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Management of multiple spontaneous nasal meningoencephaloceles.

机译:多发性自发性鼻脑膜脑膨出的处理。

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OBJECTIVES/HYPOTHESIS: Multiple spontaneous nasal meningoencephaloceles in the same patient are rare lesions. Although many skull base defects occur after prior trauma or surgery, otolaryngologists must be aware of the potential for spontaneous encephaloceles. We present our experience with this unusual condition and discuss its pathophysiology and unique management issues. STUDY DESIGN: Retrospective. METHODS: Review of medical records, radiographic images, and cerebrospinal fluid pressures. RESULTS: We identified 5 patients with multiple, simultaneous, spontaneous encephaloceles: 4 patients with 2 encephaloceles and 1 patient with 3 encephaloceles (11 in all). Locations of the 11 encephaloceles were sphenoid lateral recess (6), frontal sinus with supraorbital ethmoid extension (2), ethmoid roof (1), frontal sinus (1), and central sphenoid (1). Three patients had bilateral sphenoid lateral recess encephaloceles, accounting for all six in that location. All four patients with available radiographic studies demonstrated empty sella turcica. Surgical approaches included endoscopic transpterygoid approach to the lateral sphenoid recess (3), endoscopic approach to ethmoid and central sphenoid (3), and osteoplastic flap with frontal sinus obliteration (2). We had 100% success at latest endoscopic follow-up (mean period, 17 mo). Three patients had postoperative lumbar punctures with mean cerebrospinal fluid pressure of 28.3 cm water (range, 19-34 cm; normal range, 0-15 cm). Conclusions: Multiple spontaneous encephaloceles can be managed safely and successfully using endoscopic and extracranial approaches. A high index of suspicion for this diagnosis must be maintained, especially in patients with radiographic evidence of laterally pneumatized sphenoid sinuses or empty sella. Spontaneous encephaloceles and cerebrospinal fluid leaks represent a form of intracranial hypertension.
机译:目的/假设:同一患者中多发性自发性鼻脑膜脑膨出是罕见病灶。尽管许多颅骨基部缺损是在先前的创伤或手术后发生的,但耳鼻喉科医生必须意识到自发性脑膨出的可能性。我们将介绍这种异常情况的经验,并讨论其病理生理学和独特的管理问题。研究设计:回顾性研究。方法:审查病历,X射线图像和脑脊液压力。结果:我们确定了5例同时发生多发性自发性脑膨出的患者:4例具有2例脑膨出和1例具有3例脑膨出(共11例)。 11个脑膨出的位置是蝶骨外侧隐窝(6),眶上筛骨延长的额窦(2),筛窦顶(1),额窦(1)和中央蝶骨(1)。三例患者有双侧蝶骨外侧隐窝性脑膨出,占该部位的全部六个。接受放射学检查的所有四名患者均显示出空的蝶鞍。手术方法包括内镜下蝶骨入路到外侧蝶骨隐窝(3),内镜下筛骨到筛窦和中央蝶骨(3),以及具有额窦闭塞的骨塑皮瓣(2)。在最近的内镜随访中(平均周期为17个月),我们获得了100%的成功。三例患者术后腰椎穿刺,平均脑脊液压力为28.3 cm水(范围19-34 cm;正常范围0-15 cm)。结论:使用内窥镜和颅外方法可以安全,成功地治疗多发性自发性脑膨出。对于这种诊断,必须保持高度怀疑,特别是在有X线影像显示蝶状气窦或空蝶鞍的患者中。自发性脑膨出和脑脊液漏代表颅内高压的一种形式。

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