首页> 外文期刊>European Spine Journal >The aetiology behind torticollis and variable spine defects in patients with Müllerian duct/renal aplasia-cervicothoracic somite dysplasia syndrome: 3D CT scan analysis
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The aetiology behind torticollis and variable spine defects in patients with Müllerian duct/renal aplasia-cervicothoracic somite dysplasia syndrome: 3D CT scan analysis

机译:Müllerian导管/肾发育不全-子宫颈胸膜发育不良综合征患者的斜颈和可变性脊柱缺损的病因:3D CT扫描分析

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The aim of the article is fourfold; firstly, to detect the aetiology of torticollis in patients with Müllerian duct/renal aplasia-cervicothoracic somite dysplasia syndrome; secondly, spine pathology in Müllerian duct/renal aplasia-cervicothoracic somite dysplasia syndrome varies considerably from one patient to another and there are remarkable differences in severity and localization; thirdly, mismanagement of congenital spine pathology is a frequent cause of morbid/fatal outcome; and fourthly, the application of prophylactic surgical treatment to balance the growth of the spine at an early stage is mandatory. Reformatted CT scans helped in exploring the craniocervical and the entire spine in these patients. The reason behind torticollis ranged between aplasia of the posterior arch of the atlas, assimilation of the atlas and extensive fusion of the lower cervical vertebrae (bilateral failure of segmentation) in four patients; in one patient, in addition to the hypoplastic posterior arch of the atlas, we observed ossification of the anterior and the posterior longitudinal spinal ligaments giving rise to a block vertebrae-like suggestive of early senile ankylosing vertebral hyperostosis (Forestier disease). Scoliosis at different spine levels was attributable to variable spine defects. Pelvic ultrasound showed the classical renal agenesis in four patients; whereas in one patient, the MRI showed pelvic cake kidney (renal fused ectopia) associated with ovarian, uterine and vaginal abnormalities. This is the first exploratory study on the craniocervical and the entire spine in a group of patients with MURCS association.
机译:这篇文章的目的有四个方面。首先,检测穆勒氏管/肾发育不全-宫颈胸膜囊性不典型增生综合征患者斜颈的病因;其次,穆勒氏管/肾发育不全-宫颈胸膜发育不良综合征的脊柱病理学因人而异,严重程度和位置差异很大。第三,先天性脊柱病理的管理不善是病态/致命结局的常见原因。第四,必须尽早采用预防性外科手术治疗以平衡脊柱的生长。重新格式化的CT扫描有助于探查这些患者的颅颈和整个脊柱。在四例患者中,斜颈背后的原因包括寰椎后弓发育不全,寰椎同化和下颈椎广泛融合(双侧分割失败)。在一名患者中,除了寰椎后突发育不良外,我们还观察到前,后纵韧带骨化,形成了类似椎骨的块状,提示早老的强直性椎体肥大(Forestier病)。不同脊柱水平的脊柱侧弯可归因于各种脊柱缺陷。盆腔超声检查显示有4例患者出现经典的肾不发育。而一名患者的MRI显示骨盆蛋糕肾(肾融合性近视)与卵巢,子宫和阴道异常有关。这是对一组具有MURCS关联的患者的颅颈和整个脊柱的首次探索性研究。

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