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1.
Auris Nasus Larynx ; 48(3): 383-393, 2021 Jun.
Article in English | MEDLINE | ID: mdl-32972774

ABSTRACT

OBJECTIVES: The study aimed at the analysis of the parameters of acoustic cervical and ocular vestibular evoked myogenic potentials (AC-cVEMP and AC-oVEMP) response in patients with a confirmed tumor located in the internal auditory canal. It also aimed to assess to what degree a combination of these tests may be of benefit in the preoperative indication of the affected nerve division via preoperative determination whether the tumor originated from the superior or inferior division of the vestibular nerve, both divisions, or if it originated from a different nerve in the internal auditory canal. METHODS: The study group included 50 patients. Preoperative MRI scans were used to measure tumor diameter. AC-cVEMP and AC-oVEMP testing were performed before tumor resection. The surgeon was asked for a detailed description of the tumor origin. RESULTS: The corrected amplitude of cVEMP was significantly lower on the tumor side than on the non-affected side and in the control group. The corrected Asymmetry Ratio (AR) of cVEMPs in patients with the tumor was significantly elevated above the reference values with the mean being 58.29% and the mean AR of oVEMPs in patients the tumor was 71.78% which made both results significantly higher than in the control group. Neither cVEMP nor oVEMP latency was significantly correlated with tumor size. Data obtained from cVEMP and oVEMP tests was an effective indicator of tumor origin in 74% of patients showing which division (or both divisions) of the VIIIth nerve was affected in comparison with information obtained from the surgeon. CONCLUSIONS: The combined use of AC-cVEMP and AC-oVEMP tests may be useful in surgical planning in patients the tumor located in the internal auditory canal, providing a highly probable determination of the division of the affected nerve. Such information is valuable for the surgeon as it offers additional knowledge about the tumor before the procedure. cVEMP and oVEMP results may not be used as the basis for the calculation of tumor size in patients.


Subject(s)
Acoustic Stimulation , Cochlear Nerve/physiopathology , Cranial Nerve Neoplasms/diagnosis , Vestibular Evoked Myogenic Potentials/physiology , Vestibular Nerve/physiopathology , Vestibulocochlear Nerve Diseases/diagnosis , Case-Control Studies , Cranial Nerve Neoplasms/physiopathology , Ear, Inner , Female , Humans , Male , Middle Aged , Prospective Studies , Vestibulocochlear Nerve Diseases/physiopathology
2.
J Int Adv Otol ; 15(3): 415-419, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31846922

ABSTRACT

OBJECTIVES: The aim of this study was to evaluate the preoperative and postoperative facial nerve (FN) function in patients with FN schwannoma (FNS) and analyze the duration of preoperative facial palsy according to the preoperative and postoperative facial function. MATERIALS AND METHODS: We retrospectively reviewed the medical records of 29 patients with FNS who underwent surgery. We evaluated the FN function according to the type of FN manipulation and location of the anastomoses in the cable nerve graft, and we also analyzed the duration of facial palsy according to the facial function before and after surgery. RESULTS: All 4 patients who underwent nerve-stripping surgery had the House-Brackmann (H-B) Grade III, 12 of 21 who underwent a cable nerve graft had the H-B Grade III or better postoperatively, and all 4 who underwent a hypoglossal facial crossover had the H-B Grade IV. Patients who underwent cable nerve grafting were more likely to have better FN function when the proximal anastomosis site was located in the internal auditory canal, geniculate ganglion, tympanic segment of FN, and distal end in the mastoid segment of FN. The duration of preoperative facial palsy was statistically shorter in patients with better postoperative facial function. CONCLUSION: Surgery can be considered in patients with FNS who have the H-B Grade III or worse. A shorter duration of facial palsy prior to surgery resulted in better postoperative facial function.


Subject(s)
Cranial Nerve Neoplasms/surgery , Facial Nerve/surgery , Facial Paralysis/surgery , Neurilemmoma/surgery , Adult , Cranial Nerve Neoplasms/complications , Cranial Nerve Neoplasms/physiopathology , Facial Nerve/physiopathology , Facial Paralysis/etiology , Facial Paralysis/physiopathology , Female , Humans , Male , Middle Aged , Neurilemmoma/complications , Neurilemmoma/physiopathology , Postoperative Period , Preoperative Period , Retrospective Studies , Treatment Outcome
3.
Laryngoscope ; 129(12): E434-E436, 2019 12.
Article in English | MEDLINE | ID: mdl-31211430

ABSTRACT

Vagal schwannomas are rare, benign tumors. Intermittent intraoperative neuromonitoring via selective stimulation of splayed motor fibers running on the schwannoma surface to elicit a compound muscle action potential has been previously reported as a method of preserving vagal motor fibers. In this case report, vagal sensory fibers are mapped and continuously monitored intraoperatively during high vagus schwannoma resection using the laryngeal adductor reflex (LAR). Mapping of nerve fibers on the schwannoma surface enabled identification of sensory fibers. Continuous LAR monitoring during schwannoma subcapsular microsurgical dissection enabled sensory (and motor) vagal fibers to be monitored in real time with excellent postoperative functional outcomes. Laryngoscope, 129:E434-E436, 2019.


Subject(s)
Cranial Nerve Neoplasms/surgery , Monitoring, Intraoperative/methods , Neurilemmoma/surgery , Vagus Nerve Diseases/surgery , Vagus Nerve , Cranial Nerve Neoplasms/diagnosis , Cranial Nerve Neoplasms/physiopathology , Female , Humans , Laryngoscopy , Magnetic Resonance Imaging , Middle Aged , Nerve Fibers/pathology , Neurilemmoma/physiopathology , Otorhinolaryngologic Surgical Procedures/methods , Vagus Nerve Diseases/diagnosis , Vagus Nerve Diseases/physiopathology
5.
Am J Otolaryngol ; 40(2): 236-246, 2019.
Article in English | MEDLINE | ID: mdl-30554886

ABSTRACT

Patients with vestibular schwannomas (VS) typically present with hearing loss and tinnitus as well as variable cranial nerve dysfunctions. Surgical resection, stereotactic radiotherapy and/or conservative management employing serial magnetic resonance or computed tomography imaging serve as the main treatment options. Quality of life (QoL) may be impacted by the extent of tumour burden and exacerbated or relieved by treatment. Subjective assessment and quality of life inventories provide valuable information in client centered approaches with important implications for treatment. The intention of QoL measurements affecting VS patients within a clinical setting is to facilitate discussions regarding treatment options and objectively evaluate patient- centered clinical outcomes in a naturalistic setting.


Subject(s)
Cranial Nerve Neoplasms/physiopathology , Cranial Nerve Neoplasms/therapy , Neuroma, Acoustic/physiopathology , Neuroma, Acoustic/therapy , Quality of Life , Vestibulocochlear Nerve Diseases/physiopathology , Vestibulocochlear Nerve Diseases/therapy , Adult , Conservative Treatment , Cranial Nerve Neoplasms/diagnosis , Cranial Nerve Neoplasms/psychology , Female , Hearing , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neuroma, Acoustic/diagnosis , Neuroma, Acoustic/psychology , Otologic Surgical Procedures , Radiosurgery , Retrospective Studies , Surveys and Questionnaires , Tomography, X-Ray Computed , Vestibule, Labyrinth , Vestibulocochlear Nerve Diseases/diagnosis , Vestibulocochlear Nerve Diseases/psychology
6.
J Craniofac Surg ; 29(4): 1023-1025, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29521743

ABSTRACT

Neuroma pain can be severe, persistent, and treatment-resistant. Forehead and scalp anesthesia is troublesome for patients. Following an iatrogenic ablative injury to the right supraorbital nerve, with subsequent painful neuroma formation, a human cadaveric nerve allograft (AxoGen, Alachua, FL) was used to restore sensation of the right forehead and treat pain. At 1-year follow-up, the patient was pain-free, and protective sensation to the right forehead was recovered with comparable static and dynamic 2-point discrimination between the injured (20 mm, 12 mm respectively) and the normal side (15 mm, 10 mm respectively). This is the first reported case of using a cadaver nerve allograft for successful direct neurotization of the skin and restoration of sensation in the upper part of the face, and for treating painful neuromas. Moreover, a brief review of the available techniques for treating neuromas of the supraorbital and supratrochlear nerves is provided.


Subject(s)
Cranial Nerve Neoplasms , Forehead , Neuralgia , Neuroma , Trigeminal Nerve Diseases , Cranial Nerve Neoplasms/physiopathology , Cranial Nerve Neoplasms/surgery , Forehead/innervation , Forehead/surgery , Humans , Iatrogenic Disease , Male , Middle Aged , Neuralgia/physiopathology , Neuralgia/surgery , Neuroma/physiopathology , Neuroma/surgery , Peripheral Nerves/transplantation , Transplantation, Homologous , Trigeminal Nerve Diseases/physiopathology , Trigeminal Nerve Diseases/surgery
7.
J Am Acad Audiol ; 29(2): 187-191, 2018 02.
Article in English | MEDLINE | ID: mdl-29401065

ABSTRACT

BACKGROUND: Schwannoma of the hypoglossal nerve is rare. This case report documents an atypical abnormality of the cervical vestibular evoked myogenic potential (cVEMP) in a patient with schwannoma of the hypoglossal nerve. The observed abnormality was attributed to the proximity of the hypoglossal nerve to the spinal accessory nerve in the medullary cistern and base of the skull. PURPOSE: To report cVEMP abnormality in a patient with hypoglossal nerve schwannoma and provide an anatomical correlation for this abnormality. RESEARCH DESIGN: Case report. STUDY SAMPLE: A 44-yr-old woman. DATA COLLECTION: Pure-tone and speech audiometry, tympanometry, acoustic stapedial reflex, auditory brainstem response, and cVEMP testing were performed. RESULTS: The audiological test results were normal except for the absence of cVEMP on the lesion side (right). CONCLUSIONS: A cVEMP abnormality indicating a compromised spinal accessory nerve was observed in a patient with hypoglossal nerve schwannoma. This case report highlights the importance of recording cVEMP in relevant neurological conditions and provides clinical proof for the involvement of the spinal accessory nerve in the vestibulocollic reflex pathway.


Subject(s)
Cranial Nerve Neoplasms/physiopathology , Hypoglossal Nerve Diseases/physiopathology , Neurilemmoma/physiopathology , Vestibular Evoked Myogenic Potentials/physiology , Adult , Female , Humans
8.
Childs Nerv Syst ; 34(5): 983-986, 2018 05.
Article in English | MEDLINE | ID: mdl-29279963

ABSTRACT

INTRODUCTION: Here we are presenting a unique case of malignant triton tumor of the trigeminal nerve in a 4-year-old boy who presented with diplopia and ptosis. INTERVENTION: Near total excision of the tumor was performed, and adjuvant chemotherapy and radiotherapy were administered. RESULTS: The patient is in good health and has no evidence of clinical and radiological tumor recurrence for 22  months.


Subject(s)
Cranial Nerve Neoplasms/physiopathology , Cranial Nerve Neoplasms/therapy , Trigeminal Nerve Diseases/physiopathology , Trigeminal Nerve Diseases/therapy , Antineoplastic Agents/therapeutic use , Blepharoptosis/etiology , Child, Preschool , Diplopia/etiology , Humans , Male , Neurosurgical Procedures/methods , Radiotherapy/methods
9.
World Neurosurg ; 104: 883-899, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28465275

ABSTRACT

BACKGROUND: Limited or no literature exists identifying factors associated with functional nerve recovery in patients undergoing resection of sixth cranial nerve (CN VI) schwannomas. METHODS: A systematic review of literature was performed on CN VI schwannomas that were treated surgically. Synthesizing the findings pooled from the literature, we investigated associations of patient demographics and clinical characteristics with postsurgical CN VI functional recovery in multivariable regression models. In addition, we present the findings of an adolescent woman surgically managed for intracavernous CN VI schwannoma. Complete encasement of the cavernous segment of the internal carotid artery is unique to our case. RESULTS: We synthesized data of 32 patients from 29 studies, and our index case. Overall, the mean age of the patients was 44.0 ± 16.5 years, and approximately 52% (n = 17) were female. Most tumors were left-sided (n = 18; 54.5%), with an average size of 3.46 ± 1.71 cm. The most common location was cisternal (n = 11; 33%), followed by cavernous sinus (CS) proper (n = 9; 27%), cisterocavernous (n = 8; 24%), orbital (n = 4; 12%) and caverno-orbital (n = 1; 3%). CN VI recovery was reported in less than half the cohort (n = 14; 45%). Tumor extension in the CS was significantly associated with lesser likelihood (odds ratio [OR], 0.07; 95% confidence interval [CI], 0.01-0.98; P = 0.048) of postsurgical CN VI recovery. Although female gender (OR, 0.86; 95% CI, 0.07-10.09; P = 0.906), large tumor size (>2.5 cm) (OR, 0.45; 95% CI, 0.07-2.89; P = 0.397), and solid consistency (OR, 0.37; 95% CI, 0.03-4.19; P = 0.421) were associated with lesser odds for recovery, these were not statistically significant. Likewise, although gross total resection (OR, 6.28; 95% CI, 0.33-118.25; P = 0.220) was associated with higher odds of nerve recovery, the estimates were statistically insignificant. CONCLUSIONS: CS involvement is associated with lesser odds for functional nerve recovery in patients undergoing surgical resection for CN VI schwannoma.


Subject(s)
Abducens Nerve Diseases/physiopathology , Abducens Nerve Diseases/surgery , Abducens Nerve/physiopathology , Abducens Nerve/surgery , Cranial Nerve Neoplasms/physiopathology , Cranial Nerve Neoplasms/surgery , Neurilemmoma/physiopathology , Neurilemmoma/surgery , Postoperative Complications/physiopathology , Radiosurgery , Recovery of Function/physiology , Adolescent , Adult , Aged , Cavernous Sinus/physiopathology , Cavernous Sinus/surgery , Child , Female , Humans , Male , Middle Aged , Odds Ratio , Prognosis , Young Adult
10.
J Neurooncol ; 122(2): 313-20, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25567352

ABSTRACT

Neurofibromatosis type 2 (NF2) is a genetic disorder with bilateral vestibular schwannomas (VS) as the most frequent manifestation. Merlin, the NF2 tumor suppressor, was identified as a negative regulator of mammalian target of rapamycin complex 1. Pre-clinical data in mice showed that mTORC1 inhibition delayed growth of NF2-schwannomas. We conducted a prospective single-institution open-label phase II study to evaluate the effects of everolimus in ten NF2 patients with progressive VS. Drug activity was monitored every 3 months. Everolimus was administered orally for 12 months and, if the decrease in tumor volume was >20 % from baseline, treatment was continued for 12 additional months. Other patients stopped when completed 12 months of everolimus but were allowed to resume treatment when VS volume was >20 % during 1 year follow-up. Nine patients were evaluable. Safety was evaluated using CTCAE 3.0 criteria. After 12 months of everolimus, no reduction in volume ≥20 % was observed. Four patients had progressive disease, and five patients had stable disease with a median annual growth rate decreasing from 67 %/year before treatment to 0.5 %/year during treatment. In these patients, tumor growth resumed within 3-6 months after treatment discontinuation. Everolimus was then reintroduced and VS decreased by a median 6.8 % at 24 months. Time to tumor progression increased threefold from 4.2 months before treatment to > 12 months. Hearing was stable under treatment. The safety of everolimus was manageable. Although the primary endpoint was not reached, further studies are required to confirm the potential for stabilization of everolimus.


Subject(s)
Antineoplastic Agents/therapeutic use , Cranial Nerve Neoplasms/drug therapy , Everolimus/therapeutic use , Neurilemmoma/drug therapy , Neurofibromatosis 2/drug therapy , Vestibulocochlear Nerve Diseases/drug therapy , Adolescent , Adult , Antineoplastic Agents/adverse effects , Biomarkers, Tumor/metabolism , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/physiopathology , Disease Progression , Disease-Free Survival , Everolimus/adverse effects , Female , Follow-Up Studies , Humans , Male , Mechanistic Target of Rapamycin Complex 1 , Multiprotein Complexes/antagonists & inhibitors , Multiprotein Complexes/metabolism , Neurilemmoma/pathology , Neurilemmoma/physiopathology , Neurofibromatosis 2/pathology , Neurofibromatosis 2/physiopathology , Prospective Studies , TOR Serine-Threonine Kinases/antagonists & inhibitors , TOR Serine-Threonine Kinases/metabolism , Treatment Outcome , Tumor Burden , Vestibulocochlear Nerve Diseases/pathology , Vestibulocochlear Nerve Diseases/physiopathology , Young Adult
11.
Br J Neurosurg ; 29(2): 213-8, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25372896

ABSTRACT

OBJECTIVE: Facial nerve schwannomas (FNS) are rare tumors, and their appropriate management remains the subject of considerable debate. This report details the results of a series of patients with FNS treated with stereotactic radiosurgery (SRS) at the University of Virginia. METHODS: We performed a retrospective review of the clinical and imaging outcomes of 5 patients who underwent Gamma Knife RS (GKRS) for small-to-medium-sized (<5 mL) FNS at our institution. The study population consisted of 3 males and 2 females with a median age of 35 years. All patients presented with varying degrees of facial palsy and/or hearing dysfunction. Tumor volumes at GKRS ranged from 0.1 to 5 (median=0.8) mL. The median maximum radiosurgical dose and tumor margin dose were 24 Gy and 12 Gy, respectively. RESULTS: After a median follow-up period of 12 (range, 6-36) months, three tumors were radiographically smaller and two remained stable. Facial function improved in three patients, remained stable in one patient, and slightly declined from House-Brackmann grade I to II in one patient. Hearing function was preserved in three patients and deteriorated in two patients, one from Gardner-Robertson grade I to II and the other from serviceable hearing grade II to III. CONCLUSION: SRS appears to offer a reasonable rate of facial nerve preservation and tumor control for patients with small-to-medium-sized FNS. Considering the published outcomes achieved with resection, RS may be the preferred first-line treatment for these tumors.


Subject(s)
Cranial Nerve Neoplasms/surgery , Neurilemmoma/surgery , Neuroma, Acoustic/surgery , Radiosurgery , Adult , Aged , Cranial Nerve Neoplasms/physiopathology , Female , Hearing , Humans , Male , Middle Aged , Neurilemmoma/diagnosis , Neuroma, Acoustic/diagnosis , Radiosurgery/methods , Treatment Outcome
12.
Neuroreport ; 25(13): 1069-74, 2014 Sep 10.
Article in English | MEDLINE | ID: mdl-25055143

ABSTRACT

This study aimed to examine the contributions of brain-derived neurotrophic factor (BDNF) at the injury site toward neuroma formation and nerve regeneration after inferior alveolar nerve transection. Histological analysis confirmed neuroma formation at 2 weeks after complete transection of the inferior alveolar nerve. A local administration of an antibody to BDNF inhibited connective tissue proliferation at the injury site and promoted nerve fiber integrity. Fluorogold labeling showed a significantly higher number of labeled cells in the trigeminal ganglion in the anti-BDNF-treated group compared with the vehicle control group. In-situ hybridization histochemistry showed intense signals for tropomyosin receptor kinase B mRNA in the area of the injury site containing fibrous or granular tissue in the anti-BDNF-treated group. In contrast, these signals were close to the detection limit in the area of the perineurium in intact nerve trunks, indicating that the signals were expressed by fibroblasts within the connective tissue. These findings suggest that antagonization of endogenous BDNF induced by nerve injury reduces neuroma formation, without inhibiting damaged axon regeneration.


Subject(s)
Brain-Derived Neurotrophic Factor/metabolism , Cranial Nerve Neoplasms/physiopathology , Mandibular Nerve/physiopathology , Nerve Regeneration/physiology , Neuroma/physiopathology , Trigeminal Nerve Injuries/physiopathology , Animals , Antibodies/administration & dosage , Brain-Derived Neurotrophic Factor/immunology , Cranial Nerve Neoplasms/etiology , Cranial Nerve Neoplasms/pathology , Fibroblasts/pathology , Fibroblasts/physiology , In Situ Hybridization , Male , Mandibular Nerve/pathology , Neuroma/etiology , Neuroma/pathology , RNA, Messenger/metabolism , Random Allocation , Rats, Sprague-Dawley , Receptor, trkB/metabolism , Stilbamidines , Trigeminal Nerve Injuries/complications , Trigeminal Nerve Injuries/pathology
13.
Ear Nose Throat J ; 92(2): E1-2, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23460218

ABSTRACT

We present an unusual case in which a patient diagnosed as having otosclerosis on the basis of clinical and audiologic findings actually had a middle ear facial nerve schwannoma. To the best of our knowledge, this is the first reported case in English literature in which a facial nerve schwannoma presented with conductive deafness of gradual onset and absent stapedial reflex with a normally functioning facial nerve. We also include a review of the literature.


Subject(s)
Cranial Nerve Neoplasms/diagnosis , Cranial Nerve Neoplasms/physiopathology , Ear Neoplasms/diagnosis , Ear Neoplasms/physiopathology , Ear, Middle/physiopathology , Facial Nerve Diseases/diagnosis , Facial Nerve Diseases/physiopathology , Neurilemmoma/diagnosis , Neurilemmoma/physiopathology , Otosclerosis/diagnosis , Otosclerosis/physiopathology , Reflex, Abnormal/physiology , Reflex, Acoustic/physiology , Stapedius/physiopathology , Adult , Diagnosis, Differential , Humans , Image Interpretation, Computer-Assisted , Male , Tomography, X-Ray Computed
14.
J Neuroophthalmol ; 33(1): 66-8, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23235433

ABSTRACT

A 34-year-old woman presented with brainstem compression from a large third nerve schwannoma although third nerve function was intact. At surgery, preservation of the proximal third nerve was not possible. Because of preexisting amblyopia of the contralateral eye, an attempt was made to surgically reinnervate the affected third nerve. The fourth nerve was divided at its entry into the tentorium and anastomosed to the distal stump of the third nerve. Partial recovery of third function occurred over several months and is still present 6 years later. Successful long-term reinnervation of the third nerve by direct anastomosis with the fourth nerve may be useful when third repair is not possible.


Subject(s)
Cranial Nerve Neoplasms/surgery , Eye Movements/physiology , Eyelids/physiopathology , Neurilemmoma/surgery , Oculomotor Nerve Diseases/surgery , Trochlear Nerve/surgery , Adult , Anastomosis, Surgical , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/physiopathology , Decompression, Surgical , Female , Humans , Neurilemmoma/pathology , Neurilemmoma/physiopathology , Oculomotor Nerve Diseases/pathology , Oculomotor Nerve Diseases/physiopathology , Recovery of Function/physiology , Treatment Outcome
15.
World Neurosurg ; 79(5-6): 763-7, 2013.
Article in English | MEDLINE | ID: mdl-22484073

ABSTRACT

BACKGROUND: Geniculate neuralgia, although uncommon, can be a debilitating pathology. Unfortunately, a thorough review of this pain syndrome and the clinical anatomy, function, and pathology of its most commonly associated nerve, the nervus intermedius, is lacking in the literature. Therefore, the present study aimed to further elucidate the diagnosis of this pain syndrome and its surgical treatment based on a review of the literature. METHODS: Using standard search engines, the literature was evaluated for germane reports regarding the nervus intermedius and associated pathology. A summary of this body of literature is presented. RESULTS: Since 1968, only approximately 50 peer-reviewed reports have been published regarding the nervus intermedius. Most of these are single-case reports and in reference to geniculate neuralgia. No report was a review of the literature. CONCLUSIONS: Neuralgia involving the nervus intermedius is uncommon, but when present, can be life altering. Microvascular decompression may be effective as a treatment. Along its cisternal course, the nerve may be difficult to distinguish from the facial nerve. Based on case reports and small series, long-term pain control can be seen after nerve sectioning or microvascular decompression, but no prospective studies exist. Such studies are now necessary to shed light on the efficacy of surgical treatment of nervus intermedius neuralgia.


Subject(s)
Facial Nerve/pathology , Facial Nerve/surgery , Herpes Zoster Oticus/pathology , Herpes Zoster Oticus/surgery , Parasympathetic Fibers, Postganglionic/pathology , Parasympathetic Fibers, Postganglionic/surgery , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/physiopathology , Cranial Nerve Neoplasms/surgery , Ear Canal/innervation , Earache/pathology , Earache/physiopathology , Earache/surgery , Facial Nerve/physiopathology , Facial Nerve Diseases/pathology , Facial Nerve Diseases/physiopathology , Facial Nerve Diseases/surgery , Facial Pain/pathology , Facial Pain/physiopathology , Facial Pain/surgery , Herpes Zoster Oticus/diagnosis , Herpes Zoster Oticus/physiopathology , Humans , Lacrimal Apparatus/innervation , Microvascular Decompression Surgery/methods , Nose/innervation , Palate/innervation , Parasympathetic Fibers, Postganglionic/physiopathology , Skin/innervation , Tongue/innervation
17.
Otolaryngol Head Neck Surg ; 147(3): 525-30, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22565049

ABSTRACT

OBJECTIVES: Primary facial nerve tumors (FNTs) present in varying ways. In this study, the authors present their institutional experience with the management of facial nerve tumors, including their recommendations for available therapies such as observation, microsurgical decompression or removal, and stereotactic radiation. They emphasize the auditory and facial nerve function outcomes. STUDY DESIGN: Retrospective case review. SETTING: Tertiary referral center. SUBJECTS AND METHODS: Retrospective review of all cases of FNT seen at the authors' tertiary care academic medical center over a 10-year period (2002-2011). The clinical presentation, treatment modality, and outcome parameters of cochlear and facial nerve function were assessed. RESULTS: Twelve patients were identified. House-Brackmann grades on presentation were 4 grade I, 2 grade II, 2 grade III, 1 grade IV, and 3 grade V, with 2 grade V patients declining to grade VI shortly after presentation. Seven patients presented with serviceable hearing and 4 with nonserviceable hearing. Treatment options/arms included observation with serial clinicoradiological review (2 cases), stereotactic radiation with the CyberKnife (3 cases), wide fallopian canal decompression (3 cases), microsurgical excision and repair (3 cases), and biopsy followed by observation (1 case). At the end of the review period, facial nerve function was stable in 8 patients, improved in 3, and declined in 1, and none had documented worsening of hearing based on American Academy of Otolaryngology--Head and Neck Surgery Foundation classification. CONCLUSIONS: Management of FNT is largely based on the clinicoradiological picture. Each treatment arm is different, but overall auditory and facial function can be maintained.


Subject(s)
Cranial Nerve Neoplasms/surgery , Facial Nerve Diseases/surgery , Radiosurgery/instrumentation , Adult , Audiometry, Pure-Tone , Auditory Threshold/physiology , Biopsy , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/physiopathology , Decompression, Surgical/instrumentation , Facial Nerve/pathology , Facial Nerve/physiopathology , Facial Nerve/surgery , Facial Nerve Diseases/pathology , Facial Nerve Diseases/physiopathology , Female , Follow-Up Studies , Humans , Image Enhancement , Magnetic Resonance Imaging , Male , Microsurgery/instrumentation , Middle Aged , Neoplasm Grading , Postoperative Complications/etiology , Postoperative Complications/pathology , Postoperative Complications/physiopathology , Retrospective Studies , Speech Discrimination Tests , Tomography, X-Ray Computed
18.
J Clin Neurosci ; 19(6): 862-5, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22386480

ABSTRACT

Extracranial trigeminal schwannomas extending into the infratemporal fossa are rare. The traditional surgical approaches to the infratemporal fossa are associated with complications, such as facial nerve dysfunction, hearing loss, dental malocclusion and cosmetic problems. We report eight patients (four males, four females, age range=31-62 years) who were treated between 2004 and 2009 for extracranial trigeminal schwannomas extending into the infratemporal fossa. Schwannomas were surgically removed using a purely endoscopic endonasal approach. The maximum diameters of the tumours ranged from 30 mm to 70 mm and all tumours were completely removed. There were no intraoperative or postoperative complications in this series. There were no recurrences during the follow-up period which ranged from 10 to 74 months (mean=30 months). The purely endoscopic endonasal approach may provide a minimally invasive and safe approach to remove extracranial trigeminal schwannomas extending into the infratemporal fossa. Radical resection was associated with an excellent long-term outcome in this series.


Subject(s)
Cranial Nerve Neoplasms/surgery , Endoscopy/methods , Frontal Bone/pathology , Neurilemmoma/surgery , Nose/surgery , Temporal Bone/pathology , Adult , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/physiopathology , Female , Follow-Up Studies , Frontal Bone/surgery , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neurilemmoma/pathology , Neurilemmoma/physiopathology , Retrospective Studies , Temporal Bone/surgery
19.
Laryngoscope ; 122(4): 790-2, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22302608

ABSTRACT

Vagal nerve schwannomas are rare, benign, neural sheath tumors. The treatment of enlarging or symptomatic vagal nerve schwannomas is surgical resection. Transecting the vagus nerve results in significant morbidity, and attempts at nerve preservation should be made whenever possible. We introduce a nerve-sparing technique using meticulous microsurgical dissection and intraoperative nerve monitoring for vagal schwannomas. A 61-year old patient presented with an enlarging 2-cm right vagal nerve schwannoma. She underwent resection via a transcervical approach. The patient was intubated with an electromyographic (EMG) endotracheal tube that allowed for monitoring of the recurrent laryngeal nerve intraoperatively. A microsurgical subcapsular dissection was performed after branches of the vagus nerve were identified using a nerve probe and preserved. At the conclusion of the resection the nerve was intact and stimulated along its entire course. Postoperatively, the patient had normal vagal nerve function. We introduced the role of intraoperative nerve monitoring using an EMG endotracheal tube for successful enucleation of vagal schwannomas. In conjunction with meticulous microsurgical dissection, nerve monitoring allows for successful preservation of the vagus nerve and decreased postoperative morbidity.


Subject(s)
Cranial Nerve Neoplasms/surgery , Microsurgery/methods , Monitoring, Intraoperative/methods , Neurilemmoma/surgery , Recurrent Laryngeal Nerve/physiopathology , Vagus Nerve Diseases/surgery , Vagus Nerve , Cranial Nerve Neoplasms/diagnosis , Cranial Nerve Neoplasms/physiopathology , Electromyography/methods , Female , Follow-Up Studies , Humans , Magnetic Resonance Imaging , Middle Aged , Neurilemmoma/diagnosis , Neurilemmoma/physiopathology , Vagus Nerve Diseases/diagnosis , Vagus Nerve Diseases/physiopathology
20.
J Laryngol Otol ; 126(2): 120-4, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22152700

ABSTRACT

OBJECTIVES: To determine the implications of a functional approach to vestibular schwannoma surgery, with facial nerve function prioritised higher than total tumour excision. STUDY DESIGN: A case-control study in a tertiary referral neurotology clinic. PATIENTS: A 'functional' surgical group treated after April 2007 (n = 44, mean cerebellopontine angle dimension 27 mm), and an 'excisional' surgical group matched for tumour size, treated from 1997 to April 2007 (n = 115). INTERVENTION: Change to more functional surgical approach. PRIMARY OUTCOME: facial nerve status. Secondary outcome: tumour recurrence in less-than-total tumour excision. RESULTS: Facial nerve preservation: 77 per cent House-Brackmann grade I-II in functional group at 12 months, versus 57 per cent grade I-II in excisional group (p = 0.027). Tumour recurrence: 1 per cent in total excision group, 2 per cent in near-total group and 40 per cent in sub-total group. CONCLUSION: A functional approach to vestibular schwannoma surgery improves facial nerve preservation outcomes and reduces the requirement for facial nerve rehabilitative interventions. Tumour recurrence rates are low in near-totally excised lesions but significant if only sub-total excision is achieved.


Subject(s)
Cranial Nerve Neoplasms/physiopathology , Facial Nerve/physiopathology , Neoplasm Recurrence, Local/epidemiology , Neuroma, Acoustic/physiopathology , Otologic Surgical Procedures/methods , Outcome Assessment, Health Care/statistics & numerical data , Case-Control Studies , Cranial Nerve Neoplasms/surgery , Facial Paralysis/etiology , Facial Paralysis/prevention & control , Female , Humans , Male , Middle Aged , Neoplasm Recurrence, Local/diagnosis , Neuroma, Acoustic/surgery , Otologic Surgical Procedures/rehabilitation , Patient Satisfaction , Postoperative Period
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