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Eur J Dermatol ; 30(1): 12-15, 2020 Feb 01.
Article in English | MEDLINE | ID: mdl-32250251

ABSTRACT

BACKGROUND: Early and precise diagnosis of cutaneous T-cell lymphomas (CTCL) is challenging. Currently, polymerase chain reaction (PCR)-based clonality assessment of the T-cell receptor (TCR) is a helpful tool for this diagnosis. OBJECTIVES: In this retrospective study, we aimed to assess the sensitivity and specificity of this method for the diagnosis of CTCL. MATERIALS AND METHODS: Monoclonal rearrangement of the TCR was investigated retrospectively by PCR-based clonality assessment based on 292 DNA samples from skin biopsies of patients with a suspicion of CTCL. Algorithms were based on different ratios (three or five-fold difference) between the dominant PCR peak and the third highest PCR peak. RESULTS: A PCR peak five-fold higher than the third highest PCR peak demonstrated significantly greater specificity (83.7% versus 76.4%) but lower sensitivity (59.8% versus 68.6%) compared to a cut-off of three-fold higher. CONCLUSION: Our results confirm the diagnostic value of TCR clonality analysis which may be used to define the ideal cut-off in order to optimize sensitivity and specificity.


Subject(s)
DNA/analysis , Lymphoma, T-Cell, Cutaneous/diagnosis , Receptors, Antigen, T-Cell/genetics , Skin Neoplasms/diagnosis , Aged , Algorithms , Biopsy , Female , Humans , Lymphoma, T-Cell, Cutaneous/pathology , Male , Middle Aged , Polymerase Chain Reaction , Retrospective Studies , Sensitivity and Specificity , Skin/pathology , Skin Neoplasms/pathology
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