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脑脊液耳漏

Cerebrospinal fluid otorrhea.

作者信息

Hicks G W, Wright J W, Wright J W

出版信息

Laryngoscope. 1980 Nov;90(11 Pt 2 Suppl 25):1-25. doi: 10.1288/00005537-198011001-00001.

Abstract

Cerebrospinal fluid (CSF) otorrhea is a dangerous and potentially life threatening occurrence for which the otolaryngologist is often consulted. CSF otorrhea occurs on the basis of skull fracture, tumor, infections, congenital anomalies, and operative trauma. Forty-three patients with CSF otorrhea of varied etiology are reviewed in this paper. Eight cases are of congenital or labyrinthine origin confirming at surgery the probable connection between the subarachnoid and perilymphatic spaces. Eleven cases had spinal fluid otorrhea due to infection. All cases presented with symptoms of chronic infection: 4 cases had a history of previous surgery for chronic ear disease; 7 cases had temporal lobe abscess; 1 case had a cerebellar abscess; 8 had tegmen defects secondary to cholesteatoma; in 1 case the tegmen defect was due to previous surgery for chronic infection. Nine of 11 cases have serviceable hearing postoperatively. Fourteen cases of spinal fluid otorrhea resulted from trauma: 1 case was due to traumatic stapes footplate fracture in a congenitally malformed ear; 4 were due to transverse temporal bone fracture; and 9 were due to longitudinal temporal bone fractures. All transverse fractures resulted in nonhearing ears. Three cases were due to a combination of temporal bone fracture and infection. In 2 of these cases chronic infection preceded the fracture; in 1 case the fracture led to chronic ear disease with spinal fluid leakage. One patient required 1 surgical procedure for closure of the otorrhea, 1 patient 2 procedures, and 1 patient 3 procedures. Ten cases are due to translabyrinthine acoustic neuroma removal: 7 cases had resolution of the spinal fluid leakage after conservative nonsurgical treatment; and 3 required surgical intervention using muscle, fat and fascia obliteration of the spinal fluid pathway.

摘要

脑脊液耳漏是一种危险且可能危及生命的情况,耳鼻喉科医生经常会因此被咨询。脑脊液耳漏基于颅骨骨折、肿瘤、感染、先天性异常及手术创伤而发生。本文回顾了43例病因各异的脑脊液耳漏患者。8例为先天性或迷路源性,手术证实蛛网膜下腔与外淋巴间隙之间可能存在联系。11例脑脊液耳漏由感染引起。所有病例均有慢性感染症状:4例有慢性耳部疾病既往手术史;7例有颞叶脓肿;1例有小脑脓肿;8例有胆脂瘤继发的鼓室盖缺损;1例鼓室盖缺损是由于既往慢性感染手术所致。11例中有9例术后听力尚可。14例脑脊液耳漏由创伤引起:1例因先天性畸形耳的外伤性镫骨足板骨折;4例因颞骨横行骨折;9例因颞骨纵行骨折。所有横行骨折均导致患耳失聪。3例是颞骨骨折与感染共同所致。其中2例慢性感染先于骨折;1例骨折导致慢性耳部疾病伴脑脊液漏。1例患者耳漏闭合需1次手术,1例需2次手术,1例需3次手术。10例是由于经迷路入路切除听神经瘤:7例经保守非手术治疗后脑脊液漏消失;3例需手术干预,采用肌肉、脂肪和筋膜封闭脑脊液通路。

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