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首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >A peri-trigonal giant tumefactive cavernous malformation: case report and review of literature.
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A peri-trigonal giant tumefactive cavernous malformation: case report and review of literature.

机译:三角周围巨肿性海绵状畸形:病例报告及文献复习。

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摘要

INTRODUCTION: Giant cavernous malformations (GCMs) constitute an uncommon entity in the diagnostic armamentarium of the neurosurgeon. We report a 3-year-old boy with a GCM in the peri-trigonal region and review 13 other paediatric cases previously reported in literature. CASE: A 3-year-old boy presented with right-sided hemiparesis and features of raised intracranial pressure of short duration. Computed tomography showed a large left peri-trigonal mass with a bleed. Magnetic resonance imaging showed associated perilesional edema and mass effect, rendering the lesion a tumefactive appearance. He underwent total excision of the lesion, with subsequent recovery of hemiparesis. Histopathology was reported as a cavernoma. DISCUSSION: The clinico-radiological presentation of GCM is discussed based on a case report and relevant cases in literature. Good surgical outcome can be expected with total microsurgical excision. CONCLUSION: A giant cavernous malformation should be one of the differentials of a lesion with a tumefactive clinico-radiological presentation in children. There should be a high index of suspicion for such a diagnosis, especially when the lesion does not enhance with contrast. This is the third case report in paediatric literature describing a periventricular location of this unusual lesion.
机译:简介:巨大的海绵状畸形(GCM)在神经外科医生的诊断武器库中构成罕见的实体。我们报告了一个3岁男孩在三角区域周围有GCM,并回顾了以前文献中报道的其他13例儿科病例。病例:一个3岁男孩,表现为右侧偏瘫和短期内颅内压升高的特征。计算机断层扫描显示左大三角周围肿块伴有出血。磁共振成像显示相关的病灶周围水肿和肿块效应,使病灶呈肿块状。他对病变进行了完全切除,随后恢复了偏瘫。据报道组织病理学为海绵状瘤。讨论:基于病例报告和文献中的相关病例,讨论了GCM的临床放射学表现。完全显微手术切除有望获得良好的手术效果。结论:巨大的海绵状畸形应该是儿童具有肿瘤性临床放射学表现的病变的区别之一。对于这种诊断,应该有很高的怀疑指数,尤其是当病变没有形成对比增强时。这是儿科文献中的第三例病例报告,描述了这种异常病变的脑室周围位置。

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