Otology, Neurotology, and Skull Base SURGERY Clinical Reference Guide

Theodore R. McRackan, MD Derald E. Brackmann, MD

Contents Foreword by Harold C. Pillsbury, MD xi Introduction xiii Acknowledgments xv About the Editors xvi Contributors xvii Section I

History of Neurotology

1

Chapter 1

History of Neurotology and Skull Base Surgery Lawrence R. Lustig

3

Section II

Embryology Anatomy Physiology

13

Chapter 2

Embryological Development of the Ear Theodore R. McRackan and George B. Wanna

15

Chapter 3

Anatomy and Physiology of the Auditory System Gregory J. Basura and Steven A. Telian

23

Chapter 4

Anatomy and Physiology of the Vestibular System Gregory T. Whitman and Timothy C. Hain

33

Section III

Evaluation

45

Chapter 5

The Neurotologic Examination Stanley Pelosi

47

Chapter 6

Hearing Assessment René H. Gifford

55

Chapter 7

Vestibular Testing Yuri Agrawal

67

Chapter 8

Intraoperative Monitoring Christopher K. Giardina and Oliver F. Adunka

75

Section IV

Common Otologic Symptoms

83

Chapter 9

Tinnitus Theodore R. McRackan and John C. Goddard

85

v

vi   Otology, Neurotology, and Skull Base Surgery:  Clinical Reference Guide

Chapter 10

Otalgia and Temporomandibular Joint Disorders Jason A. Beyea and Aaron C. Moberly

93

Section V

Hearing Loss

99

Chapter 11

Congenital and Genetic Hearing Loss Seiji B. Shibata and Richard J. Smith

101

Chapter 12

Otosclerosis Felipe Santos and Michael J. McKenna

111

Chapter 13

Presbycusis Simon I. Angeli

119

Chapter 14

Noise-Induced Hearing Loss Brian S. Chen and William M. Luxford

125

Chapter 15

Traumatic Injuries to the Ear Bradley W. Kesser

131

Chapter 16

Autoimmune Inner Ear Disease M. Jennifer Derebery

141

Chapter 17

Sudden Sensorineural Hearing Loss David S. Haynes and Jacob B. Hunter

149

Chapter 18

Ototoxicity Joseph T. Breen and Jeffrey T. Vrabec

157

Chapter 19

Rare Causes of Hearing Loss Oliver F. Adunka and Craig A. Buchman

169

Section VI

Otologic Infections

177

Chapter 20

Otitis Externa Theodore R. McRackan and Marc L. Bennett

179

Chapter 21

Otitis Media Sujana S. Chandrasekhar

187

Chapter 22

Cholesteatoma Brendan P. O’Connell and Ted A. Meyer

197

Chapter 23

Petrous Apicitis and Intracranial Infection Anthony Myint, Joel Lavinsky, John L. Go, and Rick A. Friedman

209

CONTENTS  vii

Section VII

Hearing Rehabilitation

221

Chapter 24

Hearing Aids Monica M. Andriacchi and John W. House

223

Chapter 25

Implantable Hearing Devices Sohit Kanotra and Moises A. Arriaga

233

Chapter 26

Cochlear Implants Robert F. Labadie

247

Chapter 27

Auditory Brainstem Implants Daniel S. Roberts and Eric P. Wilkinson

259

Section VIII Skull Base Disorders

267

Chapter 28

Skull Base and Intracranial Anatomy C. Eduardo Corrales and Robert K. Jackler

269

Chapter 29

Vestibular Schwannoma Theodore R. McRackan and Derald E. Brackmann

281

Chapter 30

Meningiomas Colin L. W. Driscoll

291

Chapter 31

Neurofibromatosis Type II Brian S. Chen and William H. Slattery III

301

Chapter 32

Stereotactic Radiosurgery in Neurotology P. Ashley Wackym, Andrew Y. Kee, and Norman Jed Schroeder

309

Chapter 33

Temporal Bone Malignancy Paul W. Gidley

321

Chapter 34

Jugular Foramen Lesions Theodore R. McRackan and James L. Netterville

331

Chapter 35

Lesions of the Cerebellopontine Angle and Petrous Apex David R. Friedmann, J. Thomas Roland, Jr., and Sean O. McMenomey

341

Chapter 36

Cerebrospinal Fluid Leaks and Encephaloceles Jeffrey D. Sharon and Howard W. Francis

351

viii   Otology, Neurotology, and Skull Base Surgery:  Clinical Reference Guide

Chapter 37

Complications from Neurotologic Surgery Marc S. Schwartz

361

Section IX

Vestibular Disorders

371

Chapter 38

Bedside Vestibular Evaluation Evan Graboyes and Joel Goebel

373

Chapter 39

Ménière’s Disease Cameron C. Wick, Maroun T. Semaan, and Cliff A. Megerian

389

Chapter 40

Benign Paroxysmal Positional Vertigo Judith A. White

401

Chapter 41

Superior Semicircular Canal Dehiscence Syndrome 409 Heather M. Weinreich and John P. Carey

Chapter 42

Labyrinthitis and Vestibular Neuronitis Edward I. Cho

419

Chapter 43

Vestibular Migraine Michael Thomas Teixido

427

Chapter 44

Nonotologic Causes of Dizziness Timothy C. Hain and Marcello Cherchi

439

Chapter 45

Vestibular Therapy Elizabeth Grace Georgelos

449

Section X

Facial Nerve

459

Chapter 46

Embryology and Anatomy of the Facial Nerve Matthew L. Carlson and Alex D. Sweeney

461

Chapter 47

Electrodiagnostic Testing of the Facial Nerve Joseph P. Roche and Marlan R. Hansen

473

Chapter 48

Acute Facial Nerve Palsy Joseph P. Roche and Bruce J. Gantz

481

Chapter 49

Primary Facial Nerve Tumors Alejandro Rivas and Theodore R. McRackan

493

Chapter 50

Facial Nerve Rehabilitation Caroline A. Banks and Tessa A. Hadlock

501

CONTENTS   ix

Section XI

Pediatric Otology

511

Chapter 51

Hearing Loss Syndromes Lourdes Quintanilla-Dieck and Steven Goudy

513

Chapter 52

Congenital Aural Atresia Paul R. Lambert

525

Section XII Other Otologic Considerations

531

Chapter 53

Otologic Manifestations of Systemic Disorders J. Eric Lupo

533

Chapter 54

External Auditory Canal Lesions Elliott D. Kozin and Daniel J. Lee

545

Chapter 55

On the Horizon Justin S. Golub and Ravi N. Samy

553

Index

563

Foreword This remarkable text, edited by Drs. McRackan and Brackmann, is a significant addition to our armamentarium of references in the field of otology, neurotology, and skull base surgery. The chapters are well-written and encompass the scope of the subspecialty. Each author is a well-recognized expert in their field and the format of the chapters by outline is extremely easy to follow. It is an outstanding reference for residents, fellows, and practicing otolaryngologists as well as neurotologists. The text is simplistic and easily addresses any question that may arise in the mind of the reader. This is clearly a reference guide. No attempts have been made to increase the prose to describe the topics, but that is not to say that the key issues are hard to assess using the format. The editors are to be commended in formulating a text that is extremely user-friendly to the reader. In these days where the majority of information we seek is available on the Internet, this particular book will be a completely different offering that will be a welcome addition to anyone’s library. I look forward to receiving my copy!!! — Harold C. Pillsbury, MD Professor and Chief Otolaryngology-Head and Neck Surgery The University of North Carolina at Chapel Hill

xi

Chapter

29 Vestibular Schwannoma Theodore R. McRackan and Derald E. Brackmann

Nomenclature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 282 Epidemiology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 282 Pathophysiology . . . . . . . . . . . . . . . . . . . . . . . . . . . . 282 Presentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 283 Diagnosis and Evaluation . . . . . . . . . . . . . . . . . . . . . . 284 Natural History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 285 Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 285 Observation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 286 Microsurgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 286 Radiosurgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 289 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 289

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282   Otology, Neurotology, and Skull Base Surgery:  Clinical Reference Guide

Nomenclature • Virchow named lesion neuroma due to parallel fibers on histology appear to be axons • Initially thought to be cochlear origin due to associated hearing loss • Murrey and Stout discovered origin cell to be Schwann cell • Preferred name is currently vestibular schwannoma (VS) although acoustic neuroma is still widely used

Epidemiology • Represent approximately 6% of all intracranial tumors • Prospective Denmark database estimate approximately 20 VS per 1 million population • Incidence increasing due to awareness and improved imaging access and quality 1. 7.8 VS/million 1976 to peak 23 VS/million year 2004 • Tumor size at time of diagnosis has decreased from 30 mm in mid1970s to current 10 mm • Mean age at diagnosis has also decreased from 58 years to 49 years

Pathophysiology • Arise from vestibular division of eighth cranial nerve 1. More commonly the inferior vestibular nerve • VS do not likely arise from Obersteiner-Redlich transition zone (glialschwannian junction) as initially thought 1. Most tumors form lateral to the Obersteiner-Redlich transition zone; oligodendrocytes produce myelin medial to junction and Schwann cells lateral 2. Greatest density of Schwann cells lies at Scarpa’s ganglion; VS likely arise from Schwann cell population associated with the Scarpa’s (vestibular) ganglion; like VS, Scarpa’s ganglion can lie near junction but also at various locations • Understanding of genetic origins of sporadic VS is still uncertain; tumor biology is mostly understood through studying Neurofibromatosis type II (see Chapter 31) • There are two histological patterns; Antoni A are densely packed cells with an organized whirled appearance (Verocay body); Antoni B are more loosely packed collection of vacuolated pleomorphic cells; Antoni B may occur more frequently in large tumors 1. Stain positive for S-100

CHAPTER 29

Vestibular Schwannoma   283

Presentation • Hearing loss is most common presenting symptom and present in 95% of patients 1. Typically gradual onset unilateral sensorineural hearing loss 2. During clinical course up to 26% of patients report sudden onset SNHL 3. Normal hearing patients are more likely to have tumors 50%

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