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累及颞骨的骨硬化症:临床与影像学表现

Sclerosteosis involving the temporal bone: clinical and radiologic aspects.

作者信息

Nager G T, Stein S A, Dorst J P, Holliday M J, Kennedy D W, Diehn K W, Jabs E W

出版信息

Am J Otolaryngol. 1983 Jan-Feb;4(1):1-17. doi: 10.1016/s0196-0709(83)80002-7.

Abstract

Sclerosteosis is one of the rare, potentially lethal, autosomal recessive, progressive, craniotubular sclerosing bone dysplasias. Syndactyly of the second and third or other fingers is evident at birth. Hyperostosis and sclerosis are most prominent in the skull and tubular bones, and are frequently associated with excessive height and weight. The typical facial deformity is apparent by the age of 5 years. The changes involving the temporal bone include a marked increase in overall dimensions, extreme sclerosis, and narrowing and constriction of the external ear canal, middle ear cleft, internal acoustic meatus, and falloppian canal. Impairment of hearing, as a rule bilateral, is a frequent presenting symptom which may manifest in early childhood. Initially it is an expression of interference with sound conduction; later it may become associated with a loss of sound perception. Impairment of facial nerve function is another salient feature which occasionally is present at birth. As a rule, it manifests initially as a unilateral, recurrent paresis, eventually progressing to a bilateral permanent partial loss of facial nerve function. Since impairments of hearing and facial nerve function are two of the salient features, present at birth or in early childhood, the responsibility for recognizing the disease often falls upon the otolaryngologist. The clinical and radiologic features permit not only early recognition of the disorder but also differentiation from similar bony dysplasias. Hyperosteosis and sclerosis of the skull lead to thickening and distortion of the calvaria, cranial base, and foramen magnum resulting in reduction of the intracranial volume, interference with the cerebral blood flow, resorption of cerebrospinal fluid, and gradual increase of intracranial pressure. Severe headaches resulting from this mechanism often develop in early adulthood, and several patients have died suddenly from impaction of the medulla oblongata in the foramen magnum. Decompression of the transverse sigmoid sinus and jugular bulb may be lifesaving, combined with a posterior, and if necessary, an anterior, craniectomy for decompression. Early decompression of the internal acoustic meatus and falloppian canal may help in the preservation of cochlear and facial nerve function.

摘要

骨硬化症是一种罕见的、具有潜在致命性的常染色体隐性进行性颅管硬化性骨发育异常疾病。出生时可见第二和第三或其他手指并指。骨质增生和硬化在颅骨和管状骨中最为明显,且常与身高和体重超标有关。典型的面部畸形在5岁时明显可见。颞骨的改变包括整体尺寸显著增加、极度硬化以及外耳道、中耳裂、内耳道和面神经管变窄和狭窄。听力障碍通常为双侧,是常见的首发症状,可能在儿童早期出现。起初它是声音传导受干扰的表现;后来可能与声音感知丧失有关。面神经功能障碍是另一个显著特征,偶尔在出生时就存在。通常,它最初表现为单侧、复发性轻瘫,最终发展为双侧永久性面神经功能部分丧失。由于听力和面神经功能障碍是出生时或儿童早期的两个显著特征,因此识别该疾病的责任往往落在耳鼻喉科医生身上。临床和放射学特征不仅有助于早期识别该疾病,还能与类似的骨发育异常进行鉴别。颅骨的骨质增生和硬化导致颅盖、颅底和枕大孔增厚和变形,导致颅内体积减小、脑血流受干扰、脑脊液吸收以及颅内压逐渐升高。由此机制引起的严重头痛常在成年早期出现,一些患者因延髓在枕大孔受压而突然死亡。横窦乙状窦和颈静脉球减压可能挽救生命,同时进行后颅窝开颅减压,必要时进行前颅窝开颅减压。内耳道和面神经管的早期减压可能有助于保留耳蜗和面神经功能。

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