首页> 外文期刊>European Journal of Pediatric Surgery Reports >Diagnosis and Management of an Isolated Pediatric Plexiform Neurofibroma Involving the Hepatic and Celiac Plexus Using Multimodality Approach: Problem Solving with Diffusion-Weighted Magnetic Resonance Imaging
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Diagnosis and Management of an Isolated Pediatric Plexiform Neurofibroma Involving the Hepatic and Celiac Plexus Using Multimodality Approach: Problem Solving with Diffusion-Weighted Magnetic Resonance Imaging

机译:使用多模态方法诊断和处理涉及肝和腹腔神经丛的小儿多形神经纤维瘤:弥散加权磁共振成像解决问题

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Plexiform neurofibroma with involvement of the gastrointestinal tract is a very rare entity in children. Here, we present a rather unique case of a 9-year-old boy with no clinical signs or features of neurofibromatosis type 1. A periportal mass lesion was incidentally found after performing an ultrasound in this previously healthy child. Computed tomographic scan was subsequently performed which showed a low-density mass in a periportal distribution with extension along the celiac axis. Because the findings were nonspecific, a pre- and postcontrast magnetic resonance imaging of the abdomen was performed which included diffusion-weighted imaging. The lesion was then confirmed to be a plexiform neurofibroma with open biopsy. Management of plexiform neurofibromas varies widely. Given the extensive nature of the lesion, managing the patient with follow-up rather than surgical excision was favored.
机译:小肠状神经纤维瘤累及胃肠道是儿童中非常罕见的实体。在这里,我们介绍了一个9岁男孩的相当独特的病例,该男孩没有1型神经纤维瘤病的临床体征或特征。在这个先前健康的孩子中进行了超声检查后,偶然发现了门静脉周围包块病变。随后进行了计算机断层扫描,显示了沿腹腔轴延伸的低密度肿块在门静脉分布中。由于发现是非特异性的,因此进行了腹部造影前后的磁共振成像,包括弥散加权成像。然后证实该病灶为开腹活检的丛状神经纤维瘤。丛状神经纤维瘤的管理差异很大。考虑到病变的广泛性,因此建议对患者进行随访而不是手术切除。

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