Cystic meningioangiomatosis in a middle-aged male patient: Case report and literature review

被引：0

作者：

Chen, Long ^{[1
]}

Sun, Pengju ^{[1
]}

Starkweather, Clara ^{[2
]}

Koffie, Robert M. ^{[2
]}

Fan, Miaojing ^{[3
]}

Zhu, Siyang ^{[1
]}

Gao, Zhibo ^{[1
]}

机构：

[1] Anhui Med Univ, Fuyang Clin Coll, Fuyang Peoples Hosp, Dept Neurosurg, 501 Sanqing Rd, Fuyang 236006, Anhui, Peoples R China

[2] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurosurg, 55 Fruits St, Boston, MA 02115 USA

[3] Anhui Med Univ, Fuyang Clin Coll, Fuyang Peoples Hosp, Dept Pathol, Fuyang 236006, Anhui, Peoples R China

来源：

INTERDISCIPLINARY NEUROSURGERY-ADVANCED TECHNIQUES AND CASE MANAGEMENT | 2020年 / 21卷

关键词：

Meningioangiomatosis; Meningioma; Epilepsy; Cystic lesion; MENINGIOMA;

D O I：

10.1016/j.inat.2020.100714

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Meningioangiomatosis (MA) is a clinically rare intracranial lesion that occurs sporadically or develops as a component of neurofibromatosis-2 (NF-2). MA can present as either solid or cystic lesions. Cystic MA is extremely rare, with no specific manifestations on imaging, but can present clinically as a seizure inciting focus. We report a rare case of cystic MA that presented as intractable epilepsy. The patient was a 47-year-old male construction worker with no history of genetically predisposing disorders. Magnetic resonance imaging (MRI) showed a circular and well-defined, low-density lesion in the right temporal lobe, with an enhancing mural nodule. Surgical resection was performed, and histologic pathology confirmed MA. We review the literature on identification, diagnosis, and management strategies for MA.

引用

页数：5

共 19 条

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