Literature DB >> 22836457

Management of desmoid-type fibromatosis involving peripheral nerves.

Mario G Siqueira1, Paulo L Tavares, Roberto S Martins, Carlos O Heise, Luciano H L Foroni, Marcelo Bordalo, Roberto Falzoni.   

Abstract

Desmoid-type fibromatosis is an uncommon and aggressive neoplasia, associated with a high rate of recurrence. It is characterized by an infiltrative but benign fibroblastic proliferation occurring within the deep soft tissues. There is no consensus about the treatment of those tumors. We present a surgical series of four cases, involving the brachial plexus (two cases), the median nerve and the medial brachial cutaneous nerve. Except for the last case, they were submitted to multiple surgical procedures and showed repeated recurrences. The diagnosis, the different ways of treatment and the prognosis of these tumoral lesions are discussed. Our results support the indication of radical surgery followed by radiotherapy as probably one of the best ways to treat those controversial lesions.

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Year:  2012        PMID: 22836457     DOI: 10.1590/s0004-282x2012000700008

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  2 in total

1.  A Rare Case of Extra-abdominal Desmoid-type Fibromatosis Arising from the Popliteal Fossa.

Authors:  Mantu Jain; Sudhanshu S Das; Amrit Gantaguru; Ritesh Panda; Sudarsan Behera
Journal:  Cureus       Date:  2018-11-28

2.  Desmoid tumour of the brachial plexus.

Authors:  Orege Juliette; Koech Florentius; Ndiangui Francis; Benson Ndegwa Macharia; Mbaruku Neema
Journal:  Case Rep Surg       Date:  2013-06-12
  2 in total

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