Departments of Paediatrics.
Division of Haematology/Oncology, The Hospital for Sick Children.
J Pediatr Hematol Oncol. 2023 Apr 1;45(3):e401-e405. doi: 10.1097/MPH.0000000000002492. Epub 2022 Jun 3.
Juvenile myelomonocytic leukemia (JMML) is a rare, aggressive pediatric disorder characterized by pathologic myeloproliferation because of alterations in RAS pathway genes. NRAS -mutated JMML encompasses a broad range of clinical severity. Herein we describe 4 unique cases of NRAS -mutated JMML and JMML-like myeloproliferation, 2 with somatic mutations and 2 with germline mutations. These cases illustrate the diverse clinical and hematologic presentation of this subtype of JMML, including a very unusual example presenting with Auer rods. Lastly, this is the first report of patients with phenotypic Costello syndrome presenting with JMML-like myeloproliferation, highlighting an important clinical phenomenon that has not been previously described.
儿童早发性骨髓单核细胞白血病(JMML)是一种罕见的侵袭性儿科疾病,其特征为 RAS 通路基因改变导致病理性骨髓增生。NRAS 突变型 JMML 具有广泛的临床严重程度。本文描述了 4 例独特的NRAS 突变型 JMML 和 JMML 样骨髓增生病例,其中 2 例存在体细胞突变,2 例存在种系突变。这些病例说明了该亚型 JMML 的不同临床表现和血液学表现,包括一例非常罕见的表现为 Auer 小体的病例。最后,这是首例表型 Costello 综合征患者出现 JMML 样骨髓增生的报告,强调了一种以前未描述的重要临床现象。