Management of sporadic desmoid-type fibromatosis: a European consensus approach based on patients' and professionals' expertise - a sarcoma patients EuroNet and European Organisation for Research and Treatment of Cancer/Soft Tissue and Bone Sarcoma Group initiative.

@article{Kasper2015ManagementOS,
  title={Management of sporadic desmoid-type fibromatosis: a European consensus approach based on patients' and professionals' expertise - a sarcoma patients EuroNet and European Organisation for Research and Treatment of Cancer/Soft Tissue and Bone Sarcoma Group initiative.},
  author={Bernd Kasper and Clive Baumgarten and Sylvie Bonvalot and Rick L Haas and Florian Haller and Peter Hohenberger and Guy Moreau and Winette T. A. van der Graaf and Alessandro Gronchi},
  journal={European journal of cancer},
  year={2015},
  volume={51 2},
  pages={
          127-36
        }
}
Desmoid-type fibromatosis (DF) is a rare monoclonal, fibroblastic proliferation characterised by a variable and often unpredictable clinical course. It may affect nearly all parts of the body including extremities, trunk and abdomen. Considering the variable clinical presentations, anatomic locations and biological behaviours, an individualised treatment approach is required. No established or evidence-based approach for the treatment of this neoplasm is available as of today. Therefore, we… CONTINUE READING

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