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伴有嗜酸性粒细胞增多和der(1;7)的骨髓增生异常综合征之前发生的多发性骨髓瘤

[Multiple myeloma preceding myelodysplastic syndrome with eosinophilia and der (1;7)].

作者信息

Matano S, Kobayashi K, Nakamura S, Yoshida T

机构信息

Department of Internal Medicine, Tonami General Hospital.

出版信息

Rinsho Ketsueki. 1994 Nov;35(11):1310-4.

PMID:7823398
Abstract

Multiple myeloma (IgG kappa + IgA kappa type, clinical stage IA) was diagnosed in a 82-year-old woman in January 1986. Chemotherapy (melphalan, prednisolone, vindesine, cyclophosphamide), caused prolonged myelosuppression. Therefore she was given other treatment. In October 1992, her peripheral blood examination demonstrated 2% blastic cells and 12% eosinophils. Bone marrow aspiration showed dysplastic features of trilineage blood cells with 4.8% myeloblasts. The karyotype of bone marrow cells from this patients was 47, XX, +der(1)t(1;7) (p11;p11), -7, +8. A diagnosis of therapy-related myelodysplastic syndrome (refractory anemia) was established. Eleven months after diagnosis of myelodysplastic syndrome, she is alive without leukemic transformation.

摘要

1986年1月,一名82岁女性被诊断为多发性骨髓瘤(IgG κ + IgA κ型,临床分期IA期)。化疗(美法仑、泼尼松龙、长春地辛、环磷酰胺)导致长期骨髓抑制。因此,她接受了其他治疗。1992年10月,她的外周血检查显示有2%的原始细胞和12%的嗜酸性粒细胞。骨髓穿刺显示三系血细胞发育异常,原始粒细胞占4.8%。该患者骨髓细胞的核型为47, XX, +der(1)t(1;7)(p11;p11), -7, +8。确诊为治疗相关的骨髓增生异常综合征(难治性贫血)。在诊断为骨髓增生异常综合征11个月后,她仍然存活,未发生白血病转化。

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