S�zary-type cutaneous T-cell leukaemia. Response to Winkelmann regimen.
DOI:
https://doi.org/10.2340/0001555570251253Abstract
A 37-year-old woman presented with an aggressive leukaemic form of small T-cell Sézary syndrome. Despite this unusually malignant variant of the disease, there was a dramatic response to a modified Winkelmann regimen of chlorambucil and prednisolone, and a useful, sustained remission of 7 months. The Winkelmann regimen remains an important and relatively non-toxic chemotherapeutic option for palliation of advanced Sézary syndrome.Downloads
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Published
1990-05-01
How to Cite
Harland, C. C., Balsitis, M., & Millard, L. G. (1990). S�zary-type cutaneous T-cell leukaemia. Response to Winkelmann regimen. Acta Dermato-Venereologica, 70(3), 251–253. https://doi.org/10.2340/0001555570251253
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