Intertriginous mycosis fungoides with T follicular helper cell phenotype progressing to Sézary syndrome.
- Resource Type
- Report
- Authors
- Amir Ali A; Division of Dermatology, Department of Medicine, University of Calgary, Calgary, AB, Canada.; Shameli A; Division of Hematology, Alberta Precision Laboratories, South Zone and Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.; Zhang C; Division of Dermatology, Department of Medicine, University of Calgary, Calgary, AB, Canada.; Gniadecki R; Division of Dermatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.; Street L; Division of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.; Hardin J; Division of Dermatology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
- Source
- Publisher: Oxford University Press Country of Publication: England NLM ID: 7606847 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2230 (Electronic) Linking ISSN: 03076938 NLM ISO Abbreviation: Clin Exp Dermatol Subsets: MEDLINE
- Subject
- Language
- English
This case report highlights the challenges in diagnosis and therapeutic options for an individual who initially presented with intertriginous mycosis fungoides with a T follicular helper cell phenotype, which later evolved to Sézary syndrome.
(© 2021 British Association of Dermatologists.)