Follicular lymphoma grade 3B is a distinct neoplasm according to cytogenetic and immunohistochemical profiles

According to the current World Health Organization Classification of Lymphoid Tumours, follicular lymphoma is subclassified into three grades according to the number of centroblasts. Follicular lymphoma grade 3 can be further divided into types A and B. Almost all available genetic data on grade 3B...

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Veröffentlicht in:Haematologica (Roma) 2011-09, Vol.96 (9), p.1327-1334
Hauptverfasser: HORN, Heike, SCHMELTER, Christopher, OTT, German, LEICH, Ellen, SALAVERRIA, Itziar, KATZENBERGER, Tiemo, MICHAELA OTT, M, KALLA, Jörg, ROMERO, Monica, SIEBERT, Reiner, ROSENWALD, Andreas
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Sprache:eng
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Zusammenfassung:According to the current World Health Organization Classification of Lymphoid Tumours, follicular lymphoma is subclassified into three grades according to the number of centroblasts. Follicular lymphoma grade 3 can be further divided into types A and B. Almost all available genetic data on grade 3B follicular lymphomas have been generated from tumors with an additional diffuse large B-cell lymphoma component. The purely follicular type of follicular lymphoma grade 3B is a rare neoplasm. We performed a detailed immunohistochemical (CD10, IRF4/MUM1, BCL2, Ig light chains) and genetic (translocations of BCL2, BCL6, MYC, IRF4) characterization of the largest series of purely follicular cases of grade 3B follicular lymphoma available to date, comprising 23 tumor samples. We also included 25 typical grade 1 or 2 follicular lymphomas, 9 follicular lymphomas with large centrocytes and/or high proliferation indices (FL/LCC), 12 cases of follicular lymphoma grade 3A, 16 cases of diffuse large B-cell lymphoma/follicular lymphoma grade 3B and 15 follicular lymphomas in which a straightforward distinction between grades 3A and 3B was not possible. Translocations affecting BCL2 and BCL6 genes are rare in grade 3B follicular lymphomas (2/23, 9% and 4/23, 17%) when compared with grade 1 or 2 follicular lymphomas (22/25, 88%, P
ISSN:0390-6078
1592-8721
DOI:10.3324/haematol.2011.042531