Primary cutaneous T-cell lymphomas other than mycosis fungoides and Sézary syndrome. Part I: Clinical and histologic features and diagnosis.

CD30(+) lymphoproliferative disorders Sézary syndrome T-cell lymphoma adult T-cell leukemia adult T-cell lymphoma angioimmunoblastic T-cell lymphoma cutaneous T-cell lymphoma cytotoxic primary cutaneous anaplastic large cell lymphoma extranodal NK/T-cell lymphoma lymphomatoid papulosis mycosis fungoides nasal type not otherwise specified peripheral T-cell lymphoma primary cutaneous CD4(+) small/medium T-cell lymphoproliferative disorder primary cutaneous CD8(+) aggressive epidermotropic cytotoxic T-cell lymphoma primary cutaneous acral CD8(+) T-cell lymphoma primary cutaneous gamma-delta T-cell lymphoma subcutaneous panniculitis-like T-cell lymphoma

Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
11 2021
Historique:
received: 01 02 2021
revised: 12 04 2021
accepted: 26 04 2021
pubmed: 4 5 2021
medline: 19 3 2022
entrez: 3 5 2021
Statut: ppublish

Résumé

Primary cutaneous T-cell lymphomas (CTCLs) are defined as lymphomas with a T-cell phenotype that present in the skin without evidence of systemic or extracutaneous disease at initial presentation. CTCLs other than mycosis fungoides and Sézary syndrome (SS) account for approximately one third of CTCLs and encompass a heterogenous group of non-Hodgkin lymphomas, ranging from indolent lymphoproliferative disorders to aggressive malignancies with a poor prognosis. The spectrum of CTCLs continues to broaden as new provisional entities are classified. Given the morphologic and histologic overlap among CTCLs and other diagnoses, a thorough clinical history, physical evaluation, and clinicopathologic correlation are essential in the work up and diagnosis of these rare entities. This article will summarize the epidemiologic, clinical, pathologic, and diagnostic features of CTCLs other than mycosis fungoides and SS.

Identifiants

pubmed: 33940098
pii: S0190-9622(21)00926-9
doi: 10.1016/j.jaad.2021.04.080
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1073-1090

Informations de copyright

Copyright © 2021 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest Dr Noor is on the Advisory Board for Kyowa Kirin. Dr Horowitz is a consultant for Janssen, Kura Oncology, Myeloid Therapeutics, Vividion Therapeutics, and C4 Therapeutics; a Principal Investigator for Daiichi Sankyo, Portola Pharmaceuticals, Forty Seven Inc, Trillium Therapeutics, and Aileron; and a Principal Investigator and consultant for Kyowa Kirin, Celgene, Seattle Genetics, Verastem, Takeda, and ADC Therapeutics. Dr Moskowitz is a consultant for Imbrium Therapeutics LP; a Principal Investigator for Miragen, Incyte, Bristol-Myers Squibb; and a Principal Investigator and consultant for Merck and Seattle Genetics. Authors Stoll and Oh and Drs Pulitzer, Willner, and Myskowski have no conflicts of interests to declare.

Auteurs

Joseph R Stoll (JR)

Memorial Sloan Kettering Cancer Center, New York, New York.

Jonathan Willner (J)

Memorial Sloan Kettering Cancer Center, New York, New York.

Yuna Oh (Y)

Memorial Sloan Kettering Cancer Center, New York, New York.

Melissa Pulitzer (M)

Memorial Sloan Kettering Cancer Center, New York, New York.

Alison Moskowitz (A)

Memorial Sloan Kettering Cancer Center, New York, New York.

Steven Horwitz (S)

Memorial Sloan Kettering Cancer Center, New York, New York.

Patricia Myskowski (P)

Memorial Sloan Kettering Cancer Center, New York, New York.

Sarah J Noor (SJ)

Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: noors2@mskcc.org.

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Classifications MeSH