Challenges in the Management of Symptomatic Fallopian Canal Meningoceles: A Multicenter Case Series and Literature Review

Author:

Filip Peter1,Chiang Harry2,Goldberg Allison3,Khorsandi Azita S.4,Moonis Gul5,Moody Antonio Stephanie A.3,Wanna George1,Cosetti Maura

Affiliation:

1. Department of Otolaryngology—Head and Neck Surgery, The Mount Sinai Hospital

2. Columbia University Vagelos College of Physicians and Surgeons, New York, NY

3. Department of Otolaryngology, Eastern Virginia Medical School, Norfolk, VA

4. New York Eye and Ear of Mount Sinai

5. CUMC Division of Neuroradiology, Columbia University Medical Center, New York, NY

Abstract

Objective To describe the presentations, the diagnosis, our treatment approaches, and the outcomes for 11 patients with fallopian canal meningocele (FCM). Study Design: Multicenter Retrospective case series. Setting Tertiary referral centers. Patients Patients (N = 11) with radiographically or intraoperatively identified, symptomatic FCM. Interventions Surgical repair of cerebrospinal fluid (CSF) leak and meningocele versus observation. Main Outcome Measures Presentation (including symptoms, radiographic imaging, and comorbidities), management (including surgical approach, technique for packing, use of lumbar drain), clinical outcomes (control of CSF leak, meningitis, facial nerve function), and revision surgery. Results Patients presented with spontaneous CSF leak (n = 7), conductive (N = 11) and sensorineural hearing loss (n = 3), nonpositional intermittent vertigo (n = 3), headaches (n = 4), and recurrent meningitis (n = 1). Risk factors in our series included obesity (n = 4), Chiari 1 malformation (n = 1), and head trauma (n = 2). Noncontrast computed tomography of the temporal bone and magnetic resonance imaging were positive for FCM in 10 patients. Eight patients were managed surgically via a transmastoid approach (n = 4), combined transmastoid and middle fossa (N = 3), or middle fossa alone (n = 1); three were managed conservatively with observation. Postoperative complications included worsened facial nerve palsy (n = 1), recurrent meningitis (n = 1), and persistent CSF leak that necessitated revision (n = 1). Conclusions Facial nerve meningoceles are rare with variable presentation, often including CSF otorrhea. Management can be challenging and guided by symptomatology and comorbidities. Risk factors for FCM include obesity and head trauma, and Chiari 1 malformation may present with nonspecific otologic symptoms, in some cases, meningitis and facial palsy. Layered surgical repair leads to high rates of success; however, this may be complicated by worsening facial palsy.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference19 articles.

1. Fallopian canal meningocele: report of two cases;Otol Neurotol,2009

2. Cerebrospinal fluid otorrhea through a congenitally patent fallopian canal;Arch Otolaryngol,2000

3. Spontaneous CSF otorrhea caused by abnormal development of the facial nerve canal;AJNR Am J Neuroradiol,1999

4. Congenital cerebrospinal otorrhea;Ann Otol Rhinol Laryngol,1979

5. Spontaneous cerebrospinal fluid fistula through a congenitally patent facial nerve canal: incrimination of idiopathic intracranial hypertension;Otol Neurotol,2008

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