Cheong Jeanie L Y, Moorkamp Martina H
Royal Women's Hospital, Carlton, Vic 3053, Australia.
J Pediatr Hematol Oncol. 2007 Apr;29(4):262-4. doi: 10.1097/MPH.0b013e3180437e18.
Noonan syndrome (NS) is a multiple malformation syndrome where confirmation of diagnosis is difficult in the newborn. We report a case of a dysmorphic neonate who presented with bilateral chylous effusions and juvenile myelomonocytic leukemia where NS was confirmed by the presence of PTPN11 mutation. Juvenile myelomonocytic leukemia in NS is uncommon. The leukemia is usually self-limiting but lethal cases have been reported. Decisions regarding need for the treatment are unclear and further understanding of the genotype-phenotype relationships in PTPN11 mutations may help direct this.
努南综合征(NS)是一种多畸形综合征,新生儿确诊困难。我们报告一例畸形新生儿,其出现双侧乳糜性积液和青少年型骨髓单核细胞白血病,通过存在PTPN11突变确诊为NS。NS中的青少年型骨髓单核细胞白血病并不常见。这种白血病通常是自限性的,但也有致死病例的报道。关于是否需要治疗的决策尚不清楚,进一步了解PTPN11突变中的基因型-表型关系可能有助于指导这一决策。