成人1型Chiari畸形。

Athanasios Zisakis, Rosa Sun, Joshua Pepper, Georgios Tsermoulas
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引用次数: 1

摘要

术语Chiari畸形是指颅椎交界处的一组异质解剖异常。Chiari畸形1型(CM1)是指小脑扁桃体通过枕骨大孔异常突出,是迄今为止最常见的类型。其患病率估计约为1%;它在女性中更为常见,在25-70%的病例中与脊髓空洞有关。流行的病理生理学理论提出,小后颅窝和正常发育的后脑之间的形态不匹配导致扁桃体异位。在大多数人中,CM1是无症状的,是偶然诊断出来的。在有症状的病例中,头痛是主要症状。典型的头痛是由瓦尔萨瓦式的动作引起的。许多其他症状是非特异性的,在没有脊髓空洞的情况下,自然病史是良性的。脊髓空洞症表现为不同程度的脊髓功能障碍。CM1患者的治疗方法应该是多学科的,治疗的第一步是对症状进行表型分析,因为它们可能是由其他病理引起的,如原发性头痛综合征。磁共振成像显示枕骨大孔以下5毫米或更多的小脑扁桃体是金标准的检查方式。诊断检查可能包括颅颈交界处的动态成像和颅内压监测。CM1的管理是可变的,有时是有争议的。手术通常用于头痛致残性或因鼻咽引起的神经功能缺损的患者。颅颈交界处的手术减压是应用最广泛的手术。已经提出了几种手术技术,但由于缺乏高质量的证据,在最佳治疗策略上没有达成共识。妊娠期的病情管理,限制与运动相关的生活方式,以及过度活动的共存需要特别考虑。
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Chiari Malformation Type 1 in Adults.

The term Chiari malformation refers to a heterogeneous group of anatomical abnormalities at the craniovertebral junction. Chiari malformation type 1 (CM1) refers to the abnormal protrusion of cerebellar tonsils through the foramen magnum and is by far the commonest type. Its prevalence is estimated approximately 1%; it is more common in women and is associated with syringomyelia in 25-70% of cases. The prevalent pathophysiological theory proposes a morphological mismatch between a small posterior cranial fossa and a normally developed hindbrain that results in ectopia of the tonsils.In most people, CM1 is asymptomatic and diagnosed incidentally. In symptomatic cases, headache is the cardinal symptom. The typical headache is induced by Valsalva-like maneuvers. Many of the other symptoms are nonspecific, and in the absence of syringomyelia, the natural history is benign. Syringomyelia manifests with spinal cord dysfunction of varying severity. The approach to patients with CM1 should be multidisciplinary, and the first step in the management is phenotyping the symptoms, because they may be due to other pathologies, like a primary headache syndrome. Magnetic resonance imaging, which shows cerebellar tonsillar decent 5 mm or more below the foramen magnum, is the gold standard investigative modality. The diagnostic workup may include dynamic imaging of the craniocervical junction and intracranial pressure monitoring.The management of CM1 is variable and sometimes controversial. Surgery is usually reserved for patients with disabling headaches or neurological deficits from the syrinx. Surgical decompression of the craniocervical junction is the most widely used procedure. Several surgical techniques have been proposed, but there is no consensus on the best treatment strategy, mainly due to lack of high-quality evidence. The management of the condition during pregnancy, restriction to lifestyle related to athletic activities, and the coexistence of hypermobility require special considerations.

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