Fischkoff S A, Testa J R, Schiffer C A
University of Maryland Cancer Center, Baltimore.
Leukemia. 1988 Jun;2(6):394-7.
We report a patient with acute eosinophilic leukemia and a translocation (10;11)(p14;q21). Clinically, the disease was characterized by extreme hypereosinophilia with most eosinophils being immature, pronounced marrow infiltration with abnormal eosinophil precursors, skin and lymphoid infiltration with leukemic eosinophils, and only a brief remission from chemotherapy. This is the second report of a patient with this cytogenetic/clinicopathological association. In our patient, t(10;11)(p14;q21) was the sole karyotypic abnormality seen in the bone marrow, both at diagnosis and relapse. Thus, acute eosinophilic leukemia with t(10;11)(p14;q21) appears to be a rare, new clinical/cytogenetic association. Because both patients with this translocation responded only briefly to chemotherapy, this chromosomal abnormality may confer a poor prognosis.
我们报告了1例患有急性嗜酸性粒细胞白血病且伴有(10;11)(p14;q21)易位的患者。临床上,该疾病的特征为极度嗜酸性粒细胞增多,大多数嗜酸性粒细胞不成熟,骨髓有明显浸润,伴有异常嗜酸性粒细胞前体,皮肤和淋巴组织有白血病性嗜酸性粒细胞浸润,且化疗后仅短暂缓解。这是关于这种细胞遗传学/临床病理关联患者的第二例报告。在我们的患者中,无论是在诊断时还是复发时,t(10;11)(p14;q21)都是骨髓中唯一可见的核型异常。因此,伴有t(10;11)(p14;q21)的急性嗜酸性粒细胞白血病似乎是一种罕见的新的临床/细胞遗传学关联。由于这两名患有这种易位的患者对化疗均仅短暂反应,这种染色体异常可能预示预后不良。