A lymphohistiocytic variant of anaplastic large cell lymphoma with demonstration of the t(2;5)(p23;q35) chromosome translocation
Author:
Affiliation:
1. Pathologisches Institut,
2. Dermatologische Klinik und Poliklinik,
3. Department of Pathology, Beth Israel Hospital and Harvard Medical School, Boston, Mass., U.S.A.
4. Poliklinik für Innere Medizin, University of Würzburg, Würzburg, Germany,
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2141.1998.00531.x
Reference12 articles.
1. Detection of t(2;5)(p23;q35) translocation by reverse transcriptase polymerase chain reaction and in situ hybridization in CD30‐positive primary cutaneous lymphoma and lymphomatoid papulosis;Beylot‐Barry M.;American Journal of Pathology,1996
2. The t(2;5) chromosomal translocation is not a common feature of primary cutaneous CD30+ lymphoproliferative disorders: comparison with anaplastic large‐cell lymphoma of nodal origin;DeCoteau J.F.;Blood,1996
3. A Small-Cell-Predominant Variant of Primary Ki-1 (CD30)+ T-Cell Lymphoma
4. High incidence of the t(2;5)(p23;q35) translocation in anaplastic large cell lymphoma and its lack of detection in Hodgkin's disease: comparison of cytogenetic analysis, reverse transcriptase–polymerase chain reaction, and p‐80 immunostaining;Lamant L.;Blood,1996
5. The t(2;5)(p23;q35): a recurring chromosomal abnormality in Ki‐1‐positive anaplastic large cell lymphoma;Le Beau M.M.;Leukemia,1989
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