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ÇǺΠT¼¼Æ÷ Áõ½Ä¼º º´º¯ÀÇ Å¬·Ð¼º È®ÀÎ Molecular Diagnosis of Cutaneous T Cell Lymphoproliferative Diseases

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¹ÚÁö¿µ ( Park Ji-Young ) 
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À̸íÈÆ ( Lee Myung-Hoon ) 
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°ûÀº°æ ( Kwak Eun-Kyung ) 
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±èµ¿ÀÚ ( Kim Dong-Ja ) 
°æºÏ´ëÇб³º´¿ø Çغκ´¸®°ú
¹ÚÅÂÀΠ( Park Tae-In ) 
°æºÏ´ëÇб³º´¿ø Çغκ´¸®°ú
¹èÇÑÀÍ ( Bae Han-Ik ) 
°æºÏ´ëÇб³º´¿ø Çغκ´¸®°ú

Abstract


It is often problematic to diagnose T-cell lymphoproliferative disorders of the skin because of the difficulty in establishing clonality in paraffin-embedded tissue. We used polymerase chain reaction single strand conformational polymorphism (PCR-SSCP) and heteroduplex analysis in paraffin embedded tissue to detect clonal rearrangement of T-cell receptor ¥ã (TCR¥ã) gene in 17 T-cell lymphoproliferative disorders and 6 atypical lymphoproliferative diseases. We used polymerase chain reaction to detect TCR¥â gene rearrangement in 8 of 17 cases which did not show TCR¥ã gene rearrangement. Jurkat cell lines were used as monoclonal controls. DNA was extracted from 5 biopsies of T-cell lymphomas, 10 biopsies of mycosis fungoides, 2 biopsies of lymphomatoid papulosis, and 6 biopsies of atypical lymphoproliferative lesions. We detected monoclonality in 5 of 5 T-cell lymphoma cases, 2 of 2 lymphomatoid papulosis cases, 6 of 10 mycosis fungoides cases, and 2 of 6 atypical lymphoproliferative disease cases. We conclude that nonradioactive PCR-SSCP for TCR gene rearrangement analysis is a useful adjunct to routine histological and immunophenotypic methods in the diagnosis of cutaneous T cell lymphoproliferative disorders in paraffin embedded tissue.

Å°¿öµå

Polymerase chain reaction;Single strand conformational polymorphism;Heteroduplex;T-cell receptor;Cutaneous T-cell lymphoproliferative diseases

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