Abstract
The CD30-postive lymphoproliferative disorders, including lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma, account for up to 30% of all cutaneous T-cell lymphomas (CTCLs) and are the second most common form of CTCLs after mycosis fungoides. Both conditions differ in their clinical presentations; however, they share the expression of the CD30 antigen as a common immunophenotypic hallmark. There is a wide spectrum of management options depending on factors such as extent of disease, staging and treatment tolerability. This Clinical Practice Statement is reflective of the current clinical practice in Australia.
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Bhabha, F. K., McCormack, C., Campbell, B. A., Lade, S., Buelens, O., Van Der Weyden, C., & Prince, H. M. (2023, May 1). CD30-positive lymphoproliferative disorders—An Australian Clinical Practice Statement from the Peter MacCallum Cancer Centre. Australasian Journal of Dermatology. John Wiley and Sons Inc. https://doi.org/10.1111/ajd.14016
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