DETECTION OF CLONAL T-CELL RECEPTOR-GAMMA CHAIN GENE REARRANGEMENTS BY POLYMERASE-CHAIN-REACTION AND DENATURING GRADIENT GEL-ELECTROPHORESIS (PCR DGGE) IN ARCHIVAL SPECIMENS FROM PATIENTS WITH EARLY CUTANEOUS T-CELL LYMPHOMA - CORRELATION OF HISTOLOGIC-FINDINGS WITH PCR/DGGE/
J. Tok et al., DETECTION OF CLONAL T-CELL RECEPTOR-GAMMA CHAIN GENE REARRANGEMENTS BY POLYMERASE-CHAIN-REACTION AND DENATURING GRADIENT GEL-ELECTROPHORESIS (PCR DGGE) IN ARCHIVAL SPECIMENS FROM PATIENTS WITH EARLY CUTANEOUS T-CELL LYMPHOMA - CORRELATION OF HISTOLOGIC-FINDINGS WITH PCR/DGGE/, Journal of the American Academy of Dermatology, 38(3), 1998, pp. 453-460
Background: Early stages of cutaneous T-cell lymphoma (CTCL) may be di
fficult to distinguish from benign inflammatory dermatoses by routine
histologic examination. Objective: Our purpose was to determine whethe
r clonal rearrangements of the T-cell receptor (TCR) gamma gene by pol
ymerase chain reaction and denaturing gradient gel electrophoresis (PC
R/DGGE) could be detected in the early stages of CTCL and to correlate
these findings with conventional histopathology. Methods: A total of
39 specimens from 12 patients with CTCL were obtained. The slides were
evaluated independently by three dermatopathologists, and categorized
into three groups: nondiagnostic, suggestive of CTCL, and diagnostic
of CTCL. Of the 39 specimens, 33 were tested by PCR/DGGE by means of G
C-clamped primers for clonal rearrangement of the TCR gamma gene. Resu
lts: The histologic evaluation of the 12 cases showed a significant va
riation among the three dermatopathologists. The correlation of PCR/DG
GE with routine histology was as follows: Clonal TCR gamma gene rearra
ngements were demonstrated in 73% of the specimens nondiagnostic for C
TCL, 71% of those suggestive of CTCL, and 74% of those diagnostic of C
TCL. Conclusion: Clonal TCR gamma gene rearrangements may be detected
in patients with early CTCL, even when the histologic findings are not
unequivocally diagnostic. In patients with multiple biopsy specimens,
identical clones were demonstrated in all rearranged samples, indicat
ing the same neoplastic clone was present in the earliest stages of di
sease.