Department of Pathology, Niigata Neurosurgical Hospital, Niigata, Japan.
Department of Laboratory Medicine, Niigata Neurosurgical Hospital, Niigata, Japan.
Neuropathology. 2024 Dec;44(6):445-451. doi: 10.1111/neup.12998. Epub 2024 Aug 6.
A 55-year-old Japanese woman with a history of hypertension and right putaminal hemorrhage developed simultaneous hemorrhages in the left thalamus and putamen and died 24 h later. There were no vascular anomalies in the brain. Synaptophysin immunostaining combined with eosin azure 50 (EA50) staining clearly identified the hematoma and the surrounding brain structures. In the right cerebral hemisphere, a cystic lesion as a sequela of the usual type of hypertensive putaminal hematoma was evident. In the left cerebral hemisphere, two fresh hematomas were evident. One was a thalamic hematoma, which had destroyed the dorsal and medial structures of the thalamus, and the other was an unusual putaminal hematoma, which had destroyed the entire putamen and crossed the internal capsule and caudate nucleus. α-Smooth muscle actin immunostaining combined with EA50 and Victoria bleu staining demonstrated three ruptured arteries associated with fibrin aggregates in the anterior thalamic nucleus and anterior putamen. Some circular structures composed of fibrin, suggesting the presence of ruptured arteries in the neighborhood, were evident in the thalamus and putamen. In the putamen, ruptured arteries and circular structures were present in the lateral to medial areas. Fibrin aggregates in the anterior thalamic nucleus were more numerous than those in the putamen. On the basis of these findings, we concluded that: (i) the artery with numerous fibrin aggregates in the anterior thalamic nucleus had ruptured first, followed by the arteries distributed in other parts of the thalamus and putamen; (ii) the unusual putaminal hematoma was attributable to rupture of the arteries around the center of the putamen, which are not responsible for the usual type of hypertensive putaminal hematoma; and (iii) it is suggested that even if hypertensive hemorrhage occurs simultaneously in the ipsilateral putamen and thalamus, the usual type of hypertensive mixed-type hematoma does not form.
一位 55 岁的日本女性,有高血压和右侧壳核出血病史,同时出现左侧丘脑和壳核出血,并于 24 小时后死亡。脑部无血管畸形。突触素免疫染色结合曙红 Azure 50(EA50)染色清楚地识别了血肿和周围的脑结构。在右侧大脑半球,可见到通常类型的高血压壳核血肿的后遗症囊性病变。在左侧大脑半球,可见到两个新鲜血肿。一个是丘脑血肿,破坏了丘脑的背侧和内侧结构,另一个是不寻常的壳核血肿,破坏了整个壳核并穿过内囊和尾状核。α-平滑肌肌动蛋白免疫染色结合 EA50 和维多利亚蓝染色显示,前丘脑核和前壳核有三条破裂的动脉,伴有纤维蛋白聚集物。在丘脑和壳核中,可见一些由纤维蛋白组成的圆形结构,提示附近存在破裂的动脉。在壳核中,破裂的动脉和圆形结构位于外侧到内侧区域。在前丘脑核中,纤维蛋白聚集物比壳核中更多。基于这些发现,我们得出结论:(i)前丘脑核中含有大量纤维蛋白聚集物的动脉首先破裂,随后是分布在丘脑和壳核其他部位的动脉;(ii)不寻常的壳核血肿归因于壳核中心周围动脉的破裂,这些动脉与通常类型的高血压壳核血肿无关;(iii)建议即使同侧壳核和丘脑同时发生高血压性出血,也不会形成通常类型的高血压混合血肿。