The utility of PAX5 immunohistochemistry in the diagnosis of undifferentiated malignant neoplasms

被引:28
作者
Jensen, Kristin C.
Higgins, John P. T.
Montgomery, Kelli
Kaygusuz, Gulsah
van de Rijn, Matt
Natkunam, Yasodha
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Dept Pathol, Palo Alto, CA USA
[3] Ankara Univ, Sch Med, Dept Pathol, TR-06100 Ankara, Turkey
关键词
PAX5; B cell; non-Hodgkin lymphoma; Hodgkin lymphoma; undifferentiated neoplasm;
D O I
10.1038/modpathol.3800831
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
PAX5 is a B-cell transcription factor whose expression at the protein level is reliably detected by immunohistochemistry in routine biopsies. The purpose of this study was to investigate whether PAX5 immunohistochemistry has diagnostic benefit as a B-cell marker in the work-up of undifferentiated malignant neoplasms. Twenty-five cases previously diagnosed as undifferentiated malignant neoplasms were selected. In addition, 59 hematolymphoid and 884 non-hematolymphoid malignancies were studied such that the specificity of PAX5 immunohistochemistry could be addressed. Two of the 25 (8%) undifferentiated neoplasms showed diffuse staining for PAX5, which indicated a B-cell derivation for these neoplasms that was not appreciated at the time of initial diagnosis. PAX5 staining was detected in the vast majority of hematolymphoid tumors of B-cell derivation but only in 5 of 884 (less than 1%) non-hematolymphoid tumors. Our results further show that PAX5 may be the only detectable marker of B lineage in lymphomas that lack or show equivocal CD45RB and CD20 expression. We conclude that the addition of PAX5 to a panel of immunohistologic markers used in the interrogation of undifferentiated neoplasms is of diagnostic benefit. Its expression can also facilitate the diagnosis of classical and nodular lymphocyte-predominant Hodgkin lymphoma with atypical morphologic and immunohistologic features. Lastly, we have shown that the lack of its expression at the protein level in many epithelial and mesenchymal neoplasms renders PAX5 expression an extremely specific marker of the B lineage.
引用
收藏
页码:871 / 877
页数:7
相关论文
共 34 条
[1]   PAX-5 ENCODES THE TRANSCRIPTION FACTOR BSAP AND IS EXPRESSED IN LYMPHOCYTES-B, THE DEVELOPING CNS, AND ADULT TESTIS [J].
ADAMS, B ;
DORFLER, P ;
AGUZZI, A ;
KOZMIK, Z ;
URBANEK, P ;
MAURERFOGY, I ;
BUSSLINGER, M .
GENES & DEVELOPMENT, 1992, 6 (09) :1589-1607
[2]  
Adshead JM, 1999, BJU INT, V83, P1039
[3]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[4]   The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome [J].
Babjuk M. ;
Soukup V. ;
Mareš J. ;
Dušková J. ;
Sedláček Z. ;
Trková M. ;
Pecen L. ;
Dvořáček J. ;
Hanuš T. ;
Kočvara R. ;
Novák J. ;
Povýšil C. .
International Urology and Nephrology, 2002, 34 (4) :495-501
[5]  
BALZER BL, 2004, MODERN PATHOL, V17, pA89
[6]   Chromosomal translocations involving paired box transcription factors in human cancer [J].
Barr, FG .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (12) :1449-1461
[7]   The B-cell transcription factors BSAP, Oct-2, and BOB.1 and the pan-B-cell markers CD20, CD22, and CD79a are useful in the differential diagnosis of classic Hodgkin lymphoma [J].
Browne, P ;
Petrosyan, K ;
Hernandez, A ;
Chan, JA .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2003, 120 (05) :767-777
[8]  
Browne P., 2004, MODERN PATHOL, V17, p246A
[9]   B-cell specific activation protein encoded by the PAX-5 gene is commonly expressed in Merkel cell carcinoma and small cell carcinomas [J].
Dong, HY ;
Liu, W ;
Cohen, P ;
Mahle, CE ;
Zhang, WS .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (05) :687-692
[10]  
GERARD M, 1995, CR ACAD SCI III-VIE, V318, P57