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Assessing T-cell receptor clonality by next-generation sequencing in atypical cutaneous lymphoid infiltrates and cutaneous T-cell lymphoma: A scoping review.
Shinohara, Michi M; Rieger, Kerri E; Sundram, Uma; Fung, Maxwell A; Hristov, Alexandra C.
Afiliação
  • Shinohara MM; Department of Dermatology, University of Washington, Seattle, Washington, USA.
  • Rieger KE; Department of Pathology and Laboratory Medicine, University of Washington, Seattle, Washington, USA.
  • Sundram U; Department of Dermatology, Stanford University School of Medicine, Palo Alto, California, USA.
  • Fung MA; Department of Pathology, Stanford University School of Medicine, Palo Alto, California, USA.
  • Hristov AC; Department of Pathology, Oakland University William Beaumont School of Medicine and Beaumont Health Systems, Royal Oak, Michigan, USA.
J Cutan Pathol ; 2024 Jul 18.
Article em En | MEDLINE | ID: mdl-39021266
ABSTRACT
The diagnosis of cutaneous T-cell lymphoma (CTCL) remains challenging. Demonstration of a clonal T-cell population using T-cell receptor (TCR) gene rearrangement studies by next-generation sequencing (NGS) has been explored in several studies. This review summarizes the current literature on NGS-based sequencing methods for the assessment of TCR clonality in the evaluation of atypical cutaneous lymphoid infiltrates and CTCL on behalf of the American Society of Dermatopathology Appropriate Use Criteria Committee (lymphoproliferative subgroup). PubMed was searched for relevant articles, including CTCL and NGS, for clonality from 1967 to 2022. Thirteen studies were included in the analysis. The skin was the most commonly assayed compartment with TCR NGS. Sensitivity for TCR NGS in the skin ranged between 69% and 100%, compared to 44%-72% for polymerase chain reaction (PCR)-capillary electrophoresis. Specificity for TCR NGS in the skin ranged from 86% to 100%, compared to 77%-88% for PCR capillary electrophoresis. TCR NGS was also reported to have potential prognostic value in CTCL and can also be used to detect relapse and/or minimal residual disease after treatment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article