Kimura T, Sako K, Ishizaki T, Hashizume K, Yonemasu Y, Hamada O
Department of Neurosurgery, Asahikawa Medical College, Japan.
No To Shinkei. 1996 Oct;48(10):955-9.
We reported two patients from the same family underwent operation for neurological symptoms due to vascular lesions that were proved on pathological examination to be cavernous angiomas. Case 1, a 64-year-old woman was admitted to our hospital because of paraparesis. MRI revealed a mass lesion with high signal intensity in T1 and T2 weighted images at T3-4 level. Complete excision was carried out and diagnosis of cavernous angioma was made. Three years later, she experienced a mild headache and dizziness. CT scan demonstrated a subcortical hematoma in the right frontal lobe. Postoperative pathological diagnosis was cavernous angioma. Case 2, a 65-year-old woman (younger sister of case 1) was operated for the tumor of spinal cord, and diagnosed as a cavernous angioma. Two years later, she developed diplopia and ataxic gait. MRI showed multiple cavernous angioma in the brain including pons. Pontine lesion which was responsible for this episode was removed, and diagnosis was a cavernous angioma histopathologically.
我们报告了来自同一家庭的两名患者,他们因血管病变出现神经症状而接受手术,病理检查证实为海绵状血管瘤。病例1,一名64岁女性因双下肢轻瘫入住我院。MRI显示T3 - 4水平T1加权和T2加权图像上有一个高信号强度的肿块病变。进行了完整切除,诊断为海绵状血管瘤。三年后,她出现轻度头痛和头晕。CT扫描显示右额叶皮质下血肿。术后病理诊断为海绵状血管瘤。病例2,一名65岁女性(病例1的妹妹)因脊髓肿瘤接受手术,诊断为海绵状血管瘤。两年后,她出现复视和共济失调步态。MRI显示脑部包括脑桥有多个海绵状血管瘤。切除了导致此次发作的脑桥病变,组织病理学诊断为海绵状血管瘤。