Scheurlen W, Borkhardt A, Ritterbach J, Huppertz H I
Department of Pediatrics, University of Würzburg, Germany.
Leukemia. 1994 Aug;8(8):1435-8.
We report the case of a 14-month-old boy with myelodysplastic syndrome (refractory anemia with blast excess) and bone marrow monosomy 7. Within 2 years after presentation hematological remission gradually occurred without any chemotherapy. After the patient had received three transfusions within the first 4 months, red cell production normalized. However it took 18 more months for neutropenia to resolve. The patient is well 34 months after the first presentation. Molecular analysis of the bone marrow blasts showed no mutations of the ras genes or of the FLR-exon of the NF-1 gene. To our knowledge this is the first report of monosomy 7 syndrome with spontaneous hematological remission.
我们报告了一例14个月大的男孩,患有骨髓增生异常综合征(伴原始细胞增多的难治性贫血)及骨髓7号染色体单体。就诊后2年内,未进行任何化疗,血液学缓解逐渐出现。在最初4个月内患者接受了3次输血后,红细胞生成恢复正常。然而,中性粒细胞减少症又持续了18个月才得以缓解。首次就诊34个月后,患者情况良好。对骨髓原始细胞的分子分析显示,ras基因或NF-1基因的FLR外显子均无突变。据我们所知,这是7号染色体单体综合征自发血液学缓解的首例报告。