Polymerase chain reaction-based detection of B-cell clonality in the fine needle aspiration biopsy of a thyroid mucosa-associated lymphoid tissue (MALT) lymphoma

被引:25
作者
Lovchik, J [1 ]
Lane, MA [1 ]
Clark, DP [1 ]
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT PATHOL,DIV CYTOPATHOL,BALTIMORE,MD 21205
关键词
polymerase chain reaction; monoclonality; fine needle aspiration; MALT lymphoma; thyroid;
D O I
10.1016/S0046-8177(97)90017-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Although it is possible to diagnose primary high-grade thyroid lymphoma from a fine needle aspiration (FNA) biopsy, the distinction of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) from lymphocytic thyroiditis is sometimes problematic, Definitive diagnosis of lymphoma on cytologic specimens may be facilitated by the documentation of a clonal lymphoid proliferation within the specimen by flow cytometric immunophenotyping or immunocytochemistry, Recently, molecular techniques have also been developed to detect clonal lymphoid proliferation based on immunoglobulin (Ig) or T-cell receptor gene rearrangement, We have used a polymerase chain reaction (PCR)-based assay for Ig heavy chain gene arrangement to identify a clonal population of lymphocytes within the thyroid FNA specimen from a low-grade thyroid MALT lymphoma. Using this assay, we identified no distinct clonal population in five cytologic specimens of lymphocytic thyroiditis, Therefore, this PCR-based clonality assay represents a potentially useful adjunct to the cytologic diagnosis of thyroid lymphoma. (C) 1997 by W.B. Saunders Company.
引用
收藏
页码:989 / 992
页数:4
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