Endoscopic Management of Spontaneous Clival Cerebrospinal Fluid Leaks: Case Series and Literature Review

2016 ◽  
Vol 86 ◽  
pp. 470-477 ◽  
Author(s):  
Fabio Pagella ◽  
Alessandro Pusateri ◽  
Elina Matti ◽  
Cesare Zoia ◽  
Marco Benazzo ◽  
...  
Author(s):  
Ricardo L. Carrau ◽  
Allan D. Vescan ◽  
Carl H. Snyderman ◽  
Amin B. Kassam

2020 ◽  
Vol 5 (3) ◽  
pp. 375-380
Author(s):  
Alice Z. Maxfield ◽  
Sarina K. Mueller ◽  
Aaishah R. Raquib ◽  
Ahmad R. Sedaghat ◽  
Regan W. Bergmark ◽  
...  

2014 ◽  
Vol 21 (5) ◽  
pp. 805-810 ◽  
Author(s):  
Frank Mihlon ◽  
Peter G. Kranz ◽  
Andreia Roxana Gafton ◽  
Linda Gray

Object Cerebrospinal fluid leaks due to unrecognized durotomy during spinal surgery are often managed with a second surgery for dural closure. CT-guided percutaneous patching targeted to the dural defect offers an alternative to surgery since it can be performed in a minimally invasive fashion without the need for general anesthesia. This case series describes the authors' experience using targeted CT-guided percutaneous patching to repair incidental durotomies incurred during spinal surgery. Methods This investigation is a retrospective case series involving patients who underwent CT-guided percutaneous patching of surgical incidental durotomies and were referred between January 2007 and June 2013. Their presenting clinical history, myelographic findings, and clinical outcomes, including the need for eventual surgical duraplasty, were reviewed. Results Nine cases were identified, including 7 durotomies incurred during lumbar discectomy, one due to a medial transpedicular screw breach, and one incurred during vertebrectomy for spinal osteosarcoma. All patients who had favorable outcomes with percutaneous intervention alone had 2 common features: dural defect of 4 mm or smaller and absence of a pseudomeningocele. Patients with CSF leaks complicated by pseudomeningocele and those with a dural defect of 6 mm or more all required eventual surgical management. Conclusions The authors' results suggest that findings on CT myelography may help predict which patients with postsurgical durotomy can be treated with percutaneous intervention. In particular, CT-guided patching may be more likely to be successful in those patients with dural defects of less than 5 mm and without pseudomeningocele. In patients with larger dural defects or pseudomeningoceles, percutaneous blood patching alone is unlikely to be successful.


2006 ◽  
Vol 66 (4) ◽  
pp. 371-376 ◽  
Author(s):  
Joshua R. Dusick ◽  
Carlos A. Mattozo ◽  
Felice Esposito ◽  
Daniel F. Kelly

2009 ◽  
Vol 25 (01) ◽  
pp. 029-037 ◽  
Author(s):  
J. Sanderson ◽  
Stilianos Kountakis ◽  
K. McMains

Author(s):  
Kristen L. Yancey ◽  
Nauman F. Manzoor ◽  
Robert J. Yawn ◽  
Matthew O'Malley ◽  
Alejandro Rivas ◽  
...  

Abstract Objectives The main purpose of this article is to investigate the prevalence and features of posterior fossa defects (PFD) in spontaneous cerebrospinal fluid leaks (sCSFL). Design Retrospective case series. Setting Tertiary skull base center. Participants Consecutive adults undergoing lateral skull base repair of sCSFL between 2003 and 2018. Main Outcome Measures The following data were collected: demographics, comorbidities, radiology and intraoperative findings, and surgical outcomes including complications and need for revision surgery or shunt placement. Patients with incomplete data or leaks following skull base surgery, trauma, or chronic ear disease were excluded. Results Seventy-one patients (74% female, mean age 56.39 ± 11.50 years) underwent repair of spontaneous lateral skull base leaks. Eight ears (7 patients, 11.1%) had leaks involving the posterior fossa plate in addition to defects of the tegmen mastoideum (50%), tegmen tympani (25%), or both (25%). Patients with PFDs more often had bilateral tegmen thinning on imaging (75%, odds ratio [OR]: 10.71, 95% confidence interval [CI]: 2.20–54.35, p = 0.005) and symptomatic bilateral leaks (OR: 9.67, 95% CI: 2.22–40.17, p = 0.01. All PFD patients had arachnoid granulations adjacent to ipsilateral mastoid cell opacification. However, this finding was often subtle and rarely included on the radiology report. There was no significant difference in body mass index, age, presenting complaints, or operative success between the PFD and isolated tegmen defect sCSFL cohorts. Conclusions The posterior fossa is an uncommon location for sCSFL. Careful review of preoperative imaging is often suggestive and can inform surgical approach. PFD patients are similar to those with isolated tegmen-based defects in presentation, comorbidities, and outcomes.


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