Suppr超能文献

[脑内海绵状血管瘤的家族性发病情况]

[Familial occurrence of intracerebral cavernous angioma].

作者信息

Kim S H, Mitsuno K, Ishikawa M, Kikuchi H, Motosaki T, Yamamoto T

机构信息

Department of Neurosurgery, Ako Municipal Hospital, Hyogo, Japan.

出版信息

No Shinkei Geka. 1989 Jan;17(1):75-9.

PMID:2651957
Abstract

This article reported a familial occurrence of intracerebral cavernous angioma in four members of one generation diagnosed by X-ray CT, MRI or operative specimen. Case 1, a 34-year-old female, was examined just after an episode of sudden convulsive seizure. On examination, she had a cutaneous angioma without any neurological deficit. X-ray CT revealed a high density mass lesion in the left frontal lobe, and MRI demonstrated a mass lesion in the chronic stage with an old hematoma circumscribed by hypointensity ring indicating peripheral hemosiderosis. Complete excision was carried out and a diagnosis of cavernous angioma was made after histological examination. Case 2, the 37-year-old brother of Case 1, suddenly developed left hemiparesis and hypesthesia with severe headache. X-ray CT revealed a high density mass in the right parietal lobe and two other calcifications. The right parietal lesion was excised and a histopathological diagnosis of cavernous angioma with intracerebral hematoma was made. Case 3, the 49-year-old sister of Case 1, suddenly fell into a coma and was admitted immediately. X-ray CT revealed a large pontine hemorrhage. She died on the 4th day of hospitalization without operative treatment. Necropsy was not carried out. Case 4, the 39-year-old sister of Case 1, was asymptomatic, however, she was examined on the supposition of a familial occurrence of intracerebral cavernous angioma. On examination, it was found she had multiple cavernous angioma without any neurological deficit. X-ray CT revealed parietal intracerebral calcification. MRI demonstrated a mass lesion with peripheral hypointensity ring in the right parietal lobe, and another small lesion in the pons.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文报道了同一代的四名家庭成员发生家族性脑内海绵状血管瘤,通过X线计算机断层扫描(X-ray CT)、磁共振成像(MRI)或手术标本确诊。病例1,一名34岁女性,在突发惊厥发作后接受检查。检查发现她有皮肤血管瘤,无任何神经功能缺损。X线CT显示左额叶有高密度肿块病变,MRI显示为慢性期肿块病变,有陈旧性血肿,周围有低信号环,提示外周含铁血黄素沉着。进行了完整切除,组织学检查后诊断为海绵状血管瘤。病例2,病例1的37岁哥哥,突然出现左侧偏瘫、感觉减退并伴有严重头痛。X线CT显示右顶叶有高密度肿块及另外两处钙化。切除了右顶叶病变,组织病理学诊断为海绵状血管瘤伴脑内血肿。病例3,病例1的49岁姐姐,突然昏迷并立即入院。X线CT显示桥脑大量出血。她在住院第4天未接受手术治疗死亡。未进行尸检。病例4,病例1的39岁姐姐,无症状,但基于家族性脑内海绵状血管瘤的推测接受了检查。检查发现她有多发海绵状血管瘤,无任何神经功能缺损。X线CT显示顶叶脑内钙化。MRI显示右顶叶有一肿块病变,周围有低信号环,桥脑还有另一小病变。(摘要截选于250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验