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在罕见情况下,丝状囊肿可能会增大,尤其是与丝状脂肪瘤相关时。

Filar cysts in rare cases may progress in size, particularly when associated with filar lipoma.

作者信息

Seo Kyoichi, Oguma Hirofumi, Furukawa Rieko, Gomi Akira

机构信息

Department of Neurosurgery, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi, Japan.

Department of Pediatric Medical Imaging, Jichi Children's Medical Center Tochigi, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi, Japan.

出版信息

Childs Nerv Syst. 2019 Jul;35(7):1207-1211. doi: 10.1007/s00381-019-04148-6. Epub 2019 Apr 10.

DOI:10.1007/s00381-019-04148-6
PMID:30972496
Abstract

PURPOSE

Filar 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.

METHODS

We retrospectively analyzed 396 patients with lumbosacral skin stigmata. Patients who were younger than 1 month old at reference underwent US initially, and those older than 1 month of age underwent magnetic resonance imaging (MRI) at the age of 5-12 months. Patients with an FC in the US underwent subsequent MRI at the age of 5-12 months. Patients with an FC were followed clinically for at least 3 years.

RESULTS

FCs 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 5-12 months, 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.

CONCLUSIONS

Our 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.

摘要

目的

丝状囊肿(FCs)在新生儿脊柱超声检查(US)中偶然被发现。由于FCs通常无症状,其临床意义在文献中尚未得到广泛讨论。本研究旨在调查FCs的临床特征,并鉴别需要关注的FCs。

方法

我们回顾性分析了396例腰骶部皮肤有体征的患者。最初对年龄小于1个月的患者进行超声检查,年龄大于1个月的患者在5至12个月时接受磁共振成像(MRI)检查。超声检查发现有FCs的患者在5至12个月时接受后续MRI检查。对有FCs的患者进行至少3年的临床随访。

结果

56例(14.1%)患者发现有FCs。在最初接受超声检查的195名儿童中,49例(25.1%)发现有FCs。最初接受MRI检查的7名儿童中发现有FCs。在5至12个月时接受MRI检查的50例有FCs的儿童中,20例(40%)的FCs自然消退,30例(60%)的FCs持续存在。这30例患者中有2例FCs大小有进展,且在这两种情况下,FCs均与丝状脂肪瘤相关;然而,切除的囊肿并非肿瘤性,且没有明显的临床意义。

结论

我们的研究描述了丝状囊肿的临床特征。三分之二的FCs在婴儿晚期持续存在。随访FCs的最佳MRI序列是重度T2加权图像。

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引用本文的文献

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Utility of routine mid-trimester fetal ultrasound scan in detecting filar cysts and follow-up outcomes.常规中期妊娠胎儿超声扫描在检测丝虫囊肿及随访结果中的应用。
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Secondary Neurulation Defects: Retained Medullary Cord.

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