Abstract

<h3>Background:</h3> T-cell receptor (TCR) clonality is important for mycosis fungoides (MF) diagnosis. Routine clonality analysis is performed using a polymerase chain reaction (PCR) TCR-γ assay; yet with this method 10–50% of T-cell lymphomas escape detection. TCR-β gene rearrangement is an additional assay. Data about its efficacy is controversial. <h3>Objective:</h3> Evaluate the role of TCR-β assay in the diagnosis of early MF. <h3>Methods:</h3> A retrospective study of 61 skin biopsies, 20 from MF patients, 30 from patients suspected to have early MF, and 11 from patients with chronic inflammatory skin disease. <h3>Results:</h3> Monoclonality was detected in 16/20 (80%) MF cases; 15 (75%) with TCR-β and 12 (60%) with TCR-γ assay. Of the 30 suspected early MF cases, 14 demonstrated monoclonality, all of which with TCR-β and 5 with TCR-γ assay. None of the chronic inflammatory condition samples showed monoclonality. Therefore, TCR-β clonality assay was more sensitive in early MF than TCR-γ (83% vs. 43%, P=0.002). <h3>Limitations:</h3> A retrospective, relatively small study. <h3>Conclusion:</h3> TCR-β demonstrated a higher sensitivity rate compared with TCR-γ in early-stage MF. The combined use of the TCR-β and TCR-γ clonality tests can significantly improve the diagnosis rate of early-stage MF.

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