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The t(8;14)(q24.1;q32) and its variant translocations: A study of 34 cases.

作者信息

Angi Meenu, Kamath Vandana, Yuvarani S, Meena J, Sitaram Usha, Manipadam Marie Therese, Nair Sukesh, Ganapule Abhijeet, Fouzia N A, Abraham Aby, Viswabandya Auro, Poonkuzhali B, George Biju, Mathews Vikram, Srivastava Alok, Srivastava Vivi M

机构信息

Cytogenetics Unit, Christian Medical College & Hospital, Vellore, Tamil Nadu 632004, India.

Department of Hematology, Christian Medical College & Hospital, Vellore, Tamil Nadu, India.

出版信息

Hematol Oncol Stem Cell Ther. 2017 Sep;10(3):126-134. doi: 10.1016/j.hemonc.2017.03.002. Epub 2017 Mar 31.

DOI:10.1016/j.hemonc.2017.03.002
PMID:28390216
Abstract

BACKGROUND

The t(8;14)(q24.1;q32) and its variants - the t(2;8)(p12;q24.1) and t(8;22)(q24.1;q11.2) are associated with B-cell neoplasia and result in MYC/immunoglobulin (IG) gene rearrangement.

PATIENTS AND METHODS

We correlated the cytogenetic, molecular and clinico-pathological findings of patients with 8q24 translocations seen in the Department of Haematology, Christian Medical College, Vellore, from January 2003 to December 2015.

RESULTS

There were 34 patients with 8q24 translocations (31, ALL and three myeloma). The t(8;14) was seen in 25 patients, t(8;22) in seven and t(2;8) in two. The salient findings were as follows: 85% males; 79% adults, median age 37 years; L3 morphology in 61%; mature B immunophenotype in 77%; extra-medullary disease in 41%; additional abnormalities in 28 (85%), notably, structural abnormalities of chromosome 1q (41%) and 13q (9%) and monosomy 13 (15%); complex karyotypes in 68%. There were two double-hit lymphoma/leukemia, one with a t(14;18)(q32;q21) and the other with a t(3;14)(q27;q11.2), associated with nodal high grade B cell lymphoma and dermal leukemic infiltrates respectively. Only 13 samples were processed for DNA PCR and all these samples were positive for MYC-IgH (c-gamma type) rearrangement. Only in one patient, in addition to c-gamma, c-alpha rearrangement was also detected.

CONCLUSION

The frequency (1.7%) and distribution of these translocations in our series and the association with 1q and 13q abnormalities is similar to the literature. Trisomies 7 and 12 were seen in less than 10% of our patients.

摘要

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