Menezes Arnold H, Fenoy Kathleen A
Department of Neurosurgery, University of Iowa Carver College of Medicine, Iowa City, Iowa 52242, USA.
Neurosurgery. 2009 May;64(5):945-53; discussion 954. doi: 10.1227/01.NEU.0000345737.56767.B8.
Developmental remnants around the foramen magnum, or proatlas segmentation abnormalities, have been recorded in postmortem studies but very rarely in a clinical setting. Because of their rarity, the pathological anatomy has been misunderstood, and treatment has been fraught with failures. The objectives of this prospective study were to understand the correlative anatomy, pathology, and embryology and to recognize the clinical presentation and gain insights on the treatment and management.
Our craniovertebral junction (CVJ) database started in 1977 and comprises 5200 cases. This prospective study has retrieval capabilities. Neurodiagnostic studies changed with the evolution of imaging. Seventy-two patients were recognized as having symptomatic proatlas segmentation abnormalities.
Ventral bony masses from the clivus or medial occipital condyle occurred in 66% (44/72), lateral or anterolateral compressive masses in 37% (27 of 72 patients), and dorsal bony compression in 17% (12 of 72 patients). Hindbrain herniation was associated in 33%. The age at presentation was 3 to 23 years. Motor symptoms occurred in 72% (52 of 72 patients); palsies in Cranial Nerves IX, X, and XII in 33% (24 of 72 patients); and vertebrobasilar symptoms in 25% (18 of 72 patients). Trauma precipitated symptoms in 55% (40 of 72 patients). The best definition of the abnormality was demonstrated by 3-dimensional computed tomography combined with magnetic resonance imaging. Treatment was aimed at decompression of the pathology and stabilization.
Remnants of the occipital vertebrae around the foramen magnum were recognized in 72 of 5200 CVJ cases (7.2%). Magnetic resonance imaging with 3-dimensional computed tomography of the CVJ provides the best definition and understanding of the lesions. Brainstem myelopathy and lower cranial nerve deficits are common clinical presentations in the first and second decades of life. Treatment is aimed at decompression of the pathology and CVJ stabilization.
枕骨大孔周围的发育残余物,即原寰椎节段异常,在尸检研究中已有记录,但在临床环境中极为罕见。由于其罕见性,病理解剖结构一直被误解,治疗也充满失败。这项前瞻性研究的目的是了解相关的解剖学、病理学和胚胎学,识别临床表现,并深入了解治疗和管理方法。
我们的颅颈交界区(CVJ)数据库始于1977年,包含5200例病例。这项前瞻性研究具有检索功能。神经诊断研究随着影像学的发展而变化。72例患者被确诊为有症状的原寰椎节段异常。
斜坡或枕骨内侧髁的腹侧骨质肿块占66%(44/72),外侧或前外侧压迫性肿块占37%(72例患者中的27例),背侧骨质压迫占17%(72例患者中的12例)。33%的患者伴有后脑疝。发病年龄为3至23岁。72%(52/72)的患者出现运动症状;33%(24/72)的患者出现第九、十和十二对颅神经麻痹;25%(18/72)的患者出现椎基底动脉症状。55%(40/72)的患者症状由外伤诱发。三维计算机断层扫描结合磁共振成像能最好地显示异常情况。治疗旨在解除病变压迫并实现稳定。
在5200例CVJ病例中,有72例(7.2%)发现枕骨大孔周围存在枕椎残余物。CVJ的磁共振成像结合三维计算机断层扫描能对病变提供最佳的显示和理解。脑干脊髓病和下颅神经功能缺损是10至20岁年龄段常见的临床表现。治疗旨在解除病变压迫并稳定CVJ。