Craniotomy for a Large and Aggressive De Novo Cavernous Malformation Resection in the Basal Ganglia Region
Craniotomy for a Large and Aggressive De Novo Cavernous Malformation Resection in the Basal Ganglia Region
复制标题
开颅手术对基底神经节区域进行大面积、激进的海绵状血管瘤新生切除术
DOI:
10.1016/j.wneu.2018.06.067
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发表时间:
2018
影响因子:
2
通讯作者:
Wang Chao
中科院分区:
文献类型:
--
作者:
Yan Zhiyong;Che Shusheng;Jiao Yingbin;Wang JianPeng;Li Xingze;Wang Chao
BackgroundCerebral cavernous malformations (CCMs) are present in up to 0.5% of the general population. Although CCMs have been considered congenital lesions, numerous reports have observed de novo formations in patients with the familial form of CCM and in patients after cranial radiotherapy. Outside of these circumstances, there is scant evidence as to the potential etiologies of CCM.Case DescriptionWe present a 48-year-old woman with a medical history of endometrial hyperplasia concomitant endometrial polyps demonstrating a large de novo CCM, which grew to a large size in a period of 20 months. A previous magnetic resonance imaging scan showed no abnormalities. This CCM exhibited aggressive biological behavior characterized by recurrent overt bleeding and seizure. Histopathologic analysis confirmed the diagnosis of CCM. Here, we discuss the growth mechanisms of these lesions.ConclusionsGiven the patient's medical history and imaging findings, we propose that de novo CCMs can arise directly from angiogenic proliferation, secondary to BCL-2 overexpression from underlying causes. We hypothesize that inappropriate secretion of estrogen could have set off a genetic cascade with attendant endothelial proliferation.Thus, female hormones may play an important role in influencing the biological behavior of CCMs. The relationship between estrogen and CCM needs further investigation.