Your browser doesn't support javascript.
loading
Inflammatory myofibroblastic tumour of the lung: a reactive lesion or a true neoplasm?
Panagiotopoulos, Nikolaos; Patrini, Davide; Gvinianidze, Lasha; Woo, Wen Ling; Borg, Elaine; Lawrence, David.
Afiliação
  • Panagiotopoulos N; 1 Department of Cardiothoracic Surgery, The Heart Hospital, University College London Hospitals (UCLH), London, UK ; 2 Department of Histopathology, University College London Hospitals (UCLH), London, UK.
  • Patrini D; 1 Department of Cardiothoracic Surgery, The Heart Hospital, University College London Hospitals (UCLH), London, UK ; 2 Department of Histopathology, University College London Hospitals (UCLH), London, UK.
  • Gvinianidze L; 1 Department of Cardiothoracic Surgery, The Heart Hospital, University College London Hospitals (UCLH), London, UK ; 2 Department of Histopathology, University College London Hospitals (UCLH), London, UK.
  • Woo WL; 1 Department of Cardiothoracic Surgery, The Heart Hospital, University College London Hospitals (UCLH), London, UK ; 2 Department of Histopathology, University College London Hospitals (UCLH), London, UK.
  • Borg E; 1 Department of Cardiothoracic Surgery, The Heart Hospital, University College London Hospitals (UCLH), London, UK ; 2 Department of Histopathology, University College London Hospitals (UCLH), London, UK.
  • Lawrence D; 1 Department of Cardiothoracic Surgery, The Heart Hospital, University College London Hospitals (UCLH), London, UK ; 2 Department of Histopathology, University College London Hospitals (UCLH), London, UK.
J Thorac Dis ; 7(5): 908-11, 2015 May.
Article em En | MEDLINE | ID: mdl-26101648
ABSTRACT
Inflammatory myofibroblastic tumour (IMT) of the lung represents an extremely rare type of inflammatory pseudo tumor that appears most commonly in children and young individuals. There has been an ongoing controversy whether an IMT is a reactive lesion or a true neoplasm making the further management extremely challenging. Purpose of the paper is through a literature review to highlight the existence of this rare tumour along with its key features and the management options available.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Thorac Dis Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Thorac Dis Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Reino Unido