Utility of CD30, Ki-67, and p53 in assisting with the diagnosis of mycosis fungoides with large cell transformation
Author:
Affiliation:
1. Department of Pathology; Stanford University; Stanford California
2. Department of Dermatology; Stanford University; Stanford California
3. Department of Dermatology; Palo Alto Medical Foundation; Palo Alto California
Publisher
Wiley
Subject
Dermatology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/cup.13375/fullpdf
Reference28 articles.
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2. Transformation of mycosis fungoides/Sezary syndrome: clinical characteristics and prognosis;Diamandidou;Blood,1998
3. Prognostic factors in transformed mycosis fungoides: a retrospective analysis of 100 cases;Benner;Blood,2012
4. Transformation of mycosis fungoides: clinicopathological and prognostic features of 45 cases. French Study Group of Cutaneous Lymphomas;Vergier;Blood,2000
5. Long-term outcome of 525 patients with mycosis fungoides and Sezary syndrome: clinical prognostic factors and risk for disease progression;Kim;Arch Dermatol,2003
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2. Intraindividual variability of CD30 expression in mycosis fungoides –implications for diagnostic evaluation and therapy;Histopathology;2022-05-04
3. PEG10 amplification at 7q21.3 potentiates large-cell transformation in cutaneous T-cell lymphoma;Blood;2022-01-27
4. Cutaneous Lymphomas;Handbook of Practical Immunohistochemistry;2022
5. Characteristics and outcomes of 727 patients with mycosis fungoides and Sézary syndrome from a Brazilian cohort;International Journal of Dermatology;2021-08-26
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