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海绵状血管瘤在初次诊断13年后以癫痫为表现。

Cavernous angioma presenting as epilepsy 13 years after initial diagnosis.

作者信息

Murakami Kensuke, Umezawa Kunihiko, Kaimori Mitsuomi, Nishijima Michiharu

机构信息

Department of Neurosurgery, Aomori Prefectural Central Hospital, 2-2-1 Higahshi-tsukurimichi, Aomori, Japan.

出版信息

J Clin Neurosci. 2004 May;11(4):430-2. doi: 10.1016/j.jocn.2003.05.010.

DOI:10.1016/j.jocn.2003.05.010
PMID:15080966
Abstract

A 22-year-old man presented with tonic-clonic seizure and was admitted to our hospital. He had suffered from frequent headaches, and had been diagnosed with a brain tumour on MRI 13 years ago. However, neither further examination nor follow-up neuroimaging study have been performed. Computed tomography and magnetic resonance imaging demonstrated an intraaxial tumor with granular calcification in the right frontal lobe, attached to the adjacent dura mater, which was enlarged compared with the lesion on CT 13 years before. The lesion was surgically excised through right frontal craniotomy. Histopathological analysis indicated cavernous angioma. In cavernous angioma in younger children, more aggressive surgical indications than in adults may be favorable both to prevent haemorrhagic complications and to confirm pathologic diagnosis.

摘要

一名22岁男性因强直阵挛性发作入院。他曾频繁头痛,13年前MRI检查诊断为脑肿瘤。然而,此后既未进行进一步检查,也未进行后续神经影像学研究。计算机断层扫描和磁共振成像显示右额叶有一轴内肿瘤,伴有颗粒状钙化,与硬脑膜相邻,与13年前CT显示的病变相比有所增大。通过右额开颅手术将病变切除。组织病理学分析显示为海绵状血管瘤。对于年幼儿童的海绵状血管瘤,比成人更积极的手术指征可能有利于预防出血并发症和确诊病理诊断。

相似文献

1
Cavernous angioma presenting as epilepsy 13 years after initial diagnosis.海绵状血管瘤在初次诊断13年后以癫痫为表现。
J Clin Neurosci. 2004 May;11(4):430-2. doi: 10.1016/j.jocn.2003.05.010.
2
[Familial occurrence of intracerebral cavernous angioma].[脑内海绵状血管瘤的家族性发病情况]
No Shinkei Geka. 1989 Jan;17(1):75-9.
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[Multiple subpial transection after lesionectomy in an intractable epilepsy case].[难治性癫痫病例病灶切除术后的多处软膜下横切术]
No To Shinkei. 1993 Mar;45(3):277-80.
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[Intracerebral cavernous angioma].[脑内海绵状血管瘤]
Rev Neurol (Paris). 1989;145(6-7):429-36.
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Fatal giant pediatric intracranial cavernous angioma.致命性巨大儿童颅内海绵状血管瘤
Turk J Pediatr. 2006 Jan-Mar;48(1):89-92.
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[Coexistence of intracranial and spinal cavernous angiomas: case report].[颅内与脊髓海绵状血管瘤并存:病例报告]
No Shinkei Geka. 1992 Dec;20(12):1277-81.
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[A case of familial cerebral cavernous angioma and review of Japanese cases].[一例家族性脑海绵状血管瘤及日本病例回顾]
No Shinkei Geka. 2001 Apr;29(4):359-65.
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[Report on successful surgery of cavernous angioma in the dorsal part of the pons--usefulness of MRI in diagnosis].[桥脑背侧海绵状血管瘤成功手术报告——MRI在诊断中的应用价值]
No Shinkei Geka. 1987 Feb;15(2):159-64.
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A diagnostic pitfall: Angiosarcoma of the brain mimicking cavernous angioma.一个诊断陷阱:酷似海绵状血管瘤的脑血管肉瘤。
J Clin Neurosci. 2005 Aug;12(6):688-91. doi: 10.1016/j.jocn.2004.08.028.
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[Cerebral cavernous angiomas in pregnancy. Two cases and a review of literature].[妊娠期脑海绵状血管瘤。两例病例及文献综述]
Neurologia. 1995 Jun-Jul;10(6):242-5.

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