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两例颅内纤维肌性发育不良患者,反复血管造影显示病变进展

[Two cases of intracranial fibromuscular dysplasia whose repeated angiography disclosed progression of the lesion].

作者信息

Fujimoto S, Kayama T, Ogawa A, Sakurai Y, Yoshimoto T, Suzuki J

机构信息

Neurosurgical Department, Stroke Center of Sendai National Hospital.

出版信息

No To Shinkei. 1987 Oct;39(10):937-45.

PMID:3325087
Abstract

Fibromuscular dysplasia (FMD) is well known owing to the characteristic angiographical finding of a "string of beads" appearance, but intracranial involvement with this disease is extremely rare. Moreover, to our knowledge, only seven cases that had repeated angiograms disclosed progression of FMD lesion in the literature. Such cases of intracranial FMD which showed progression in the follow-up angiography are reported. Case 1: A 8-year-old boy was referred to our hospital because of aphasia and right hemiplegia following right hemiconvulsion. Left carotid angiography on the 7th day from the onset revealed a "string of beads" appearance involving the left middle cerebral artery from M1 to M2 portion. He was treated with low molecular dextran, urokinase and steroid. After these drugs were administered, his speech was normalized. A repeat left angiogram performed two months later disclosed definite increase in the degree of stenosis associated with FMD. Perivascular sympathectomy around common and internal carotid artery and superior cervical ganglionectomy on the left side carried out on the 70th day from the onset. Postoperative left carotid angiogram showed improvement of the stenosis markedly, and the motor disturbance was improved gradually. Case 2: A 34-year-old woman presented with head dullness and disorientation suddenly. Left carotid angiogram on the third day from the onset showed a "string of beads" appearance from C1 to M1 portion. Follow-up angiography three days later revealed some progression of the stenosis. Furthermore a repeat left angiogram disclosed occlusion of left internal carotid artery at the C2 portion. Left STA-MCA bypass surgery was performed on the 61st day from the onset.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

纤维肌发育不良(FMD)因其典型的血管造影表现“串珠样”而广为人知,但该病累及颅内极为罕见。此外,据我们所知,文献中仅有7例重复血管造影显示FMD病变进展的病例。本文报告了此类在随访血管造影中显示进展的颅内FMD病例。病例1:一名8岁男孩因右侧半身惊厥后失语和右侧偏瘫被转诊至我院。发病第7天的左侧颈动脉血管造影显示“串珠样”改变,累及左侧大脑中动脉M1至M2段。给予低分子右旋糖酐、尿激酶和类固醇治疗。用药后,他的言语恢复正常。发病后两个月进行的重复左侧血管造影显示,与FMD相关的狭窄程度明显增加。发病第70天,在颈总动脉和颈内动脉周围进行血管周围交感神经切除术,并切除左侧颈上神经节。术后左侧颈动脉血管造影显示狭窄明显改善,运动障碍逐渐好转。病例2:一名34岁女性突然出现头部闷痛和定向障碍。发病第3天的左侧颈动脉血管造影显示从C1至M1段呈“串珠样”改变。三天后的随访血管造影显示狭窄有所进展。此外,重复左侧血管造影显示左侧颈内动脉C2段闭塞。发病第61天进行了左侧颞浅动脉-大脑中动脉搭桥手术。(摘要截选至250字)

相似文献

1
[Two cases of intracranial fibromuscular dysplasia whose repeated angiography disclosed progression of the lesion].两例颅内纤维肌性发育不良患者,反复血管造影显示病变进展
No To Shinkei. 1987 Oct;39(10):937-45.
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[A case report of fibromuscular dysplasia presenting symptoms like moyamoya disease: "string of beads" appearance of the pericallosal artery].[1例表现为烟雾病样症状的纤维肌发育不良病例报告:胼周动脉的“串珠样”表现]
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No Shinkei Geka. 1997 Aug;25(8):727-32.
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[Fibromuscular dysplasia with cerebral infarction in children. Case report].[儿童纤维肌发育不良伴脑梗死。病例报告]
Neurol Med Chir (Tokyo). 1989 Oct;29(10):912-6. doi: 10.2176/nmc.29.912.
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[A case of adult moyamoya disease showing fulminant clinical course associated with progression from unilateral to bilateral involvement].[一例成人烟雾病呈现暴发性临床病程并伴有从单侧受累进展至双侧受累]
No Shinkei Geka. 1997 Jan;25(1):79-84.
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[Percutaneous transluminal angioplasty in fibromuscular dysplasia of the internal carotid artery: case report].[经皮腔内血管成形术治疗颈内动脉纤维肌发育不良:病例报告]
No Shinkei Geka. 2002 Mar;30(3):301-6.
7
Intracranial fibromuscular dysplasia and stroke in children.
Neuroradiology. 1979 Aug 15;18(2):99-102. doi: 10.1007/BF00344830.
8
[Cerebral artery occlusion due to blunt cervical trauma].钝性颈部创伤所致脑动脉闭塞
No Shinkei Geka. 1989 Jun;17(6):579-84.
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Cephalic fibromuscular dysplasia in 32 patients: clinical findings and radiologic features.32例头颈部纤维肌发育异常:临床发现与影像学特征
Arch Neurol. 1981 Oct;38(10):619-22. doi: 10.1001/archneur.1981.00510100047006.
10
Intracranial fibromuscular dysplasia. Report of two cases and review of literature.颅内纤维肌性发育不良。两例报告并文献复习。
J Neurosurg Sci. 1987 Jan-Mar;31(1):13-8.