Chantrain Christophe F, Jijon Priscilla, De Raedt Thomas, Vermylen Christiane, Poirel Hélène A, Legius Eric, Brichard Bénédicte
Department of Pediatric Hematology-Oncology, St-Luc University Hospital, Catholic University of Louvain, Brussels, Belgium.
Pediatr Blood Cancer. 2007 Jan;48(1):101-4. doi: 10.1002/pbc.20527.
A 4-year-old girl with Noonan syndrome (NS) and constitutive PTPN11 mutation presented with stage 4 neuroblastoma and was treated by intensive chemotherapy. During the treatment, cytogenetic analysis revealed the development of a hyperdiploid clone with duplication of the germline PTPN11 mutation in a morphologically normal bone marrow. A few months later, the patient developed acute myelomonoblastic leukemia with an additional clonal deletion of 7q. Although, we cannot conclude whether there is an association between NS and neuroblastoma, this case suggests that duplication of germline PTPN11 mutations, potentially induced by chemotherapy, contributes to leukemogenesis in patients with NS.
一名患有努南综合征(NS)且存在组成型PTPN11突变的4岁女孩,患4期神经母细胞瘤,接受了强化化疗。治疗期间,细胞遗传学分析显示在形态学正常的骨髓中出现了一个超二倍体克隆,该克隆带有种系PTPN11突变的重复。几个月后,该患者发展为急性粒单核细胞白血病,伴有额外的7号染色体长臂克隆性缺失。虽然我们不能得出NS与神经母细胞瘤之间是否存在关联的结论,但该病例表明,化疗可能诱导的种系PTPN11突变重复,在NS患者的白血病发生过程中起作用。