Polymerase chain reaction based gene rearrangement studies in the diagnosis of follicular lymphoma - Performance in formaldehyde-fixed tissue and application in clinical problem cases

被引:17
作者
Miettinen, M
Lasota, J
机构
[1] Armed Forces Institute of Pathology, Department of Soft Tissue Pathology, Washington, DC
[2] Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, 14th Street and Alaska Avenue, N.W.
关键词
lymphoma; translocation; molecular genetics; PCR; gene rearrangement; differential diagnosis;
D O I
10.1016/S0344-0338(97)80089-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The diagnostic potential of PCR-based studies on the immunoglobulin heavy chain (IgH) gene rearrangements and the t(14;18) translocation was evaluated in a series of 30 benign and 46 malignant follicular lymphoid lesions including difficult problem cases using formaldehyde-fixed and paraffin-embedded (FFPE) tissue Clonal IgH gene rearrangement was documented by PCR in 38/46 follicular lymphomas using two alternative (FR3A and FR2A-based) primer systems; all benign hyperplasias showed a polyclonal pattern. The t(14;18) translocation was documented in 20/46 cases, including cases that did not show a clonal IgH gene amplification; a weak signal was seen in 6 benign hyperplasias probably related to the recently described rare non-neoplastic cells carrying the t(14;18) translocation. Of the translocations in follicular lymphomas, 18 involved the major breakpoint region (MBR) and two the minor cluster region (MCR). The diagnosis of follicular lymphoma could be reached with at least one marker in over 90% of the cases. With these tests we diagnosed an incidental follicular lymphoma in the axillary dissection for breast carcinoma, and confirmed benign nature of an extreme follicular hyperplasia with a 2200 g spleen. One diffuse large cleaved cell lymphoma with subsequent follicular small cleaved cell lymphoma was diagnosed to have a similar t(14;18) translocation showing a link between the two seemingly different lymphomas. Our results show the power of a panel of PCR-based IgH gene rearrangement and t(14;18) translocation studies in follicular lymphoid lesions in FFPE tissue. Because the t(14;18) translocation may occur in nonneoplastic lymphoid cells with a low frequency, the results should be quantitatively compared with the positive control to ensure that the positive signal is from the neoplastic clonal population and not from rare non-neoplastic cells carrying this translocation.
引用
收藏
页码:9 / 19
页数:11
相关论文
共 35 条
[21]  
NGAN BY, 1989, BLOOD, V73, P1759
[22]  
PEZZELLA F, 1989, LANCET, V1, P779
[23]  
PEZZELLA F, 1990, AM J PATHOL, V137, P225
[24]  
PICKER LJ, 1987, AM J PATHOL, V128, P181
[25]   IMPROVED PCR METHOD FOR DETECTING MONOCLONAL IMMUNOGLOBULIN HEAVY-CHAIN REARRANGEMENT IN B-CELL NEOPLASMS [J].
RAMASAMY, I ;
BRISCO, M ;
MORLEY, A .
JOURNAL OF CLINICAL PATHOLOGY, 1992, 45 (09) :770-775
[26]  
REED TJ, 1993, DIAGN MOL PATHOL, V2, P43
[27]  
SAID JW, 1993, APPL IMMUNOHISTO M M, V1, P108
[28]  
SEGAL GH, 1994, ARCH PATHOL LAB MED, V118, P791
[29]   OPTIMAL PRIMER SELECTION FOR CLONALITY ASSESSMENT BY POLYMERASE CHAIN-REACTION ANALYSIS .2. FOLLICULAR LYMPHOMAS [J].
SEGAL, GH ;
JORGENSEN, T ;
SCOTT, M ;
BRAYLAN, RC .
HUMAN PATHOLOGY, 1994, 25 (12) :1276-1282
[30]   PRIMERS FREQUENTLY USED FOR DETECTING THE T(14-18) MAJOR BREAKPOINT ALSO AMPLIFY EPSTEIN-BARR VIRAL-DNA [J].
SEGAL, GH ;
SCOTT, M ;
JORGENSEN, T ;
BRAYLAN, RC .
DIAGNOSTIC MOLECULAR PATHOLOGY, 1994, 3 (01) :15-21