A ventral brainstem neurenteric cyst – A case report and review of the pre-brainstem location

Q3 Medicine
Samuel Sequeira Lemos, Maria Inês Sá, C. Casimiro, Carla Guerreiro, Claudia Faria
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Abstract

Neurenteric cysts are uncommon, benign endoderm-derived lesions that result from aberrant embryologic development of the notochord. They are typically located in the intradural extramedullary spinal cord and rarely located intracranially. Contrary to spinal-located cysts, intracranial cysts are rarer in the pediatric population. Clinically, they may present with symptoms of mass effect, or they can be incidentally discovered. A 10-year-old healthy female child presented with recurrent headaches. The physical and neurological examination was unremarkable. Brain magnetic resonance imaging (MRI) showed a well-demarcated lesion anterior to the pontomedullary junction with striking T1 and T2/T2 fluid-attenuated inversion recovery high-signal intensity and a small rounded nodule within of low signal on T1, T2, and T2*. On initial conservative strategy with serial brain MRI, there was a progressive enlargement of the lesion with significant mass effect on the brainstem. The patient underwent a right retrosigmoid craniotomy, and the cyst wall was fenestrated and drained. Part of the cyst wall and the solid nodule were adherent to the brainstem and basilar artery and were not removed. The histologic findings were consistent with the diagnosis of a benign endodermal cyst. The postoperative period was uneventful. We report a successful surgical treatment of this rare congenital cyst located in the ventral brainstem. We present pre-and post-operative imaging findings, intraoperative microscopic images of the procedure, and a brief review of relevant clinical literature on the topic.
腹侧脑干神经节囊肿--病例报告和脑干前位置回顾
神经节囊肿是一种不常见的内胚层良性病变,由脊索的胚胎发育异常引起。它们通常位于硬膜外脊髓内,很少位于颅内。与位于脊髓的囊肿相反,颅内囊肿在儿童中较为罕见。临床上,囊肿可能伴有肿块症状,也可能是偶然发现的。体格检查和神经系统检查均无异常。脑磁共振成像(MRI)显示,在桥髓交界处前方有一个分界清楚的病灶,T1和T2/T2液相衰减反转恢复高信号强度,内部有一个圆形小结节,T1、T2和T2*均为低信号。在最初的保守治疗策略和连续的脑部 MRI 检查中,病灶逐渐扩大,并对脑干产生了明显的肿块效应。患者接受了右侧后枕部开颅手术,囊肿壁被切开并引流。部分囊壁和实性结节与脑干和基底动脉粘连,未被切除。组织学检查结果与良性内皮囊肿的诊断一致。我们报告了对这种位于脑干腹侧的罕见先天性囊肿的成功手术治疗。我们报告了这例位于腹侧脑干的罕见先天性囊肿的成功手术治疗,介绍了手术前后的影像学检查结果、术中显微图像以及相关临床文献的简要回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
623
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