Slayton William B, Patel Milin, Sola-Visner Martha, Harris Neil, Rivers Angela, Montgomery Robert R, Friedman Kenneth D
Department of Pediatrics, Drexel University, Philadelphia, PA, USA.
J Pediatr Hematol Oncol. 2008 Sep;30(9):708-11. doi: 10.1097/MPH.0b013e31817541cd.
We report a child with thrombocytopenia since birth, circulating platelet agglutinates, and a tendency to bleed. A bone marrow aspirate revealed large platelet clumps within the bone marrow and megakaryocyte nuclei surrounded by halos of clumped platelets. Laboratory evaluation revealed type 2B von Willebrand disease. Gene sequencing revealed a G to C mutation at base 3923 of the VWF gene. This mutation was previously described in a family with circulating platelet clumps and abnormal megakaryopoiesis with release of clumped platelets in culture. This same mutation was previously described in a family with circulating platelet aggregates and abnormalities of platelet release from megakaryocytes in vitro. Presence of megakaryocytes with halos of clumped platelets in our patient suggests that platelet agglutinate occurs in the bone marrow in some type 2B von Willebrand disease patients.
我们报告了一名自出生以来就患有血小板减少症、循环血小板凝集且有出血倾向的儿童。骨髓穿刺显示骨髓内有大量血小板团块以及被聚集血小板晕环绕的巨核细胞核。实验室评估显示为2B型血管性血友病。基因测序显示血管性血友病因子(VWF)基因第3923位碱基由G突变为C。该突变先前在一个有循环血小板团块且巨核细胞生成异常、培养中释放聚集血小板的家族中被描述过。同样的突变先前也在一个有循环血小板聚集体且体外巨核细胞血小板释放异常的家族中被描述过。我们患者中出现有聚集血小板晕的巨核细胞提示,在一些2B型血管性血友病患者中血小板凝集发生在骨髓中。