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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: Am J Surg Pathol. 2018 Feb;42(2):269–276. doi: 10.1097/PAS.0000000000000982

Table 1.

Clinical and pathological features of adult B-ALL/LBL with isolated MYC translocation

Prior and current reports Age Sex Initial presentation Treatment and Course FISH(%)
Cytogenetics
BCL2 R
BCL6 R
CD10 CD19 CD20 BCL-6 CD34 TdT sIg EBER
Komrokji R, et al 45 M B symptoms, splenomegaly Hyper-CVAD alternating with high dose MTX/ARA-C t(8,14)(q24,q32), +i(1)(q10) NT + + + NT NT
Shiratori S, et al 64 F Choroid and skin involvement by B-LBL Achieved CR after R-CHOP × 6; relapsed on skin 2 years later, achieved CR after radiation therapy; a further 2 years later, skin and choriod relapse as in initial stage t(8;14)(q24;q32); positive IGH and TCR gene rearrangement + + + NT + NT NT
Slavutsky I, et al 20 F B symptoms, hepatomegaly, large retroperitoneal lymphadenopathy, and nephromegaly n/a t(8;22)(q24;q 11); hyperploid NT + + NT NT NT NT
Li Y, et al
Case 1 70 M Diffuse lymphadnopathy, splenomegaly, PB and BM involvement Hyper-CVAD and intrathecal methotrexate. Expired during the second cycle of chemotherapy MYC/IGH (55%); 5q deleion (7/20) metaphases + + + +
Case 2 56 M Diffuse lymphadenopathy, hepatosplenomegaly, PB and BM involvment High-risk ALL protocol (8707) with initial remission, but with progression two months after treatment. MYC/IGH (60%) + + −/+
Case 3 44 M Bulky intrabdominal lymphadenopathy, negative BM Hyper-CVAD with partial remission, pending stem cell transplant MYC/IGH (63%) + NT + + NT

Abbreviations: NT, not tested; PB, peripheral blood; BM, bone marrow