期刊文献+

脑膜血管瘤病变伴发颅内动脉瘤形成一例并文献复习 被引量:2

Meningioangiomatosis complicated with intracranial aneurysm formation: a case report and literature review
下载PDF
导出
摘要 目的探讨1例脑膜血管瘤病变(MA)伴发颅内动脉瘤的临床特征及治疗策略。方法回顾性分析中山大学附属第一医院神经外科收治的1例形成颅内动脉瘤的MA患者的临床资料,实施急诊开颅大脑中动脉瘤夹闭、颅内血肿清除术,并将手术中动脉瘤周围脑膜脑组织做病理学检查。结果 MA伴发颅内动脉瘤患者镜检提示脑膜增厚,梭形细胞围绕脑膜和皮质内增生的血管周围形成环状、栅栏状结构。免疫组化结果示增生的血管及血管周围成纤维细胞样梭形细胞弥漫性vimentin阳性;增生的血管内皮细胞CD99、CD34阳性;病灶内残存胶质细胞示神经胶质原纤维酸性蛋白质阳性。结论 MA伴发动脉瘤形成的脑膜血管瘤病罕见,患者脑皮质血管畸形,血管条件差,动脉瘤形状极不规则,出血风险较高,可显微外科手术切除受累脑膜脑组织并夹闭动脉瘤。 Objective To investigate the clinical features and therapeutic strategies of one patient with meningioangiomatosis ( MA ) complicated with intracranial aneurysm formation. Methods The clinical data of one patient with aneurysm-formed MA admitted to the Department of Neurosurgery,the First Affiliated Hospital of Sun Yat-sen University was analyzed retrospectively. The patient received emergency craniotomy and middle cerebral artery aneurysm clipping and evacuation of intracranial hematoma. The meningeal tissue around the aneurysm was taken for pathological examination. Results Microscopy revealed meningeal thickening in the patient with MA accompanied with intracranial aneurysm. Spindle cells around the meninges and perivascular tissue of cortical hyperplasia formed an annular and fence-like structure. The results of immunohistochemistry showed the hyperplastic vessels and perivascular fibroblast like spindle cells diffuse vimentin-positive;the hyperplastic vascular endothelial cells CD99,CD34 were positive;and the residual glial cells in the lesions showed glial fibrillary acidic protein positive. Conclusion MA complicated with intracranial aneurysm is rare. The vascular condition is poor. The shape of aneurysm is irregular,and the risk of bleeding is high. Excise the involved meningeal tissue and clip the aneurysm with microsurgical operation is the resonable treatment.
出处 《中国脑血管病杂志》 CAS 2014年第8期431-435,共5页 Chinese Journal of Cerebrovascular Diseases
关键词 颅内动脉瘤 显微外科手术 脑膜血管瘤病 临床特点 Intracranial aneurysm Microsurgery Meningioangiomatosis Clinical features
  • 相关文献

参考文献14

  • 1Jennett B, Bond M. Assessment of outcome after severebrain damage[ J]. Lancet ,1975,1 (7905 ) :480-484.
  • 2Bassoe P, Nuzum F. Report of a case of central andperipheral neurofibromatosis [ J ] . J Nerv Ment Dis.
  • 3Perry A,Kurtkaya-Yapicier 0,Scheithauer BW,et al.Insights into meningioangiomatosis with and withoutmeningioma: a clinicopathologic and genetic series of24 cases with review of the literature [ J ]. Brain Pathol,2005,15(1) :55-65.
  • 4Kleihues P,Cavenee WK.神经系统肿瘤病理学和遗传学[M].李青,徐庆中,译.北京:人民卫生出版社,2006:260-263.
  • 5Deb P, Gupta A, Sharma MC’et al. Meningioangiomatosiswith meningioma : an uncommon association of a rareentity-report of a case and review of the literature [ J ].Childs Nerv Syst,2006,22(1) :78-83.
  • 6Omeis I,Hillard VH,Braun A,et al. Meningioangiomatosisassociated with neurofibromatosis ; report of 2 cases in asingle family and review of the literature [ J ]. Surg Neurol,2006,65(6) :595-603.
  • 7徐建堃,杜建新.脑膜血管瘤病的临床特点(附1例报道)[J].临床神经外科杂志,2009,6(1):17-18. 被引量:4
  • 8Arcos A,Serramito RM,Santin JM,et al. Meningioangiom-atosis :clinical-radiological features and surgical outcome[J]. Neurocirugia (Astur) ,2010,21 (6) :461-466.
  • 9Kim WY,Kim IO,Kim S,et al. Meningioangiomatosis:MRimaging and pathological correlation in two cases[ J].Pediatr Radiol,2002,32(2) :96-98.
  • 10Tacconi L,Thom M,Symon L. Cerebral meningioangioma-tosis :case report[ J]. Surg Neurol, 1997 ,48(3) :255-260.

二级参考文献69

  • 1朱海青,李南云,沈静,周晓军,周金宝.中枢神经系统神经节细胞胶质瘤/神经节细胞瘤的病理特点[J].临床神经病学杂志,2005,18(3):188-190. 被引量:11
  • 2Paringon C R, Graves V B, Megstrand L R. Meningioangiomatosis [J]. Am J Neuroracliol, 1991, 12:549-552.
  • 3Bassoe P, Nuzum F. Report of a case of central and peripheral neurofibromatosis[J]. J Nerv Ment Dis, 1915, 42:785-796.
  • 4Worster-Drought C, Dickson WEe, McMenemy W H. Multiple meningeal and perineural tumors with analogous changes in the glia and ependyma[J]. Brain, 1937, 60:85-117.
  • 5Stemmer-Rachamimov k O, Horgaa N A, Taratuto A C, et al. Meningioangiomatosis is associated with neurofibromatosis 2 but not with somatic alterations of the NF2 gene[J]. J Neuropathol Exp Neurol, 1997,56:485-489.
  • 6Wang Y, Gao X, Yao ZW, et aI. Histopathological study of five cases with sporadic meningioangiomatosis [J]. Neuropathology, 2006, 26(3): 249-256.
  • 7Perry A, Kurtkaya-Yapicier O, Scheithauer BW, et al. Insights into meningioangiomatosis with and without meningioma: a clinicopathologic and genetic series of 24 cases with review of the literature[J]. Brain Pathol, 2005, 15 (1):55-65.
  • 8Halpe J, Scheitauer BW, Okazaki H, et al. Meningioangiomatosis: a report of six cases with special reference to the occurrence of neurofibrillary tangles[J]. J Neuropathol Exp Neurol, 1986,45:426-446.
  • 9Park M S, Suh D C, Choi W S, et al. Multifocal meningioangiomatosis:a report of two cases[J].Am J Neuroradiol, 1999, 20 (4) : 677-680.
  • 10Blumenthal D, Berho M, Bloomfield S, et al. Childhood meningioma associated with meningiomatosis: case report [J].J Neurosurg ,1993,78:287-289.

共引文献13

同被引文献22

引证文献2

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部