdt
  • , S. Bonvalot
  • *Corresponding author for this work
  • The Institute of Cancer Research
  • IRCCS Istituto Ortopedico Rizzoli - Bologna
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • Institut Curie
  • Royal Marsden NHS Foundation Trust
  • University Hospitals Birmingham NHS Foundation Trust

Research output: Contribution to journalReview articleAcademicpeer-review

Abstract

Although retroperitoneal sarcomas are rare tumours, they can be encountered by a wide variety of clinicians as they can be incidental findings on imaging or present with non specific symptoms and signs. Surgical resection can offer hope of cure and patient outcomes are improved when patients are managed in high-volume specialist centers. Failure to recognize retroperitoneal sarcomas on imaging can lead to inappropriate management in inexperienced centers. Therefore it is critical that a diagnosis of retroperitoneal sarcoma should be considered in the differential diagnosis of a retroperitoneal mass with prompt referral to a soft tissue sarcoma unit. In particular, the most common retroperitoneal sarcoma subtypes, liposarcoma and leiomyosarcoma, have characteristic imaging appearances which are discussed. This review therefore aims to set the context and guide clinicians through a diagnostic pathway for retroperitoneal masses in adults which arise extrinsic to the solid abdominal viscera.
Original languageEnglish
Pages (from-to)1191-1198
JournalEuropean journal of surgical oncology
Volume43
Issue number7
DOIs
Publication statusPublished - 1 Jul 2017
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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