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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
- M Pigera, histopathology specialist registrar,
- M Khan, consultant histopathologist,
- T Mcculloch, consultant histopathologist,
- M Malik, dermatology specialist registrar,
- A Raurell, consultant plastic surgeon
- 1Queen’s Medical Centre, Nottingham NG7 2UH, UK
- 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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