Hutter J J, Hecht F, Kaiser-McCaw B, Hays T, Baranko P, Cohen J, Durie B
Hematol Oncol. 1984 Jan-Mar;2(1):5-12. doi: 10.1002/hon.2900020103.
The hematologic manifestations and clinical course are described for six children and adolescents with bone marrow monosomy 7. One child with secondary acute myelogenous leukemia had monosomy 7 plus a marker chromosome; the remaining patients had marrow monosomy 7 as the only karyotypic abnormality. The hematologic abnormalities were diverse, but the majority of patients had a smoldering preleukemic or myeloproliferative phase. Leukemic blasts were either undifferentiated or demonstrated evidence of myeloid differentiation. All patients responded poorly to antileukemic therapy. Bone marrow monosomy 7 was observed in one patient with severe marrow hypoplasia. Antileukemic therapy in another patient with greater than 30 per cent marrow blasts was associated with the development of a bone marrow myeloproliferative disorder with persistence of the monosomy 7 karyotype. We speculate that monosomy 7 may be a specific marker for a pluripotent hematopoietic stem cell abnormality that is associated with either blastic leukemia or a myeloproliferative disorder.
描述了6例患有骨髓单体7的儿童和青少年的血液学表现及临床病程。1例继发性急性髓系白血病患儿除单体7外还有一条标记染色体;其余患者骨髓单体7是唯一的核型异常。血液学异常多种多样,但大多数患者有隐匿性白血病前期或骨髓增殖期。白血病原始细胞要么未分化,要么有髓系分化的证据。所有患者对抗白血病治疗反应不佳。1例严重骨髓发育不全患者观察到骨髓单体7。另1例骨髓原始细胞大于30%的患者接受抗白血病治疗后出现骨髓增殖性疾病,且单体7核型持续存在。我们推测单体7可能是一种多能造血干细胞异常的特异性标志物,与急性白血病或骨髓增殖性疾病有关。