Rare giant primary intracranial angioleiomyoma in lateral ventricle: a case report and the literature review

被引：3

作者：

Ding, Jiangwei ^{[1
,2
]}

Wang, Feng ^{[1
,2
]}

Li, Yuan ^{[3
]}

Sun, Tao ^{[1
,2
]}

机构：

[1] Ningxia Med Univ, Ningxia Key Lab Cerebrocranial Dis, Yinchuan, Ningxia, Peoples R China

[2] Ningxia Med Univ, Dept Neurosurg, Gen Hosp, Yinchuan, Ningxia, Peoples R China

[3] Zhengzhou Univ, Dept Neurosurg, Affiliated Hosp 1, Zhengzhou, Henan, Peoples R China

来源：

BRITISH JOURNAL OF NEUROSURGERY | 2020年 / 34卷 / 06期

关键词：

Intracranial vascular leiomyosarcoma; nonmalignant tumor; microsurgical; MRI; immunohistochemistry; CAVERNOUS SINUS ANGIOLEIOMYOMA; INFRATENTORIAL ANGIOLEIOMYOMA; DIAGNOSIS;

D O I：

10.1080/02688697.2020.1719037

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Background: Angioleiomyomas are benign tumors and can occur in subcutaneous tissues all over the body, and lower extremities are more common. Primary intracranial angioleiomyomas are rare. We present a case of intracranial angioleiomyoma and review the literature. Case description: A 35-year-old Chinese women presented with one-year history of the left leg claudication. MRI revealed a 6.3 x 7.4 x 5.4 cm lesion located in the lateral ventricle, which, to our knowledge is the first lateral ventricle ALM reported. The tumor was resected. The pathological results were consistent with angioleiomyoma. Hemiplegia of left limb was found during post-operative period and no recurrence was found during five month of follow-up. Conclusion: ALM is a rare intracranial tumor but can occur.

引用

页码：710 / 714

页数：5

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