Behrendt H, Charrin C, Gibbons B, Harrison C J, Hawkins J M, Heerema N A, Horschler-Bötel B, Huret J L, Laï J L, Lampert F
Institute of Human Genetics, Academic Medical Center, Amsterdam, The Netherlands.
Leukemia. 1995 Jan;9(1):102-6.
Fourteen cases of dic(9;12)(p11-13;p11-12) in early B-lineage acute lymphoblastic leukemia (ALL) and other hematological malignancies are reported with a review of the literature. Altogether 36 cases were collected for analysis: ALL at diagnosis (31 cases) or in relapse (one case), chronic myeloid leukemia in lymphoid blast crisis (two cases), T-cell lymphoblastic lymphoma (one case) and T-cell non-Hodgkin's lymphoma (one case). We report the first cases of dic(9;12) with a T-cell phenotype. Dic(9;12) occurs predominantly in B-progenitor ALL of childhood and young adults (age range, 1-47 years, median 12 years) but not of infancy. One or more adverse clinical features, age > 10 years, WBC > 100 x 10(9)/l, pre-B immunophenotype, platelets < 100 x 10(9)/l, were found in over 90% of cases. Additional structural chromosomal changes or trisomy 8 were frequently present. Nevertheless with a median follow-up of 5 years, 29/31 cases (94%) remain in first remission conferring an excellent prognosis to this leukemia. Additional cases are being sought to confirm the prognostic value of this cytogenetic aberration in various hematological malignancies.
本文报告了14例早期B系急性淋巴细胞白血病(ALL)及其他血液系统恶性肿瘤中发生的dic(9;12)(p11 - 13;p11 - 12),并对文献进行了综述。共收集了36例病例进行分析:诊断时的ALL(31例)或复发时的ALL(1例)、淋巴细胞母细胞危象期的慢性髓性白血病(2例)、T细胞淋巴母细胞淋巴瘤(1例)和T细胞非霍奇金淋巴瘤(1例)。我们报告了首例具有T细胞表型的dic(9;12)。Dic(9;12)主要发生在儿童和年轻成人(年龄范围1 - 47岁,中位年龄12岁)的B祖细胞ALL中,婴儿期则未发生。超过90%的病例具有一个或多个不良临床特征,年龄>10岁、白细胞>100×10⁹/L、前B免疫表型、血小板<100×10⁹/L。常伴有其他染色体结构改变或8号染色体三体。然而,中位随访5年时,31例中有29例(94%)仍处于首次缓解期,提示该白血病预后良好。正在寻找更多病例以证实这种细胞遗传学异常在各种血液系统恶性肿瘤中的预后价值。