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48岁男性,突发右侧肢体无力。

48 year old male with sudden onset of right sided weakness.

作者信息

Easton Alexander

机构信息

Department of Laboratory Medicine and Pathology, Walter C Mackenzie Health Sciences Centre, Edmonton, Canada.

出版信息

Brain Pathol. 2006 Apr;16(2):181-2, 187. doi: 10.1111/j.1750-3639.2006.00003_1.x.

Abstract

This 48 year-old male presented with sudden right sided weakness and hypertension, and on CT was found to have a deep left hemispheric intracerebral hematoma. There were accompanying bilateral hypointensities in the occipital lobes, unchanged 1 day later, when expansion of the hematoma and uncal herniation resulted in death. The past medical history included liver transplantation followed by long term cyclosporin, features of thrombotic thrombocytopenic purpura (TTP) attributed to cyclosporin, type 1 diabetes mellitus and acute renal failure attributed to diabetic nephropathy. There was a 2-month history of hypertension poorly responsive to therapy. The occipital lobes at autopsy showed focal cortical hemorrhages with bilateral discoloration of white matter sparing subcortical zones. Microscopy showed white matter pallor with parenchymal cysts, enlarged perivascular spaces and focal acute hemorrhages consistent with edema secondary to acute hypertension. Cortical hemorrhages were associated with intravascular thrombi and fibrin exudates, as well as an accompanying microinfarct, attributed to TTP. The occipital pathology reflects the posterior leukoencephalopathy syndrome (PLS) combined with cortical lesions of TTP. PLS is usually diagnosed radiologically by occipital hypointensities, and is reversible, so that autopsy pathology is rarely examined. TTP may predispose to the development of the PLS in certain cases.

摘要

这位48岁男性患者突发右侧肢体无力和高血压,CT检查发现左侧大脑半球深部脑出血。枕叶出现双侧低密度影,1天后无变化,之后血肿扩大和钩回疝导致患者死亡。既往病史包括肝移植及长期使用环孢素、因环孢素导致的血栓性血小板减少性紫癜(TTP)特征、1型糖尿病以及因糖尿病肾病导致的急性肾衰竭。有2个月高血压病史,对治疗反应不佳。尸检发现枕叶有局灶性皮质出血,双侧白质变色,皮质下区域未受累。显微镜检查显示白质苍白伴实质囊肿、血管周围间隙增宽和局灶性急性出血,符合急性高血压继发水肿表现。皮质出血与血管内血栓及纤维蛋白渗出有关,还伴有微梗死,归因于TTP。枕叶病变反映了后部白质脑病综合征(PLS)合并TTP的皮质病变。PLS通常通过枕叶低密度影在影像学上诊断,且是可逆的,因此很少进行尸检病理检查。在某些情况下,TTP可能易引发PLS的发生。

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