Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway; Department of Radiology and Nuclear Medicine, Oslo University Hospital, Ullevål, PO BOX 4956 Nydalen, Oslo 0424, Norway.
Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway; Department of Cardiothoracic Surgery, Oslo University Hospital, Oslo, Norway.
Spine J. 2019 Aug;19(8):1412-1421. doi: 10.1016/j.spinee.2019.04.010. Epub 2019 Apr 15.
Dural ectasia is widening of the dural sac often seen in patients with Marfan syndrome and other hereditary connective tissue disorders. Dural ectasia can cause specific symptoms and is associated with surgical complications. The knowledge on how and at which age dural ectasia develops is incomplete. There is no established gold standard for diagnosing dural ectasia, making it difficult to compare results from different studies.
Our primary aim was to explore whether the radiological findings of dural ectasia changed after 10 years in an adult cohort with suspected Marfan syndrome. Our secondary aim was to re-evaluate the radiological criteria of dural ectasia.
Prospective cohort study.
Sixty-two persons from a cross-sectional study of 105 persons with suspected Marfan syndrome were included in a 10-year follow-up of dural ectasia. Forty-six were diagnosed with Marfan syndrome, 7 with Loeys-Dietz syndrome, and 5 with other hereditary connective tissue disorders. For comparison 64 matched hospital controls were evaluated.
Previously used radiological criteria for dural ectasia based on quantitative measurements of the lumbosacral spine.
MRI of the lumbosacral spine was performed if not contraindicated, and if so then CT was performed. Differences in the study group between baseline and follow-up were assessed with paired Student t test, Wilcoxon rank signed test, and McNemar test. Receiver operating characteristic curves were constructed to assess the ability of radiological measurement to differentiate between the study and control group.
Fifty-two of 58 patients with hereditary connective tissue disorders and 11 controls had dural ectasia at follow-up. Forty-five Marfan patients had dural ectasia at follow-up vs. 41 at baseline. Five Loeys-Dietz patients had dural ectasia at follow-up vs. four at baseline. Twenty-four Marfan and 2 Loeys-Dietz patients had anterior sacral meningocele at follow-up, compared with 21 and 1, respectively, at baseline. Three Marfan patients developed herniation of a nerve root sleeve during follow-up. This was not seen in other individuals. The dural sac ended significantly lower at follow-up, and the dural sac ratio at level L5 was significantly increased from baseline in the Marfan patients.
In Marfan and Loeys-Dietz syndrome, dural ectasia may present or worsen during adulthood. The cut-off value of dural sac ratio at level S1 is suggested elevated to 0.64. The results from the present study may help as guidance for appropriate follow-up of patients with dural ectasia.
硬脑膜扩张症是硬脑膜囊的扩张,常见于马凡综合征和其他遗传性结缔组织疾病患者。硬脑膜扩张可引起特定症状,并与手术并发症相关。关于硬脑膜扩张如何以及在什么年龄发展的知识尚不完全。目前尚无诊断硬脑膜扩张的金标准,这使得不同研究的结果难以比较。
我们的主要目的是探讨疑似马凡综合征的成年患者队列中,硬脑膜扩张的放射学表现是否在 10 年后发生变化。我们的次要目的是重新评估硬脑膜扩张的放射学标准。
前瞻性队列研究。
从 105 例疑似马凡综合征患者的横断面研究中,62 例患者纳入硬脑膜扩张 10 年随访。46 例被诊断为马凡综合征,7 例为 Loeys-Dietz 综合征,5 例为其他遗传性结缔组织疾病。为了比较,还评估了 64 例匹配的医院对照。
先前基于腰骶脊柱定量测量的硬脑膜扩张放射学标准。
如果没有禁忌症,进行腰骶部 MRI,如果有,则进行 CT。使用配对学生 t 检验、Wilcoxon 秩和检验和 McNemar 检验评估研究组在基线和随访之间的差异。构建受试者工作特征曲线以评估放射学测量区分研究组和对照组的能力。
58 例遗传性结缔组织疾病患者和 11 例对照组中有 52 例在随访时存在硬脑膜扩张。45 例马凡综合征患者在随访时存在硬脑膜扩张,而基线时为 41 例。5 例 Loeys-Dietz 患者在随访时存在硬脑膜扩张,而基线时为 4 例。24 例马凡综合征和 2 例 Loeys-Dietz 患者在随访时出现前骶膜神经囊膨出,而基线时分别为 21 例和 1 例。3 例马凡综合征患者在随访期间出现神经根袖套疝,而其他患者未出现。马凡综合征患者的硬脑膜囊在随访时明显下降,L5 水平的硬脑膜囊比在基线时明显增加。
在马凡综合征和 Loeys-Dietz 综合征中,硬脑膜扩张可能在成年期出现或加重。建议将 S1 水平硬脑膜囊比的截断值升高至 0.64。本研究的结果可能有助于指导硬脑膜扩张患者的适当随访。