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后脑慢性疝出

Chronic herniation of the hindbrain.

作者信息

Williams B

出版信息

Ann R Coll Surg Engl. 1981 Jan;63(1):9-17.

Abstract

Herniation of the hindbrain occurs when the lowest parts of the cerebellum and sometimes part of the medulla are moved downwards through the foramen magnum, a pressure difference acting across the foramen magnum moulding the tissues into a plug. It is suggested that the clinical course in both adults and babies with spina bifida may be explained by the hindbrain hernia acting as a valve.The term 'Chiari Type I deformity' is commonly used for an abnormality in which the tonsils and lowermost parts of the cerebellar hemispheres are prolapsed through a normal foramen magnum. Acute herniation may occur as a result of space-occupying lesions. Chronic herniation may be morphologically identical although it tends to be more severe. Sometimes it will produce few symptoms which often may be delayed so that the original causative lesion may not be apparent. Causes include bone softening, tumour, or previous meningitis. Birth injury is probably the commonest cause of the deformity, which presents clinically in adults.In infants with severe forms of spina bifida a hindbrain herniation is present. This abnormality may be called 'Chiari Type II deformity' or Arnold-Chiari deformity and is an intra-uterine abnormality in which the fourth ventricle and medulla are grotesquely herniated before they are properly developed and the foramen magnum is enlarged.The commonest clinical presentation of Chiari Type I deformity is syringomyelia, which is usually not diagnosed until adult life. Other presentations include syringobulbia, headache, oscillopsia, attacks of giddiness, lower cranial nerve palsies, and ataxia. Particularly characteristic are cough headache and cough syncope. Syringomyelia and syringobulbia in particular may be irreversible by the time they are diagnosed. Nevertheless, surgical decompression may be successful in relieving symptoms of headache, cough syncope, and long-tract compression; most cases of syringomyelia show some improvement and in others progression of the disease is arrested. Operative techniques for hindbrain herniation are discussed.Chiari Type II deformity is probably responsible for the progression of hydrocephalus after birth in the majority of babies with spina bifida. Measurement of pressure in the cerebrospinal fluid above and below the foramen magnum shows that intermittent pressure difference is commonly present at times of neurological deterioration. Surgical decompression of the hernia in adults allows correction of the valvular effect, which may be monitored by pressure measurements. In babies the associated hydrocephalus is usually so gross that it requires separate treatment, but pressure monitoring may be of value in assessing the state of the disease.

摘要

当小脑的最低部分,有时还有部分延髓通过枕骨大孔向下移位时,就会发生后脑疝,作用于枕骨大孔两侧的压力差将组织塑形成一个栓子。有人认为,患有脊柱裂的成人和婴儿的临床病程都可以用作为瓣膜的后脑疝来解释。术语“Chiari I型畸形”通常用于描述一种异常情况,即扁桃体和小脑半球的最下部通过正常的枕骨大孔脱垂。急性疝可能由占位性病变引起。慢性疝在形态上可能相同,尽管往往更严重。有时它只会产生很少的症状,而且这些症状通常会延迟出现,以至于最初的致病病变可能不明显。病因包括骨质软化、肿瘤或既往脑膜炎。出生时的损伤可能是这种畸形最常见的原因,在成人中出现临床症状。在患有严重脊柱裂的婴儿中存在后脑疝。这种异常情况可称为“Chiari II型畸形”或Arnold-Chiari畸形,是一种子宫内异常,其中第四脑室和延髓在正常发育之前就严重疝出,且枕骨大孔扩大。Chiari I型畸形最常见的临床表现是脊髓空洞症,通常直到成年才被诊断出来。其他表现包括延髓空洞症、头痛、视振荡、眩晕发作、下颅神经麻痹和共济失调。特别典型的是咳嗽性头痛和咳嗽性晕厥。脊髓空洞症和延髓空洞症尤其在被诊断时可能已不可逆转。然而,手术减压可能成功缓解头痛、咳嗽性晕厥和长束受压的症状;大多数脊髓空洞症病例会有一些改善,其他病例中疾病的进展会停止。文中讨论了后脑疝的手术技术。Chiari II型畸形可能是大多数患有脊柱裂的婴儿出生后脑积水进展的原因。测量枕骨大孔上方和下方脑脊液的压力表明,在神经功能恶化时通常存在间歇性压力差。对成人的疝进行手术减压可纠正瓣膜效应,这可通过压力测量来监测。在婴儿中,相关的脑积水通常非常严重,需要单独治疗,但压力监测可能有助于评估疾病状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed84/2493879/2dcc96ccac19/annrcse01504-0014-a.jpg

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