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颅底隐匿性畸形。

Occult malformations of the skull base.

作者信息

Schick B, Draf W, Kahle G, Weber R, Wallenfang T

机构信息

Department of Otolaryngology, Head and Neck Surgery, Plastic Facial Surgery and Communication Disorders, Hospital Fulda, Academic Teaching Hospital of the University of Marburg, Fulda, Germany.

出版信息

Arch Otolaryngol Head Neck Surg. 1997 Jan;123(1):77-80. doi: 10.1001/archotol.1997.01900010087013.

Abstract

Occult malformations of the skull base are rare anomalies. They are often not detected until they give rise to complications such as meningitis or cerebrospinal fluid rhinorrhea. We used high-resolution computed tomography, fluorescein endoscopy, cisternography, magnetic resonance imaging, and duraplasty to diagnose occult malformations of the skull base in 4 patients. The four patients had had between 4 and 6 attacks of meningitis. Cerebrospinal fluid rhinorrhea was confirmed in 3 cases. The following occult malformations were found: (1) an encephalocele of the glabella/cribriform plate and a meningocele at the petrous bone apex, (2) a meningoencephalocele at the petrous bone apex, (3) dural lesions in the regions foramen rotundum/sphenoid sinus and frontal sinus/cribriform plate, and (4) a dural lesion of the sphenoid sinus. In patients presenting with recurrent meningitis, meningitis with isolation of upper airway pathogens, or cerebrospinal fluid rhinorrhea, modern diagnostic methods should be used to search for dural lesions. Diagnosis of an occult malformation makes it possible to perform the necessary surgical repair and thus prevent the further occurrence of potentially fatal episodes of meningitis.

摘要

颅底隐匿性畸形是罕见的异常情况。它们通常在引发脑膜炎或脑脊液鼻漏等并发症之前不会被发现。我们使用高分辨率计算机断层扫描、荧光素内镜检查、脑池造影、磁共振成像和硬脑膜成形术对4例患者的颅底隐匿性畸形进行诊断。这4例患者曾有过4至6次脑膜炎发作。3例确诊为脑脊液鼻漏。发现了以下隐匿性畸形:(1)眉间/筛板脑膨出和岩骨尖脑膜膨出,(2)岩骨尖脑膜脑膨出,(3)圆孔/蝶窦和额窦/筛板区域的硬脑膜病变,以及(4)蝶窦硬脑膜病变。对于出现复发性脑膜炎、分离出上呼吸道病原体的脑膜炎或脑脊液鼻漏的患者,应采用现代诊断方法来寻找硬脑膜病变。隐匿性畸形的诊断使得进行必要的手术修复成为可能,从而预防可能致命的脑膜炎发作的进一步发生。

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