A rare variant of Stewart-Treves syndrome

BMJ 2015; 350 doi: https://doi.org/10.1136/bmj.g7616 (Published 07 January 2015) Cite this as: BMJ 2015;350:g7616
  1. M Pigera, histopathology specialist registrar,
  2. M Khan, consultant histopathologist,
  3. T Mcculloch, consultant histopathologist,
  4. M Malik, dermatology specialist registrar,
  5. A Raurell, consultant plastic surgeon
  1. 1Queen’s Medical Centre, Nottingham NG7 2UH, UK
  1. Correspondence to: M Pigera marian.pigera{at}gmail.com

Stewart-Treves syndrome is characterised by angiosarcoma arising in lymphoedematous extremities. This variant was seen in an 88 year old man with angiosarcoma arising …

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