scholarly journals Cranial Nerve Preservation in Surgery for Large Acoustic Neuromas

Skull Base ◽  
2004 ◽  
Vol 14 (2) ◽  
pp. 85-90 ◽  
Author(s):  
J. Thomas Roland ◽  
Andrew J Fishman ◽  
John G Golfinos ◽  
Noel Cohen ◽  
George Alexiades ◽  
...  
1991 ◽  
Vol 105 (5) ◽  
pp. 687-693 ◽  
Author(s):  
C. Gary Jackson ◽  
Roberto A. Cueva ◽  
Britt A. Thedinger ◽  
Michael E. Glasscock

Neurosurgery ◽  
2007 ◽  
Vol 61 (1) ◽  
pp. 76-81 ◽  
Author(s):  
Juan J. Martin ◽  
Douglas Kondziolka ◽  
John C. Flickinger ◽  
David Mathieu ◽  
Ajay Niranjan ◽  
...  

Abstract OBJECTIVE Jugular foramen region schwannomas are rare intracranial tumors that usually present with multiple lower cranial nerve deficits. For some patients, complete surgical resection is possible but may be associated with significant morbidity. Stereotactic radiosurgery is a minimally invasive alternative or adjunct to microsurgery for such tumors. We reviewed our clinical and imaging outcomes after patients underwent gamma knife radiosurgery for management of jugular foramen schwannomas. METHODS Thirty-four patients with 35 tumors (one patient had bilateral tumors) underwent radiosurgery between May 1990 and December 2005. Twenty-two patients had previous microsurgical resection and all patients experienced various cranial neuropathies. A median of six isocenters were used. Median marginal and maximum doses were 14 and 28 Gy, respectively. RESULTS None of the patients were lost to evaluation and the mean duration of follow-up was 83 months. Tumors regressed in 17 patients, remained stable in 16, and progressed in two. Five- and 10-year actuarial control rates were 97 and 94%, respectively. Preexisting cranial neuropathies improved in 20% and remained stable in 77% after radiosurgery. One patient worsened. The function of all previous intact nerves was preserved after radiosurgery. CONCLUSION Stereotactic radiosurgery proved to be a safe and effective management for newly diagnosed or residual jugular foramen schwannomas. Long-term tumor control rates and stability or improvement in cranial nerve function was confirmed.


Author(s):  
Frank Unger ◽  
C. Walch ◽  
O. Schröttner ◽  
S. Eustacchio ◽  
B. Sutter ◽  
...  

Neurosurgery ◽  
2012 ◽  
Vol 72 (1) ◽  
pp. 42-46 ◽  
Author(s):  
Cara L. Sedney ◽  
Yoichi Nonaka ◽  
Ketan R. Bulsara ◽  
Takanori Fukushima

Abstract BACKGROUND: Jugular foramen schwannomas are uncommon and surgically challenging lesions. OBJECTIVE: To determine the importance of surgical technique on morbidity and recurrence of jugular foramen schwannomas. METHODS: A retrospective review and case-control analysis of a single-senior-surgeon series of 81 patients with surgically treated jugular foramen schwannomas was performed, focusing on operative technique. Patients undergoing an aggressive, total tumor resection (series 1) were compared with those undergoing more conservative resection focusing on preserving the pars nervosa (series 2). RESULTS: There was a statistically significant (P = .04) decrease in permanent deficits of the cranial nerve 9/10 complex with a conservative technique. Recurrence was seen in 3 patients (5.7%) in series 1 and in 3 patients (10.7%) in series 2 (P = .36). Recurrence was treated with reoperation in 1 patient, radiation in 1 patient, and observation in the others. CONCLUSION: Although radical gross total resection is desirable, it is not optimal for cranial nerve preservation in patients with jugular foramen schwannomas. A more conservative approach resulted in a statistically significant decrease in lower cranial nerve deficits. There was a nonstatistically significant trend toward increasing recurrence, which may be treated with multiple modality therapy in the modern era.


1995 ◽  
Vol 52 (1) ◽  
pp. 73-79 ◽  
Author(s):  
O. K. Ogunrinde ◽  
L. D. Lunsford ◽  
J. C. Flickinger ◽  
D. S. Kondziolka

1995 ◽  
Vol 64 (1) ◽  
pp. 87-97 ◽  
Author(s):  
O.K. Ogunrinde ◽  
D.L. Lunsford ◽  
D.S. Kondziolka ◽  
D.J. Bissonette ◽  
J.C. Flickinger

2018 ◽  
Vol 20 (2) ◽  
pp. 169-182
Author(s):  
Michael T. Selch  

Stereotactic cerebral irradiation is a radiotherapeutic technique for precise delivery of ionizing irradiation to an intracranial target with simultaneous sparing of adjacent parenchyma. Treatment can be administered by a multi-source cobalt-60 device (gamma knife) or a dedicated linear accelerator.The target dose can be delivered in a large, single fraction (stereotactic radiosurgery SRS) or in multiple, daily increments (stereotactic radiotherapy SRT). The latter approach combines the physical dose localization advantages of SRS with the radiobiologic benefits of dose fractionation. This literature review will present the rationale and clinical results of SRS and SRT for the treatment of acoustic neuromas. Emphasis will be placed on tumor control, imaging outcome and cranial nerve preservation. The findings demonstrate that SRS and SRT represent reasonable therapeutic options for patients with acoustic neuromas.


2020 ◽  
Vol 162 (6) ◽  
pp. 897-904
Author(s):  
Anne K. Maxwell ◽  
Gautam U. Mehta ◽  
Thomas Muelleman ◽  
Zachary R. Barnard ◽  
Thomas Hartwick ◽  
...  

Objective To provide the first description of hypofractionated stereotactic radiosurgery (SRS) and evaluate tumor control and safety for vagal paragangliomas (VPs), which begin at the skull base but often have significant extracranial extension. Study Design Retrospective chart review. Setting Tertiary-referral neurotology and neurosurgery practice. Subjects and Methods Five VPs in 4 patients (all male, ages 15-56 years) underwent SRS between 2010 and 2018. Outcome measures included tumor dimensions on serial imaging, cranial nerve function, and radiation side effects. Results CyberKnife hypofractionated SRS was performed. The prescription dose was 24 or 27 Gy (maximum dose 33.4 Gy; range, 29.3-35.5 Gy) delivered in 3 equal fractions. The mean isodose line was 79% (range, 76%-82%). Four VPs were treated primarily, and 1 tumor underwent SRS to treat regrowth 2 years after microsurgical subtotal resection via the modified infratemporal fossa approach. The treatment volume ranged from 8.81 to 86.3 cm3 (mean, 35.7 cm3). All demonstrated stable size (n = 3) or regression (n = 2) at last follow-up, 63 to 85 months after SRS (mean, 76 months). One patient had stable premorbid vocal fold paralysis from a prior ipsilateral glomus jugulare tumor resection. All others demonstrated normal vagal function following SRS. Treatment-related side effects, including dysgeusia (n = 1), mucositis (n = 1), and neck soft-tissue edema (n = 2), were self-limited. Conclusions Hypofractionated SRS appears to be both safe and effective for treating VPs, including large-volume and predominantly extracranial tumors, while preserving vagal function. SRS should be considered as a cranial nerve preservation option, especially in settings of contralateral lower cranial nerve deficits or in those with multiple paragangliomas risking both vagal nerves.


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