Institute of Pathology, Hannover Medical School, Hannover, Germany.
Division of Pediatric Hematology and Oncology, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
Pediatr Blood Cancer. 2018 Jul;65(7):e27048. doi: 10.1002/pbc.27048. Epub 2018 Apr 18.
Pediatric fibrotic myelodysplastic syndromes (ped-MDS-MF) and pediatric primary myelofibrosis (ped-PMF) are rare, and the molecular changes which mediate fibrosis have never been investigated. Histology and gene expression profile of 119 fibrosis/angiogenesis/inflammation/megakaryopoiesis-related factors in bone marrow biopsies were performed (two ped-MDS-MF and one ped-PMF). In one progressive ped-MDS, comparison of MF grade 0 (no myelofibrosis) and MF grade 2 (dense network of reticulin fibres) after 4 months showed that expression of fibrosis-related transcripts increased and dysplastic megakaryocytes formed a dense net of CD42b proplatelets. These changes were not observed in another ped-MDS-MF, whereas ped-PMF showed a similar proplatelet pattern. These findings indicate that fibrotic changes in ped-MDS may involve proplatelet-related and unrelated pathways.
儿科纤维性骨髓增生异常综合征(ped-MDS-MF)和儿科原发性骨髓纤维化(ped-PMF)较为罕见,介导纤维化的分子变化从未被研究过。对 119 例骨髓活检中与纤维化、血管生成、炎症和巨核细胞生成相关的因素进行了组织学和基因表达谱分析(2 例 ped-MDS-MF 和 1 例 ped-PMF)。在一例进行性 ped-MDS 中,比较了 MF 0 级(无骨髓纤维化)和 MF 2 级(网状纤维密集)4 个月后的结果,发现纤维化相关转录物的表达增加,并且发育异常的巨核细胞形成了密集的 CD42b 血小板网络。这些变化在另一个 ped-MDS-MF 中没有观察到,而 ped-PMF 则显示出类似的血小板网络形成模式。这些发现表明 ped-MDS 中的纤维化变化可能涉及与血小板相关和不相关的途径。