White J G, Thomas A
Department of Laboratory Medicine, Pathology and Pediatrics, University of Minnesota School of Medicine, Minneapolis, MN, USA.
Platelets. 2009 Feb;20(1):41-9. doi: 10.1080/09537100802406661.
The ultrastructural pathology of GATA-1, V205M and G208S macrothrombocytes was discussed in earlier investigations. This study has used the same technology to evaluate macrothrombocytes from a patient with the GATA-1, R216Q mutation. Some of the pathological features observed in macrothrombocytes from patients with the V205M and G208S variations including hypo- and agranular platelets, tubular inclusions and platelets within platelets, as well as platelets within platelets within platelets were identified. However, tubular membrane sheets in megakaryocytes and platelets of the V205M and G208S types and large groups of platelets attached to platelets to form megathrombocytes were not observed. The unique pathology of the megathrombocytes from this patient was the near absence of dense bodies in his giant cells. Storage Pool Deficiency, together with large platelets, defective adhesion and aggregation of his macrocytes under shear stress to vWF and collagen and defective clot retraction may contribute to the pathogenesis of his bleeding disorder.
早期研究讨论了GATA-1、V205M和G208S大血小板的超微结构病理学。本研究采用相同技术评估一名患有GATA-1 R216Q突变患者的大血小板。在V205M和G208S变异患者的大血小板中观察到的一些病理特征包括低颗粒和无颗粒血小板、管状内含物以及血小板内有血小板,还有血小板内血小板内有血小板。然而,未观察到V205M和G208S型巨核细胞和血小板中的管状膜片以及大量血小板附着形成巨大血小板。该患者大血小板的独特病理学表现是其巨细胞中几乎没有致密体。储存池缺陷,连同大血小板、其大血小板在剪切应力下对vWF和胶原蛋白的粘附和聚集缺陷以及凝块回缩缺陷,可能导致其出血性疾病的发病机制。