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Mycosis fungoides and Sézary syndrome: focus on the current treatment scenario
Author(s) -
José Antônio Sanches,
Jade CuryMartins,
Rodrigo Martins Abreu,
Denis Miyashiro,
Juliana Pereira
Publication year - 2021
Publication title -
anais brasileiros de dermatologia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 44
eISSN - 1806-4841
pISSN - 0365-0596
DOI - 10.1016/j.abd.2020.12.007
Subject(s) - mycosis fungoides , medicine , dermatology , cutaneous t cell lymphoma , lymphoma , bexarotene , stage (stratigraphy) , disease , radiation therapy , cutaneous lymphoma , peripheral t cell lymphoma , pathology , immunology , t cell , immune system , biology , paleontology , biochemistry , nuclear receptor , transcription factor , gene
Cutaneous T-cell lymphomas are a heterogeneous group of lymphoproliferative disorders, characterized by infiltration of the skin by mature malignant T cells. Mycosis fungoides is the most common form of cutaneous T-cell lymphoma, accounting for more than 60% of cases. Mycosis fungoides in the early-stage is generally an indolent disease, progressing slowly from some patches or plaques to more widespread skin involvement. However, 20% to 25% of patients progress to advanced stages, with the development of skin tumors, extracutaneous spread and poor prognosis. Treatment modalities can be divided into two groups: skin-directed therapies and systemic therapies. Therapies targeting the skin include topical agents, phototherapy and radiotherapy. Systemic therapies include biological response modifiers, immunotherapies and chemotherapeutic agents. For early-stage mycosis fungoides, skin-directed therapies are preferred, to control the disease, improve symptoms and quality of life. When refractory or in advanced-stage disease, systemic treatment is necessary. In this article, the authors present a compilation of current treatment options for mycosis fungoides and Sézary syndrome.

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