首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Filar cysts in rare cases may progress in size, particularly when associated with filar lipoma
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Filar cysts in rare cases may progress in size, particularly when associated with filar lipoma

机译:稀有病例中的裂缝囊肿可能大小,特别是当与裂纹脂肪瘤相关时

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PurposeFilar cysts (FCs) are detected incidentally on ultrasonography (US) of the neonatal spine. Their clinical significance has not been widely discussed in the literature because FCs are usually asymptomatic. This study aimed to investigate the clinical features of FCs and distinguish FCs that warrant attention.MethodsWe retrospectively analyzed 396 patients with lumbosacral skin stigmata. Patients who were younger than 1month old at reference underwent US initially, and those older than 1month of age underwent magnetic resonance imaging (MRI) at the age of 5-12months. Patients with an FC in the US underwent subsequent MRI at the age of 5-12months. Patients with an FC were followed clinically for at least 3years.ResultsFCs were identified in 56 (14.1%) patients. Of the 195 children who underwent US initially, FCs were detected in 49 (25.1%) children. FCs were detected in seven children who underwent MRI initially. Of the 50 children with FCs who underwent MRI at the age of 5-12months, FCs in 20 patients (40%) showed natural regression and FCs in 30 patients (60%) remained. Two of these 30 patients showed progression in size of the FC, and in both cases, the FCs were associated with a filar lipoma; however, the resected cysts were not neoplastic and did not have obvious clinical significance.ConclusionsOur study characterizes clinical features of filar cysts. Two-thirds of FCs remained in late infancy. The best sequence of MRI to follow-up FCs is heavily T2-weighted images.
机译:目的的囊肿(FCS)偶然地检测到新生儿脊柱的超声检查(US)。他们的临床意义尚未在文献中普遍讨论,因为FCS通常是无症状的。本研究旨在调查FCS的临床特征,并区分FCS认证的关注。方法回顾性地分析了396例Lumbosacral Skigmata患者。患者比1个旧的患者最初接受我们,并且在5-12个月的年龄接受磁共振成像(MRI)的1个年龄较大的人。美国FC的患者在5-12个月的5-12名上接受过后续MRI。临床上患有FC的患者至少3年患者。患者在56名(14.1%)患者中鉴定出来。在195名接受我们最初的儿童中,在49名(25.1%)儿童中检测到FCS。在最初接受MRI的七个孩子中检测到FCS。在50名患有5-12名MINS的FCS的50名儿童中,20名患者的FCS(40%)显示出自然的回归和30名患者的FCS(60%)。这30例患者中的两种患者的大小表现为FC的大小,并且在这两种情况下,FCS与裂纹脂肪瘤有关;然而,切除的囊肿不是肿瘤族,并且没有明显的临床意义。结论性研究表征Filar囊肿的临床特征。三分之二的FCS仍然在婴儿期末。最佳MRI序列到后续FCS是重大T2加权图像。

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