Sasaki Takuya, Yasuda Tsutomu, Abe Daijiro, Miyano Ryoji, Kainaga Mitsuhiro, Tomura Nagatsuki, Kitamura Mizuki, Nakayama Takahiro, Imafuku Ichiro
Department of Neurology, Yokohama Rosai Hospital, Yokohama, Kanagawa, Japan.
Department of Neurology, Yokohama Rosai Hospital, Yokohama, Kanagawa, Japan.
J Stroke Cerebrovasc Dis. 2019 Mar;28(3):789-791. doi: 10.1016/j.jstrokecerebrovasdis.2018.11.026. Epub 2018 Dec 13.
Although it was suggested that idiopathic thromobocytopenic purpura (ITP) can be a paradoxical cause of cerebral infarction, previous reports indicate that cerebral infarction associated with ITP occurs when thrombocytopenia is already evident at the onset of cerebral infarction.
We report a case of multiple cerebral infarction that preceded acute exacerbation of ITP. An 80-year-old woman with a history of ITP presented with tetraplegia, and brain magnetic resonance imaging revealed multiple infarction in bilateral cerebral and cerebellar hemispheres. For ITP, she was treated with oral prednisolone and subcutaneous injection of thrombopoietin receptor agonists. Her platelet count was within the normal range at the onset of cerebral infarction. Medical work-up did not reveal the obvious causes of her multiple cerebral infarction. On day 10 of hospitalization, she showed melena and oral hemorrhage and her platelet count markedly decreased. Her platelet-associated IgG level was elevated and a diagnosis of acute exacerbation of ITP was made. She was treated with intravenous immunoglobulin and her platelet count increased moderately. However, her neurological symptoms and cerebral infarction on magnetic resonance imaging deteriorated accompanied by hemorrhagic transformation. Finally, she died of respiratory failure.
Our case suggests that thrombophilia accompanied by ITP can precede actual exacerbation of ITP and we have to consider ITP as a possible cause of multiple cerebral infarction, even when the platelet count is within the normal range at the onset of cerebral infarction.
尽管有观点认为特发性血小板减少性紫癜(ITP)可能是脑梗死的反常病因,但既往报道表明,与ITP相关的脑梗死发生于脑梗死起病时血小板减少已很明显的情况下。
我们报告1例在ITP急性加重之前发生多发性脑梗死的病例。一名有ITP病史的80岁女性出现四肢瘫痪,脑磁共振成像显示双侧大脑半球和小脑半球多发梗死灶。对于ITP,她接受了口服泼尼松龙和皮下注射血小板生成素受体激动剂治疗。在脑梗死起病时,她的血小板计数在正常范围内。医学检查未发现其多发性脑梗死的明显病因。住院第10天,她出现黑便和口腔出血,血小板计数显著下降。她的血小板相关IgG水平升高,诊断为ITP急性加重。她接受了静脉注射免疫球蛋白治疗,血小板计数中度升高。然而,她的神经症状以及磁共振成像显示的脑梗死恶化,并伴有出血性转化。最终,她死于呼吸衰竭。
我们的病例提示,伴有ITP的血栓形成倾向可能先于ITP的实际加重,即使在脑梗死起病时血小板计数在正常范围内,我们也必须将ITP视为多发性脑梗死的可能病因。