Добавил:
Sekretar
kiopkiopkiop18@yandex.ru
t.me/Prokururor I Вовсе не секретарь, но почту проверяю
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_4507_Библиотеки_им_академика_М_И_Перельмана.pdf
X
- •Preface
- •Contents
- •1.3.4 The Eustachian Tube
- •1.3.5 Muscles
- •1.3.6 Innervation
- •1.3.7 Vascular Supply
- •1.4 The Inner Ear (Labyrinthine Cavity)
- •1.4.1 The Vestibule
- •1.4.2 Semicircular Canals
- •1.4.4 The Cochlea
- •1.4.5 Innervation
- •1.1 Introduction
- •1.2 The External Ear
- •1.2.1 The Auricle
- •1.2.3 The Eternal Auditory Canal/External Acoustic Meatus
- •1.3 The Middle Ear (Tympanic Cavity)
- •1.3.1 The Tympanic Membrane
- •1.3.3 Ossicles
- •1.4.6 Cochlea Nerve Anatomy
- •1.4.7 Vestibular Nerves
- •1.4.8 The Vestibulocochlear Nerve
- •1.5 The Central Hearing System
- •1.5.3 Auditory Input
- •1.5.4 The Auditory Nerve’s Descending Routes
- •References
- •2: Outer–Middle–Inner Ear Embryology
- •2.1 Introduction
- •2.2 Embryology
- •2.3.1 First Week
- •2.3.3 Third Week
- •2.3.4 Fourth Week
- •2.3.5 Sixth Week
- •References
- •3.1 Introduction
- •3.3 The Outer Ear
- •3.3.1 Anatomy
- •3.3.3 Localization
- •3.4 The Middle Ear
- •3.4.3 Middle Ear Muscles
- •3.4.4 The Eustachian Tube
- •3.4.5 Impedance Matching
- •3.5 The Inner Ear
- •3.5.1.1 Lateral Wall
- •3.5.1.2 Reissner’s Membrane
- •3.5.1.3 The Basilar Membrane
- •3.5.2.1 Hair Cells
- •Inner Hair Cells
- •Outer Hair Cells
- •3.5.3 The Tectorial Membrane
- •3.5.4 The Osseous Spiral Lamina
- •3.5.5 Cochlear Mechanics
- •3.5.5.1 Passive Mechanics
- •3.5.5.2 Active Mechanics
- •3.6.1 Auditory Nerve Fibers
- •3.6.2 The Subcortical Auditory Nuclei
- •3.6.2.1 The Cochlear Nucleus
- •3.6.2.2 The Superior Olivary Complex
- •3.6.2.3 The Lateral Lemniscus
- •3.6.2.4 Inferior Colliculus
- •3.6.2.5 The Medial Geniculate Body
- •3.6.3 The Auditory Cortex
- •3.7 Conclusion
- •References
- •4.1 Introduction
- •4.2 Eustachian Tube Anatomy
- •4.4 Eustachian Tube Dysfunction
- •References
- •5: Temporal Bone Radiology
- •5.1.1 Introduction
- •5.1.2 Computed Tomography (CT)
- •5.1.3 Temporal Bone CT Angiography
- •5.1.4 Magnetic Resonance Imaging (MRI)
- •5.1.5 Diffusion-Weighted Imaging (DWI)
- •5.1.6 Conclusion
- •5.2.1 Introduction
- •5.2.2.1 The External Auditory Canal (EAC)
- •5.2.3 Temporal Bone Fractures
- •5.2.4 Conclusion
- •5.3.1 Introduction
- •5.3.2 Necrotizing Otitis Externa
- •5.3.3 Middle Ear
- •5.3.3.2 Chronic Otitis Media
- •5.3.3.3 Cholesteatomas
- •5.3.3.4 Cholesterol Granulomas
- •5.3.4 Inner Ear
- •5.3.4.1 Labyrinthitis
- •5.3.4.2 Petrous Apicitis
- •5.3.5 Conclusion
- •5.4.1 Introduction
- •5.4.2.1 Cerebellopontine Angle Tumors
- •Vestibular Schwannomas
- •Arachnoid Cysts
- •Meningiomas
- •5.5.2 External Auditory Canal Aplasia
- •5.5.4 Inner Ear Malformations
- •5.5.4.1 Complete Labyrinthine Aplasia/Michel Anomaly
- •5.5.4.2 Rudimentary Otocysts
- •5.5.4.3 Common Cavity Malformation
- •5.5.4.4 Incomplete Partition (IP) Type I
- •5.5.4.5 Incomplete Partition Type II/Mondini Malformation
- •5.5.4.6 Incomplete Partition Type III
- •5.5.4.7 Cochlear Anomalies
- •5.5.4.8 Semicircular Canal Anomalies
- •5.5.6 Conclusion
- •5.6.1 Introduction
- •5.6.2 Otospongiosis/Otosclerosis
- •Epidermoids
- •5.4.2.2 The Middle Ear
- •5.4.2.4 Petrous Bone
- •5.4.2.5 Metastatic Tumors
- •5.4.3 Conclusion
- •5.5.1 Introduction
- •5.6.3 Third Window Lesions
- •5.6.4 Conclusion
- •References
- •6.1 Introduction
- •6.3.1 What Is Sound?
- •6.3.2 Sound Intensity
- •6.4 Psychoacoustics
- •6.4.1 Signal Detection Theory
- •References
- •7.1 Introduction
- •7.1.1 What Is Sound?
- •7.2 Fundamental Acoustic Concepts
- •7.2.3 Period
- •7.2.4 Frequency
- •7.2.5 Wavelength
- •7.3 Psychoacoustics
- •7.3.1 Loudness
- •7.3.2 Auditory Masking
- •7.3.2.1 Simultaneous Masking
- •7.3.2.2 Temporal Masking
- •7.4.2 Spatial Hearing
- •References
- •8.1 Introduction
- •8.2 Case History
- •8.3 The Audiology Test Room
- •8.4.1 Pure-Tone Audiometry
- •8.4.1.1 Masking
- •8.4.2 Speech Audiometry
- •8.4.3 Pediatric Assessment
- •8.5.1 Acoustic Immittance Audiometry
- •8.5.1.1 Tympanometry
- •Tympanogram Interpretation
- •8.5.1.2 Multifrequency Tympanometry
- •8.5.1.3 Wideband Tympanometry
- •8.5.1.4 Acoustic Reflex Test
- •8.5.1.5 The Reflex Decay Test
- •8.5.1.6 Eustachian Tube Evaluation
- •8.5.2 Otoacoustic Emissions
- •8.5.2.2 Performing Otoacoustic Emission Tests
- •8.5.3 Auditory Evoked Potentials
- •8.5.3.2 Auditory Evoked Brainstem Response
- •Stimulus Types
- •Stimulus Polarity
- •Stimulus Presentation Rate
- •Stimulus Intensity
- •Analysis Time (Recording Epoch)
- •Filters
- •Artifact Rejection Level
- •Electrodes
- •8.5.3.3 Auditory Steady-State Responses
- •8.5.3.4 Electrocochleography
- •Electrocochleography Analysis
- •8.5.3.5 Cortical Auditory Evoked Potentials
- •8.5.3.6 Event-Related Auditory Potentials
- •P300
- •Mismatch Negativity
- •Acoustic Change Complex
- •8.6 Conclusion
- •References
- •9.1 Introduction
- •9.2.3 Conductive Hearing Loss
- •9.2.4 Sensorineural Hearing Loss
- •9.2.4.1 Internal Acoustic Canal Tumors
- •9.2.4.2 Auditory Neuropathy Spectrum Disorder
- •9.2.4.3 Third Window Syndrome
- •9.2.4.4 Dead Region
- •9.2.5 Mixed Hearing Loss
- •9.3 Hearing Loss Configuration
- •9.3.3 Unilateral or Bilateral Hearing Loss
- •9.3.4 Symmetric or Asymmetric Hearing Loss
- •9.3.5 Fluctuating or Stable Hearing Loss
- •9.4 Diagnostic Tests
- •9.4.1 Pure Tone Threshold Testing
- •9.4.2 Speech Recognition Tests
- •9.4.3 Tympanometric Tests
- •9.4.4 Stapedial Reflex
- •9.4.5 Otoacoustic Emission Test
- •9.4.6 Auditory Brainstem Responses
- •9.6 Reporting Audiological Findings
- •9.7 Conclusion
- •References
- •10.1 Introduction
- •10.2.1 Anamnesis
- •10.2.2 Hearing Loss
- •10.2.3 Ear Pain (Otalgia)
- •10.2.4 Ear Discharge (Otorrhea)
- •10.2.5 Itchy Ear
- •10.2.8 Physical Examination
- •10.2.8.1 Inspection
- •10.2.8.2 Palpation
- •10.2.8.3 Otoscopy
- •10.2.12 Hearing Examination
- •10.2.13 Hearing Assessment
- •10.2.13.1 Whisper Test
- •10.2.13.2 Tuning Fork Tests
- •Rinne Test
- •Weber Test
- •Schwabach Test
- •Gelle Test
- •10.3 Conclusion
- •References
- •11.1 Introduction
- •11.2.1 Microphone
- •11.2.2 Amplifier
- •11.2.3 Receiver
- •11.2.4 Batteries
- •11.2.5 Earmolds/Domes
- •11.4 Hearing Aid Types
- •11.5.1 Directional Microphone Technologies
- •11.5.2 Digital Noise Reduction
- •11.5.3 Frequency Lowering
- •11.5.4 Feedback Canceller
- •11.5.5 Bluetooth
- •11.6 Other Hearing Aid Technologies
- •11.7 Pediatric Hearing Aid Application
- •11.7.3.7 Hearing Aid Fitting
- •Prescription Formula Preference
- •Objective Verification Tools
- •Subjective Verification Tools
- •Fine-Tuning
- •11.8 Adult Hearing Aid Application
- •11.8.1.1 Medical Evaluation
- •11.8.1.2 Audiological Evaluation
- •11.8.1.3 Physical Evaluation
- •11.8.1.4 Psychological Evaluation
- •11.8.2 Hearing Aid Application Process
- •11.8.2.1 Anamnesis
- •11.8.2.6 Hearing Aid Fitting
- •Fine-Tuning
- •11.9 Conclusion
- •11.10 Case Studies
- •11.10.1 Case 1
- •11.10.2 Case 2
- •11.10.3 Case 3
- •11.10.4 Case 4
- •References
- •12.1 Introduction
- •12.3.1 Pathophysiology
- •12.3.2 Management
- •12.3.3 Etiology
- •12.3.4 Epidemiology
- •12.3.5 Assessing
- •12.3.6 Treatment
- •References
- •13: Otoplasty
- •13.1 Introduction
- •13.2 General Information
- •13.2.1 Auricular Anthropometry
- •13.3 History
- •13.8.1 Conservative Treatment
- •13.8.2 Surgical Treatment
- •13.11 Patient Follow-Up
- •13.12 Case Examples
- •13.13 Complications
- •13.13.1 Early Complications
- •13.13.2 Late Complications
- •13.13.3.1 Telephone Ear Deformity
- •13.13.3.2 Reverse Telephone Ear Deformity
- •13.13.3.5 Antihelical Malposition
- •13.13.3.6 Tragal Prominence
- •13.13.3.7 Auricular Lines
- •13.14 Revision Otoplasty
- •References
- •14: External Ear Tract Diseases
- •14.1 Introduction
- •14.2.1 Atopic Dermatitis
- •14.2.2 Allergic Contact Dermatitis
- •14.2.3 Photoallergic Dermatitis
- •14.2.4 Psoriasis
- •14.2.5 Relapsing Polychondritis
- •14.2.6 Gout
- •14.3 Traumatic Disorders
- •14.3.1 Irritant Contact Dermatitis
- •14.3.2 Phototoxic Dermatitis
- •14.3.3 Phototrauma
- •14.4 Infectious Diseases
- •14.4.1 Otitis Externa
- •14.4.1.1 Background
- •14.4.1.2 Anatomy
- •14.4.1.3 Classification
- •14.4.1.5 Diagnosis
- •14.4.1.6 Management
- •References
- •15: Auricula Tumors
- •15.1 Introduction
- •15.2 Benign Tumors
- •15.2.1 Chondrodermatitis Nodularis Chronica Helicis
- •15.2.2 Cystic Chondromalacia
- •15.2.3 Ceruminous Gland Adenoma
- •15.3 Malign Tumors
- •15.3.1 Basal Cell Carcinoma (BCC)
- •15.3.2 Squamous Cell Carcinoma
- •15.3.3 Ceruminous Gland Adenocarcinoma
- •15.4 Conclusion
- •References
- •16: Acute Suppurative Otitis Media
- •16.1 Introduction
- •16.2 Pathophysiology
- •16.3 Etiology
- •16.3.1 Host Factors
- •16.3.1.1 Immune System
- •16.3.1.2 Hereditary Susceptibility
- •16.3.1.3 Mucins
- •16.3.1.4 Anatomic Abnormalities
- •16.3.1.5 Physiologic Dysfunction
- •16.3.2 Infectious Factors
- •16.3.2.1 Bacterial Pathogens
- •16.3.2.2 Viral Pathogens
- •16.3.3 Environmental Factors
- •16.3.3.1 Infant Feeding Methods
- •16.4 Classification
- •16.6 Diagnosis
- •16.7 Treatment
- •16.7.1 Antibiotic Therapy Versus Observation
- •16.7.2 Initial Antibiotic Therapy
- •16.7.3 Supplemental Programs
- •References
- •17.1 Introduction
- •17.2 Definition
- •17.4 Pathophysiology
- •17.5 Diagnosis
- •17.5.1 Clinical Evaluation
- •17.6 Treatment
- •17.6.1 Medical Treatment
- •17.6.2 Surgical Treatment
- •17.7 Conclusion
- •References
- •18: Chronic Suppurative Otitis Media
- •18.1 Introduction
- •18.2 Epidemiology
- •18.3 Pathophysiology
- •18.4 Microbiology
- •18.5 Histopathology
- •18.6 Clinical Manifestations
- •18.6.1 Tubotympanic Type
- •18.6.2 Atticoantral Type
- •18.7 Diagnosis
- •18.7.1 Anamnesis
- •18.7.2 Otoscopic Examination
- •18.7.3 Audiological Evaluation
- •18.7.4 Imaging
- •18.8 Treatment
- •18.8.1 Medical Treatment
- •18.8.2 Surgical Treatment
- •18.9 Complications
- •18.10 Future Directions
- •18.11 Conclusion
- •References
- •19: Cholesteatoma
- •19.1 Introduction
- •19.2 Definition
- •19.3 Epidemiology
- •19.4 Histopathology
- •19.7 Cholesteatoma Types
- •19.7.1 Congenital Cholesteatoma
- •19.7.2 Acquired Cholesteatoma
- •19.7.2.2 Epithelial Migration Theory
- •19.7.2.3 Basal Cell Hyperplasia Theory
- •Tos Staging
- •Sade Staging
- •19.7.3 Unclassified Cholesteatomas
- •19.7.4 Petrous Bone Cholesteatomas
- •19.8 Practical Classification
- •19.8.1 Attic Cholesteatomas
- •19.8.2 Sinus Cholesteatomas
- •19.8.3 Pars Tensa Cholesteatomas
- •19.9 Clinical Presentations
- •19.9.1 Cholesteatoma Microbiology
- •19.10 Diagnosis
- •19.10.2 Computed Tomography
- •19.10.3 Magnetic Resonance Imaging
- •19.10.4 Audiometric Evaluation
- •19.11.1 Closed Techniques
- •19.11.2 Open Techniques
- •19.12 Conclusion
- •References
- •20.1 Introduction
- •20.2 Physiology
- •20.2.4 Tympanic Isthmus
- •20.4 Pathophysiology
- •20.5 Clinical Picture
- •20.6 Management
- •20.6.1 Surgical Management
- •20.6.1.2 Tympanoplasty
- •20.6.1.3 Mastoid Surgery
- •20.7 Adhesive Otitis Media
- •20.7.1 Pathogenesis
- •20.7.2 Clinical Findings
- •20.7.3 Imaging
- •20.7.4 Treatment
- •20.8 Conclusion
- •References
- •21.1 Introduction
- •21.2 Intratemporal Complications
- •21.2.1 Acute Mastoiditis
- •21.2.2 Facial Nerve Paralysis
- •21.2.3 Labyrinthitis
- •21.2.4 Labyrinthine Fistula
- •21.2.5 Petrositis
- •21.3 Intracranial Complications
- •21.3.1 Meningitis
- •21.3.2 Lateral Sinus Thrombosis
- •21.3.3 Brain Abscess
- •21.3.4 Otitic Hydrocephalus
- •21.3.5 Epidural Abscess
- •21.3.6 Subdural Empyema
- •21.4 Conclusion
- •References
- •22: Basic Otological Surgical Techniques
- •22.1 Introduction
- •22.3 Atticotomy
- •22.4 Mastoidectomy
- •22.4.1 Simple (Cortical) Mastoidectomy
- •22.4.2 Canal Wall-Up Mastoidectomy
- •22.4.3 Canal Wall-Down Mastoidectomy
- •22.4.4 Retrograde Mastoidectomy
- •22.4.5 Modified Radical Mastoidectomy
- •22.4.6 Radical Mastoidectomy
- •22.4.7 Mastoid Obliteration
- •22.5 Petrosectomy
- •22.6 Conclusion
- •References
- •23: Tympanoplasty
- •23.1 Introduction
- •23.2.1 Chronic Otitis Media
- •23.2.2 Traumatic Perforations
- •23.5 Tympanoplasty Types
- •23.7 Graft Materials
- •23.8 Graft Techniques
- •23.8.1 The Perichondrium/Cartilage Island Graft
- •23.8.2 The Palisade Graft
- •23.8.3 The Temporalis Fascia Graft
- •23.9 Surgical Approaches
- •23.9.1 Microscopic Approach
- •23.9.2 Endoscopic Approach
- •23.10.1 Transmeatal Incisions
- •23.10.1.1 The Rosen Incision
- •23.10.1.3 Anterior Tympanomeatal Flap
- •23.10.2 Endaural Incision
- •23.10.3 Postauricular Incision
- •23.11 Pediatric Tympanoplasty
- •23.12 Prognostic Factors
- •23.14 Conclusion
- •References
- •24: Ossiculoplasty
- •24.1 Introduction
- •24.4 Indications/Contraindications
- •24.5 Reconstruction Materials
- •24.7 Surgical Preparation
- •24.8 Surgical Technique
- •24.9 Ossiculoplasty Results
- •24.10 Complications
- •24.11 Postoperative Care
- •24.12 Follow-Up
- •24.13 Conclusion
- •References
- •25: Tympanomastoidectomy
- •25.1 Introduction
- •25.2 Surgical Anatomy
- •25.4 Indications
- •25.5 Technique
- •25.5.1 Patient’s Preparation
- •25.5.3 Simple Mastoidectomy
- •25.5.4 Posterior Tympanostomy or Facial Recess Approach
- •25.5.5 Epitympanectomy
- •25.5.6 Endolymphatic Sac Procedures
- •25.5.8 Atticotomy-Atticoantrotomy

398
M. Tan et al.
19.10.4 Audiometric Evaluation
Every patient with chronic otitis media should be evaluated audiologically. If the
cholesteatoma involves the ossicular chain, conductive hearing loss will result. If
the cochlea is also involved, sensorineural hearing loss is added to the picture. If
both situations are present, it is called mixed hearing loss. Normal hearing does not
exclude cholesteatoma. Although a cholesteatoma damages the ossicular chain by
causing mass effect conduction, it may cause hearing to be better than it should be.
Tympanometry ndings are not specic to cholesteatoma [97–99].
19.11 Treatment ofCholesteatomas
Cholesteatoma is treated surgically. The purpose of surgery is to completely remove
the disease, leaving no residual disease and no opportunity for recurrent cholesteatoma development. The lesions found after surgical treatment of cholesteatoma can
be classied as residual cholesteatoma and recurrent cholesteatoma. Residual cholesteatoma is the leaving of cholesteatoma matrix in the middle ear, mastoid cavity,
and especially in graft intact and vital patients without retraction pouch in the postoperative period. On the other hand, recurrent cholesteatoma refers to the picture in
which cholesteatoma recurs in patients who have undergone surgery for eradication
of cholesteatoma and causes discomfort in the postoperative period, and retraction
pouch, graft perforation or attic destruction is seen in otoscopic examination.
Complete clearance of the disease should be the priority, and if functional procedures are necessary, they can be postponed to later sessions. Open and closed techniques are used in surgery. The closed technique preserves or reconstructs the
posterior wall of the external auditory canal in an attempt to create a ventilated
physiologic middle ear. The open technique removes the posterior wall of the external auditory canal and combines the middle ear cavity and the mastoidectomy cavity into a single cavity.
19.11.1 Closed Techniques
In this technique, the posterior wall of the external auditory canal is preserved or
repaired after removal and the posterior wall is rebuilt. This repair may be accomplished by replacing the removed posterior bone wall with otologic materials such
as cartilage, cortical bone, or alloplastic materials such as titanium.
In the classic closed technique, a complete mastoidectomy is performed through
a retroauricular incision. After ensuring that the aditus ad antrum is open, the tympanomeatal ap is lifted and the middle ear is entered. After cleaning the cholesteatoma in the mastoid and middle ear, ossicular chain reconstruction and tympanic
membrane repair can be performed. Preservation of the posterior wall of the external auditory canal, ventilated mastoid cavity, and provision of physiologic middle
ear ventilation are among the advantages of this technique. Due to inadequate access

19 Cholesteatoma
399
to the facial recess and extension of the tympanic sinus of posterior mesotympanic
cholesteatomas developed from retraction pockets, especially in the pars tensa of
the posterior upper segment, the use of this technique in such situations will increase
the recurrence rate. Residual cholesteatoma results from inadequate cleaning of the
epithelium during closed procedures. Residual cholesteatoma can be seen in the
postoperative period as well as after planned second-look procedures. Planned second-look surgery is recommended one year after surgery in children and two years
after surgery in adults. Residual cholesteatomas have a well-capsulated, pearl-like
appearance and do not contact the tympanic membrane unless they are too large.
Although MRI is helpful in the presence of residual cholesteatoma, it may not be
diagnostic. The sites where residual disease is most commonly seen after closed
surgery are those segments that are difcult to clean, such as the posterior mesotympanum (around the tympanic sinus and stapes), anterior epitympanum, and rarely
the mastoid and hypotympanum. The most difcult cases are those in which the
cholesteatoma moves to the posterior of the labyrinth. If the residual cholesteatoma
has a pearl-like shape, removal of the cholesteatoma is easy and effective in the
second session. If the cholesteatoma does not have a capsule border, this is a negative nding in terms of prognosis. If the cholesteatoma extends to the mastoid
antrum, a complete mastoidectomy should be performed and all cells should be
opened and cleaned. Posterior tympanotomy is a method used in closed cholesteatoma surgery. With this method, facial recess cholesteatoma can be cleaned more
easily, and in the case of anterior, posterior isthmus closure, by establishing the
connection between the mastoid and the middle ear, mastoid ventilation can be
ensured. Because this method provides access to the lateral side of the facial recess,
the medial tympanic sinus is difcult to access. With the advent of otoendoscopes,
this method is no longer used for cholesteatoma surgery. In posterior tympanotomy,
a diamond burr is used to create the fossa incudis with the distance between the
second elbow lateral facial canal and the corda tympany. This is a method that has
recently been used to place a cochlear implant.
Otoendoscopes that allow access to the sinus tympany and facial recess through
closed methods minimize the risk of residual disease. It is possible to completely
dominate the facial recess with a 30-degree endoscope and the sinus tympany with
a 70-degree endoscope. In addition, the middle ear, Eustachian tube entrance, mastoidectomy region, and aditus can be examined in detail and the presence of epithelium can be checked. A meta-analysis study showed a lower rate of residual
cholesteatoma in pediatric patients who underwent endoscopic cholesteatoma surgery compared to microscopic cholesteatoma surgery [100]. Endoscopy has both
advantages and disadvantages. The sense of depth may be lost, and the stapes head
and facial nerve may be damaged. Working with one hand, staining of the endoscope lenses by even a drop of blood, and damage to the facial nerve and inner ear
structures by the heat released by the endoscope are some disadvantages of
endoscopy.
If the cholesteatoma has invaded the medial part of the incudomalleal complex,
it is rather difcult to clean this cholesteatoma with the endoscope. It is possible
to inspect this region by removing the head of the malleus and the body of the

400
M. Tan et al.
incus. It is possible that cholesteatoma developing from posterior mesotympanic
and posterior epitympanic pockets may spread to these regions. Attention should
be paid to the horizontal segment of the facial nerve medial to these bones as they
are removed.
In cases where posterior epitympanic cholesteatomas extend through the attic
to the aditus, an atticotomy should be performed and the remaining tissue completely cleaned. The scutum should also be completely cleaned during the
atticotomy.
To prevent recurrence of cholesteatoma, reconstruction of scutum defects,
obliteration of mastoidectomy cavity and formation of resistant tympanic membranes should be performed. In cases where the scutum defect is not repaired and
the ossicular chain is absent, new retraction pockets may develop from these
regions and at epithelial progression from the weak areas may be observed.
Therefore, repair should be performed. If the negative pressure in the middle ear
persists after tympanoplasty, the transplanted graft may retract and lead to recurrent disease. Because unhealthy mucosa in the remaining mastoid in this region
after cholesteatoma removal in the mastoid may not perform gas exchange and
lead to negative pressure formation, many opinions support obliteration. However,
there are other opinions that this region traps air and acts as a reservoir for the
middle ear, and therefore it is not appropriate to obliterate it. Obliteration is most
commonly used in open techniques to reduce the cavity. Obliteration may allow
reconstruction of the middle ear in open surgery and prevent the recurrence of the
disease. If obliteration is to be performed, it is important to ensure that there is no
epithelium left in the area.
19.11.2 Open Techniques
In open technique surgery for cholesteatoma, the goal is to create a cavity from the
mastoidectomy cavity and the middle ear. As a result of the surgery, the cavity can
be left completely open and it is also possible to perform reconstruction by creating
middle ear cavity. Cholesteatoma can be completely removed during these operations. Anterior epitympanum and sinus tympanum, which are difcult to access in
the closed technique, can be easily exposed and cleaned. The recurrence rate is
lower compared to the closed technique [101]. However, the need for regular care of
the cavity and restriction of the patient from water sports in the postoperative period
are the disadvantages of the open technique. The involvement of the cholesteatoma,
the damage caused, the age of the patient, and the status of the opposite ear are
important factors in determining the type of surgery. Open rather than closed surgery should be considered for cholesteatoma involving the Eustachian tube, cholesteatoma in the tympanic sinus that cannot be controlled endoscopically, erosion of
the posterior wall of the external auditory canal, labyrinthine stula that cannot be
controlled, and cholesteatoma in the only hearing ear. Because the risk of residual
cholesteatoma is higher with the closed technique than with the open technique,
close follow-up of the patient is important. In elderly patients who cannot come for

19 Cholesteatoma
401
close follow-up and who do not have high functional expectations, the open technique is preferred to the closed technique. If the patient has Eustachian tube dysfunction and a small mastoid, such patients are at risk for recurrent disease.
Therefore, the open technique may be recommended in such cases. Patients who
have undergone open surgery should have regular cavity control. If an adequate cavity is created, debris accumulation will be minimal. Reduction of the mastoidectomy cavity by obliteration may be helpful in solving postoperative cavity problems
[102]. At the end of the surgery, the external auditory meatus is adequately dilated
by resection of large cartilaginous tissues from the cavum concha. When choosing
the technique for cholesteatoma surgery, the status of the cholesteatoma and the
patient should be considered, and it is necessary to know that these two techniques
are not different methods used against each other, but they are complementary
techniques.
One of the methods of open technique, Bondy surgery is applied in the attic
region cholesteatoma. The healthy middle ear is not touched and the cholesteatoma
in the attic region is cleaned.
In pediatric patients, the closed technique is usually preferred for cholesteatoma.
However, due to the aggressive nature of cholesteatoma in this age group, second
and third-look surgery may be necessary. Both residual and recurrent cholesteatomas may recur years after initial surgery. Therefore, long-term follow-up of patients
with cholesteatoma should be planned.
One of the major problems of cholesteatoma surgery is the possibility of postoperative residual or recurrent cholesteatoma. While recurrent cholesteatoma can be
caused by recurrent retractions, residual cholesteatoma is caused by residual epithelial debris that cannot be completely removed. The way to prevent this is to clean the
cholesteatoma so that no epithelial debris remains. The use of various chemicals
such as MESNA (sodium-2-mercaptoethanesulfonate) has been proposed to achieve
this. It has been reported that MESNA allows easy dissection of the cholesteatoma
epithelium because it breaks disulde bonds in the epithelium, thus reducing the
possibility of residual cholesteatoma by preventing epithelial debris in the surgical
eld [103–107]. It has also been reported that the use of chemicals such as 5 uorouracil may prevent the development of cholesteatoma [108]. The most important
situation limiting the use of chemical agents in middle ear surgery is the possibility
of facial paralysis and inner ear toxicity. No such side effects have been reported in
studies on MESNA [109, 110].
Several methods and radiologic imaging techniques are used to follow patients
after surgery. However, the ideal imaging technique and its timing have not been
claried. Thin-slice CT at follow-up does not show recurrent cholesteatoma, but it
is possible to see the bone erosion caused by cholesteatoma. However, it is not easy
to understand whether this erosion is caused by the primary surgery or a recurrent
cholesteatoma. Studies have shown high sensitivity and specicity of non-EPI DW
MRI in detecting residual or recurrent cholesteatoma after surgery [95, 96]. The
presence or absence of residual cholesteatoma can be assessed by endoscopy after
primary surgery. If residual cholesteatoma is suspected in the patient after followup, the mastoidectomy cavity and epitympanum can be examined by endoscopy.

402
M. Tan et al.
19.12 Conclusion
Cholesteatoma is the most common and life-threatening form of chronic otitis media.
Despite extensive research, the etiopathogenesis of cholesteatoma is not fully understood. The main characteristic of cholesteatoma is that it causes bone loss. The main
reason why cholesteatoma causes complications is that it causes lytic lesions in the
bone. Early diagnosis and treatment of the disease is very important. In addition, a
comprehensive understanding of the past and recent advances in biomolecular research
on acquired cholesteatoma may assist in the development of an effective management
strategy, given that no valid nonsurgical treatment has been developed to date.
References
1. Semaan MT, Megerian CA.The pathophysiology of cholesteatoma. Otolaryngol Clin N Am.
2006;39(6):1143–59. https://doi.org/10.1016/j.otc.2006.08.003.
2. Maresh A, Martins OF, Victor JD, Selesnick SH. Using surgical observations of ossicular
erosion patterns to characterize cholesteatoma growth. Otol Neurotol. 2011;32(8):1239–42.
https://doi.org/10.1097/MAO.0b013e31822e5b5d.
3. Ferlito A.A review of the denition, terminology and pathology of aural cholesteatoma. J
Laryngol Otol. 1993;107(6):483–8. https://doi.org/10.1017/s0022215100123539.
4. Gray JD.The chronic ear. The treatment of cholesteatoma in children. Proc R Soc Med. 1964
Sep;57(9):769–71.
5. Lazard DS, Roger G, Denoyelle F, Chauvin P, Garabédian EN.Congenital cholesteatoma:
risk factors for residual disease and retraction pockets--a report on 117 cases. Laryngoscope.
2007;117(4):634–7. https://doi.org/10.1097/mlg.0b013e318030ac8c.
6. Olszewska E, Wagner M, Bernal-Sprekelsen M, Ebmeyer J, Dazert S, Hildmann H, Sudhoff
H.Etiopathogenesis of cholesteatoma. Eur Arch Otorrinolaringol. 2004;261(1):6–24. https://
doi.org/10.1007/s00405- 003- 0623- x.
7. Kalia M, Dass A, Singhal SK, Gupta N. Comparative study of cholesteatoma in paediatric and adult patients. J Laryngol Otol. 2022;136(8):765–8. https://doi.org/10.1017/
S0022215122001104.
8. Xie S, Wang X, Ren J, Liu W.The role of bone resorption in the etiopathogenesis of acquired
middle ear cholesteatoma. Eur Arch Otorrinolaringol. 2017;274(5):2071–8. https://doi.
org/10.1007/s00405- 016- 4422- 6.
9. Lee ST. Cholesteatoma in an Asian population. Acta Otolaryngol. 1991;111(3):536–41.
https://doi.org/10.3109/00016489109138380.
10. Khalid-Raja M, Tikka T, Coulson C. Cholesteatoma: a disease of the poor (socially
deprived)? Eur Arch Otorrinolaringol. 2015;272(10):2799–805. https://doi.org/10.1007/
s00405- 014- 3285- y.
11. Harris L, Cushing SL, Hubbard B, Fisher D, Papsin BC, James AL.Impact of cleft palate type on the incidence of acquired cholesteatoma. Int J Pediatr Otorhinolaryngol.
2013;77(5):695–8. https://doi.org/10.1016/j.ijporl.2013.01.020.
12. Bonnard Å, Engmér Berglin C, Wincent J, etal. The risk of cholesteatoma in individuals with
rst-degree relatives surgically treated for the disease. JAMA Otolaryngol Head Neck Surg.
2023;149(5):390–6. https://doi.org/10.1001/jamaoto.2023.0048.
13. Louw L.Acquired cholesteatoma: summary of the cascade of molecular events. J Laryngol
Otol. 2013;127(6):542–9. https://doi.org/10.1017/S0022215113000601.
14. Kupper TS.The activated keratinocyte: a model for inducible cytokine production by nonbone marrow-derived cells in cutaneous inammatory and immune responses. J Invest
Dermatol. 1990;94(6 Suppl):146S–50S. https://doi.org/10.1111/1523- 1747.ep12876130.

19 Cholesteatoma
15. Maniu A, Harabagiu O, Perde Schrepler M, Cătană A, Fănuţă B, Mogoantă CA.Molecular
biology of cholesteatoma. Romanian J Morphol Embryol. 2014;55(1):7–13.
16. Albino AP, Reed JA, Bogdany JK, Sassoon J, Parisier SC.Increased numbers of mast cells in
human middle ear cholesteatomas: implications for treatment. Am J Otol. 1998;19(3):266–72.
17. Schilling V, Bujía J, Negri B, Schulz P, Kastenbauer E. Immunologically activated
cells in aural cholesteatoma. Am J Otolaryngol. 1991;12(5):249–53. https://doi.
org/10.1016/0196- 0709(91)90001- v.
18. Akimoto R, Pawankar R, Yagi T, Baba S.Acquired and congenital cholesteatoma: determination of tumor necrosis factor-alpha, intercellular adhesion molecule-1, interleukin-1-alpha
and lymphocyte functional antigen-1in the inammatory process. ORL J Otorhinolaryngol
Relat Spec. 2000;62(5):257–65. https://doi.org/10.1159/000027756.
19. Suchozebrska-Jesionek D, Szymański M, Kurzepa J, Gołabek W, Stryjecka-Zimmer
M.Gelatinolytic activity of matrix metalloproteinases 2 and 9in middle ear cholesteatoma. J
Otolaryngol Head Neck Surg. 2008;37(5):628–32.
20. Ars B.Physiology of Eustachian tube dysfunction. In: Sudhoff H, editor. Eustachian Tube
dysfunction. 2nd ed. Bremen: UNI-MED; 2017, ISBN 978-3-8374-1535-3.
21. Baráth K, Huber AM, Stämpi P, Varga Z, Kollias S. Neuroradiology of cholesteatomas.
AJNR Am J Neuroradiol. 2011;32(2):221–9. https://doi.org/10.3174/ajnr.A2052.
22. Tos M. Incidence, etiology and pathogenesis of cholesteatoma in children. Adv
Otorhinolaryngol. 1988;40:110–7. https://doi.org/10.1159/000415679.
23. Sanna M, Mazzoni A, Landol M, Aristegui M. Tratamiento del colesteatoma intrapetroso (CIP) [Treatment of petrous bone cholesteatoma]. Acta Otorrinolaringol Esp.
1994;45(3):143–52.
24. Yung M, Tono T, Olszewska E, Yamamoto Y, Sudhoff H, Sakagami M, Mulder J, Kojima H,
İncesulu A, Trabalzini F, Özgirgin N.EAONO/JOS joint consensus statements on the denitions, classication and staging of middle ear cholesteatoma. J Int Adv Otol. 2017;13(1):1–8.
https://doi.org/10.5152/iao.2017.3363.
25. Egilmez OK, Hanege FM, Kalcioglu MT, Kaner T, Kokten N.Tegmen tympani defect and
brain herniation secondary to mastoid surgery: case presentation. Case Rep Otolaryngol.
2014;2014:756280. https://doi.org/10.1155/2014/756280.
26. Jang HB, Lee JM, Kim DJ, Lee SH, Lee IW, Lee HM.Treatment results for congenital cholesteatoma using transcanal endoscopic ear surgery. Am J Otolaryngol. 2022;43(5):103567.
https://doi.org/10.1016/j.amjoto.2022.103567.
27. Nelson M, Roger G, Koltai PJ, Garabedian EN, Triglia JM, Roman S, Castellon RJ, Hammel
JP.Congenital cholesteatoma: classication, management, and outcome. Arch Otolaryngol
Head Neck Surg. 2002;128(7):810–4. https://doi.org/10.1001/archotol.128.7.810.
28. Michaels L.An epidermoid formation in the developing middle ear: possible source of cholesteatoma. J Otolaryngol. 1986;15(3):169–74.
29. Hong SM, Lee JH, Park CH, Kim HJ.Congenital cholesteatoma localized to the tip of the
mastoid bone: a case report and possible etiology. Korean J Audiol. 2014;18(2):85–8. https://
doi.org/10.7874/kja.2014.18.2.85.
30. Karmody CS, Byahatti SV, Blevins N, Valtonen H, Northrop C.The origin of congenital
cholesteatoma. Am J Otol. 1998;19(3):292–7.
31. Kayhan FT, Mutlu C, Schachern PA, Le CT, Paparella MM.Signicance of epidermoid formations in the middle ear in fetuses and children. Arch Otolaryngol Head Neck Surg. 1997
Dec;123(12):1293–7. https://doi.org/10.1001/archotol.1997.01900120043006.
32. Lee TS, Liang JN, Michaels L, Wright A. The epidermoid formation and its afnity to
congenital cholesteatoma. Clin Otolaryngol Allied Sci. 1998;23(5):449–54. https://doi.
org/10.1046/j.1365- 2273.1998.00183.x.
33. Bennett M, Warren F, Jackson GC, Kaylie D. Congenital cholesteatoma: theories, facts,
and 53 patients. Otolaryngol Clin N Am. 2006;39(6):1081–94. https://doi.org/10.1016/j.
otc.2006.08.001.
34. Castle JT. Cholesteatoma pearls: practical points and update. Head Neck Pathol.
2018;12(3):419–29. https://doi.org/10.1007/s12105- 018- 0915- 5.
403

404
35. Tos M.A new pathogenesis of mesotympanic (congenital) cholesteatoma. Laryngoscope.
2000;110(11):1890–7. https://doi.org/10.1097/00005537- 200011000- 00023.
36. Aimi K. Role of the tympanic ring in the pathogenesis of congenital cholesteatoma.
Laryngoscope. 1983;93(9):1140–6. https://doi.org/10.1288/00005537- 198309000- 00005.
37. Koltai PJ, Nelson M, Castellon RJ, Garabedian EN, Triglia JM, Roman S, Roger G.The natural
history of congenital cholesteatoma. Arch Otolaryngol Head Neck Surg. 2002;128(7):804–9.
https://doi.org/10.1001/archotol.128.7.804.
38. Grundfast KM, Ahuja GS, Parisier SC, Culver SM.Delayed diagnosis and fate of congenital
cholesteatoma (keratoma). Arch Otolaryngol Head Neck Surg. 1995;121(8):903–7. https://
doi.org/10.1001/archotol.1995.01890080071014.
39. Darrouzet V, Duclos JY, Portmann D, Bebear JP.Congenital middle ear cholesteatomas in
children: our experience in 34 cases. Otolaryngol Head Neck Surg. 2002;126(1):34–40.
https://doi.org/10.1067/mhn.2002.121514.
40. Miyake S, Miwa T, Yoneda G, etal. Relationship between clinicopathological characteristics
and CYLD expression in patients with cholesteatoma. PLoS One. 2020;15(10):e0240216.
https://doi.org/10.1371/journal.pone.0240216.
41. Basonbul RA, Ronner EA, Kozin ED, Lee DJ, Cohen MS.Systematic review of endoscopic
ear surgery outcomes for pediatric cholesteatoma. Otol Neurotol. 2021;42(1):108–15. https://
doi.org/10.1097/MAO.0000000000002876.
42. von Tröltsch A.The diseases of the ear, their diagnosis and treatment. NewYork: William
Wood & Company; 1864.
43. Wendt H.Desquamative Entzündung des Mittelohres (“Cholesteatom des Felsenbeins”).
Arch Ohr Nasen Kehl-kopfheilk. 1873;14:428–46.
44. Valvassori GE, Mafee MF, Dobben GD.Computerized tomography of the temporal bone.
Laryngoscope. 1982;92(5):562–5. https://doi.org/10.1288/00005537- 198205000- 00018.
45. Manolis EN, Filippou DK, Tsoumakas C, etal. Radiologic evaluation of the ear anatomy
in pediatric cholesteatoma. J Craniofac Surg. 2009;20(3):807–10. https://doi.org/10.1097/
SCS.0b013e318184346e.
46. Friedmann I.The comparative pathology of otitis media, experimental and human. II.The
histopathology of experimental otitis of the Guinea-pig with particular reference to experimental cholesteatoma. J Laryngol Otol. 1955;69(9):588–601.
47. Mudry A, Mlynski R, Kramp B.History of otorhinolaryngology in Germany before 1921.
HNO. 2021;69(5):338–65. https://doi.org/10.1007/s00106- 021- 01046- 9.
48. Habermann J. Zur Entstehung des Cholesteatoms des Mittelohres. Arch Ohrenheilkd.
1888;27:43–51.
49. Dornhoffer JL, Friedman AB, Gluth MB.Management of acquired cholesteatoma in the
pediatric population. Curr Opin Otolaryngol Head Neck Surg. 2013;21(5):440–5. https://doi.
org/10.1097/MOO.0b013e32836464bd.
50. Rüedi L. Pathogenesis and surgical treatment of the middle ear cholesteatoma. Acta
Otolaryngol Suppl. 1979;361:1–45.
51. Sculerati N, Bluestone CD. Pathogenesis of cholesteatoma. Otolaryngol Clin N Am.
1989;22(5):859–68.
52. Tos M, Poulsen G. Attic retractions following secretory otitis. Acta Otolaryngol.
1980;89(5-6):479–86. https://doi.org/10.3109/00016488009127165.
53. Sadé J, Berco E.Atelectasis and secretory otitis media. Ann Otol Rhinol Laryngol. 1976;85(2
Suppl 25 Pt 2):66–72. https://doi.org/10.1177/00034894760850S214.
54. Pace A, Visconti IC, Iannella G, et al. Petrous Bone Cholesteatoma: Facial and
Hearing Preservation. Ear Nose Throat J. 2021;103(6):NP374–81. https://doi.
org/10.1177/01455613211056554.
55. Reddy P, Yan F, Liu YF, McRackan TR, Rizk HG. Hearing preservation in patients who
undergo labyrinthectomy and translabyrinthine procedures: a case report and systematic
review. JAMA Otolaryngol Head Neck Surg. 2020;146(8):741–7. https://doi.org/10.1001/
jamaoto.2020.1292.
M. Tan et al.

19 Cholesteatoma
56. Bartels LJ.Facial nerve and medially invasive petrous bone cholesteatomas. Ann Otol Rhinol
Laryngol. 1991;100(4 Pt 1):308–16. https://doi.org/10.1177/000348949110000408.
57. Sharma SC, Panda S, Thakar A, Devaraja K. Petrous bone cholesteatoma: radical excision with an endeavour for hearing preservation. Indian J Otolaryngol Head Neck Surg.
2019;71(Suppl 2):1572–9. https://doi.org/10.1007/s12070- 019- 01662- 6.
58. Prasad SC, Piras G, Piccirillo E, et al. Surgical strategy and facial nerve outcomes
in petrous bone cholesteatoma. Audiol Neurootol. 2016;21(5):275–85. https://doi.
org/10.1159/000448584.
59. Sudhoff H, Tos M. Pathogenesis of attic cholesteatoma: clinical and immunohistochemical support for combination of retraction theory and proliferation theory. Am J Otol.
2000;21(6):786–92.
60. Tos M, Lau T.Recurrence and the condition of the cavity after surgery for cholesteatoma
using various techniques. Amsterdam: Kugler and Ghedini; 1989.
61. Lange W. Über die Entstehung der Mittelohrcholesteatoma. Z Hals Nas Ohrenheilk.
1925;11:250–71.
62. Bauer JA, Huve FDC, Oliveira FH, Silva MNLD, Sperling N, Costa SSD.Mongolian gerbils as a model for the study of cholesteatoma: otoendoscopic as a diagnostic tool. Int Arch
Otorhinolaryngol. 2022;26(4):e643–8. https://doi.org/10.1055/s- 0041- 1740159.
63. Shinnabe A, Hara M, Hasegawa M, et al. Differences in middle ear ventilation disorders
between pars accida and pars tensa cholesteatoma in sonotubometry and patterns of tympanic and mastoid pneumatization. Otol Neurotol. 2012;33(5):765–8. https://doi.org/10.1097/
MAO.0b013e318254fb85.
64. Abdel Baki F, El Dine MB, El Saiid I, Bakry M. Sinus tympani endoscopic anatomy. Otolaryngol Head Neck Surg. 2002;127(3):158–62. https://doi.org/10.1067/
mhn.2002.127588.
65. Srinivasan V, Banhegyi G, O’Sullivan G, Sherman IW. Pars tensa retraction pockets in
children: treatment by excision and ventilation tube insertion. Clin Otolaryngol Allied Sci.
2000;25(4):253–6. https://doi.org/10.1046/j.1365- 2273.2000.00375.x.
66. Ji C, Zhang X, Yan X, Cao S, Fu T.Cholesteatoma in chronic otitis media secondary to pars
tensa perforation. Acta Otolaryngol. 2023;143(5):376–81. https://doi.org/10.1080/0001648
9.2023.2200437.
67. Shihada R, Brodsky A, Luntz M.Giant cholesteatoma of the temporal bone. Isr Med Assoc
J. 2006;8(10):718–9.
68. Prasad SC, Shin SH, Russo A, Di Trapani G, Sanna M.Current trends in the management of
the complications of chronic otitis media with cholesteatoma. Curr Opin Otolaryngol Head
Neck Surg. 2013;21(5):446–54. https://doi.org/10.1097/MOO.0b013e3283646467.
69. Mustafa A, Heta A, Kastrati B, Dreshaj S. Complications of chronic otitis media
with cholesteatoma during a 10-year period in Kosovo. Eur Arch Otorrinolaringol.
2008;265(12):1477–82. https://doi.org/10.1007/s00405- 008- 0707- 8.
70. Smith JA, Danner CJ.Complications of chronic otitis media and cholesteatoma. Otolaryngol
Clin N Am. 2006;39(6):1237–55. https://doi.org/10.1016/j.otc.2006.09.001.
71. Migirov L, Yakirevitch A, Kronenberg J. Mastoid subperiosteal abscess: a review of 51
cases. Int J Pediatr Otorhinolaryngol. 2005;69(11):1529–33. https://doi.org/10.1016/j.
ijporl.2005.04.009.
72. Pachpande TG, Singh CV.Diagnosis and treatment modalities of cholesteatomas: a review.
Cureus. 2022;14(11):e31153. https://doi.org/10.7759/cureus.31153.
73. Bluestone CD, Klein JO. Intratemporal complications and sequelae of otitis media. In:
Bluestone CD, Casselbrant ML, Stool SE, editors. Pediatric otolaryngology. 4th ed.
Philadelphia, PA: Saunders; 2003. p.687.
74. Ricciardiello F, Cavaliere M, Mesolella M, Iengo M.Notes on the microbiology of cholesteatoma: clinical ndings and treatment. Acta Otorhinolaryngol Ital. 2009;29(4):197–202.
75. Kalcioglu MT, Guldemir D, Unaldi O, Egilmez OK, Celebi B, Durmaz R.Metagenomics
analysis of bacterial population of tympanosclerotic plaques and cholesteatomas. Otolaryngol
Head Neck Surg. 2018;159(4):724–32. https://doi.org/10.1177/0194599818772039.
405

406
76. Akarcay M, Kalcioglu MT, Tuysuz O, Timurlenk E, Guclu H.Ossicular chain erosion in
chronic otitis media patients with cholesteatoma or granulation tissue or without those: analysis of 915 cases. Eur Arch Otorrinolaringol. 2019;276(5):1301–5. https://doi.org/10.1007/
s00405- 019- 05339- 2.
77. Siddiq MA, Hanu-Cernat LM, Irving RM.Facial palsy secondary to cholesteatoma: analysis
of outcome following surgery. J Laryngol Otol. 2007;121(2):114–7. https://doi.org/10.1017/
S0022215106003227.
78. Isaacson G.Diagnosis of pediatric cholesteatoma. Pediatrics. 2007;120(3):603–8. https://doi.
org/10.1542/peds.2007- 0120.
79. Richter GT, Lee KH.Contemporary assessment and management of congenital cholesteatoma. Curr Opin Otolaryngol Head Neck Surg. 2009;17(5):339–45. https://doi.org/10.1097/
MOO.0b013e3283303688.
80. Kalcioglu MT, Kilic O, Tuysuz O, Serier S, Tekin M. Facial canal dehiscence rate:
a retrospective analysis of 372 chronic otitis media cases. Eur Arch Otorrinolaringol.
2019;276(1):79–83. https://doi.org/10.1007/s00405- 018- 5198- 7.
81. Bhutta MF, Williamson IG, Sudhoff HH.Cholesteatoma BMJ. 2011;3(342):d1088. https://
doi.org/10.1136/bmj.d1088.
82. Lela M, Daniele M, Motteo AC, Gahl G.Radiological considerations for endoscopic middle
ear surgery. In: Livio P, Daniele M, editors. Endoscopic ear surgery-principles, indications,
and techniques, vol. 6. 1st ed. NewYork, NY: Thieme; 2014. p.86–1.
83. Muzaffar J, Metcalfe C, Colley S, Coulson C.Diffusion-weighted magnetic resonance imaging for residual and recurrent cholesteatoma: a systematic review and meta-analysis. Clin
Otolaryngol. 2017;42(3):536–43. https://doi.org/10.1111/coa.12762.
84. Jindal M, Riskalla A, Jiang D, Connor S, O’Connor AF.A systematic review of diffusionweighted magnetic resonance imaging in the assessment of postoperative cholesteatoma.
Otol Neurotol. 2011;32(8):1243–9. https://doi.org/10.1097/MAO.0b013e31822e938d.
85. Venail F, Bonafe A, Poirrier V, Mondain M, Uziel A.Comparison of echo-planar diffusion-weighted imaging and delayed postcontrast T1-weighted MR imaging for the detection of residual cholesteatoma. AJNR Am J Neuroradiol. 2008;29(7):1363–8. https://doi.
org/10.3174/ajnr.A1100.
86. Gaurano JL, Joharjy IA.Middle ear cholesteatoma: characteristic CT ndings in 64 patients.
Ann Saudi Med. 2004;24(6):442–7. https://doi.org/10.5144/0256- 4947.2004.442.
87. Profant M, Sláviková K, Kabátová Z, Slezák P, Waczulíková I. Predictive validity of MRI
in detecting and following cholesteatoma. Eur Arch Otorrinolaringol. 2012;269(3):757–65.
https://doi.org/10.1007/s00405- 011- 1706- 8.
88. Li PM, Linos E, Gurgel RK, Fischbein NJ, Blevins NH.Evaluating the utility of non-echoplanar diffusion-weighted imaging in the preoperative evaluation of cholesteatoma: a metaanalysis. Laryngoscope. 2013;123(5):1247–50. https://doi.org/10.1002/lary.23759.
89. Garcia-Iza L, Guisasola A, Ugarte A, Navarro JJ, Goiburu M, Altuna X.Utility of diffusionweighted magnetic resonance imaging in the diagnosis of cholesteatoma and the inuence of
the learning curve. Eur Arch Otorrinolaringol. 2018;275(9):2227–35. https://doi.org/10.1007/
s00405- 018- 5074- 5.
90. Dhepnorrarat RC, Wood B, Rajan GP.Postoperative non-echo-planar diffusion-weighted
magnetic resonance imaging changes after cholesteatoma surgery: implications for
cholesteatoma screening. Otol Neurotol. 2009;30(1):54–8. https://doi.org/10.1097/
MAO.0b013e31818edf4a.
91. Akkari M, Gabrillargues J, Saroul N, et al. Contribution of magnetic resonance imaging to the diagnosis of middle ear cholesteatoma: analysis of a series of 97 cases. Eur
Ann Otorhinolaryngol Head Neck Dis. 2014;131(3):153–8. https://doi.org/10.1016/j.
anorl.2013.08.002.
92. Laske RD, Roth TN, Baráth K, Schuknecht B, Huber AM, Röösli C.The Role of NonEchoplanar Diffusion-Weighted Magnetic Resonance Imaging in Diagnosis of Primary
Cholesteatoma and Cholesteatoma Recidivism as an Adjunct to Clinical Evaluation. Ann
Otol Rhinol Laryngol. 2018;127(12):919–25. https://doi.org/10.1177/0003489418800833.
M. Tan et al.

19 Cholesteatoma
93. De Foer B, Vercruysse JP, Bernaerts A, etal. Detection of postoperative residual cholesteatoma with non-echo-planar diffusion-weighted magnetic resonance imaging. Otol Neurotol.
2008;29(4):513–7. https://doi.org/10.1097/MAO.0b013e31816c7c3b.
94. Sun WH, Fan JK, Huang TC.The efcacy of DW and T1-W MRI combined with CT in
the preoperative evaluation of cholesteatoma. J Pers Med. 2022;12(8):1349. https://doi.
org/10.3390/jpm12081349.
95. Bakaj T, Zbrozkova LB, Salzman R, Tedla M, Starek I.Recidivous cholesteatoma: DWI MR
after canal wall up and canal wall down mastoidectomy. Bratisl Lek Listy. 2016;117(9):515–20.
https://doi.org/10.4149/bll_2016_100.
96. Migirov L, Tal S, Eyal A, Kronenberg J.MRI, not CT, to rule out recurrent cholesteatoma and
avoid unnecessary second-look mastoidectomy. Isr Med Assoc J. 2009;11(3):144–6.
97. Patel B, Hall A, Lingam R, Singh A. Using non-echoplanar diffusion weighted MRI in
detecting cholesteatoma following canal wall down mastoidectomy– our experience with 20
patient episodes. J Int Adv Otol. 2018;14(2):263–6. https://doi.org/10.5152/iao.2018.5033.
98. Colletti V. Multifrequency tympanometry. Audiology. 1977;16(4):278–87. https://doi.
org/10.3109/00206097709071839.
99. Jeng FC, Tsai MH, Brown CJ. Relationship of preoperative ndings and ossicular discontinuity in chronic otitis media. Otol Neurotol. 2003;24(1):29–32. https://doi.
org/10.1097/00129492- 200301000- 00007.
100. Han SY, Lee DY, Chung J, Kim YH.Comparison of endoscopic and microscopic ear surgery in pediatric patients: a meta-analysis. Laryngoscope. 2019;129(6):1444–52. https://doi.
org/10.1002/lary.27556.
101. Karmarkar S, Bhatia S, Saleh E, etal. Cholesteatoma surgery: the individualized technique. Ann
Otol Rhinol Laryngol. 1995;104(8):591–5. https://doi.org/10.1177/000348949510400801.
102. Kalcioglu MT, Ozerk A, Egilmez OK, et al. Mastoid cavity obliteration with cartilage
graft; evaluation of 35 patients. Medeni Med J. 2019;34(4):360–7. https://doi.org/10.5222/
MMJ.2019.60948.
103. Kokten N, Tuysuz O, Zenginkinet T, Hanege FM, Kalcioglu MT.Inhibitory effect of mesna
and 5-uorouracil on propylene glycol-induced cholesteatoma in rats. Acta Otorhinolaryngol
Ital. 2021;41(5):481–6. https://doi.org/10.14639/0392- 100X- N1392.
104. Vincenti V, Magnan J, Saccardi MS, Zini C.Chemically assisted dissection by means of mesna
in cholesteatoma surgery. Otol Neurotol. 2014;35(10):1819–24. https://doi.org/10.1097/
MAO.0000000000000514.
105. Bovi C, Luchena A, Bivona R, Borsetto D, Creber N, Danesi G.Recurrence in cholesteatoma
surgery: what have we learnt and where are we going? A narrative review Acta Otorhinolaryngol
Ital. 2023;43(Suppl 1):S48–55. https://doi.org/10.14639/0392- 100X- suppl.1- 43- 2023- 06.
106. Kalcioglu MT, Cicek MT, Bayindir T, Ozdamar OI.Effectiveness of MESNA on the success
of cholesteatoma surgery. Am J Otolaryngol. 2014;35(3):357–61. https://doi.org/10.1016/j.
amjoto.2014.01.002.
107. Kalcioglu MT, Bayazit YA.Does MESNA application make sense in chronic otitis media surgery? Am J Otolaryngol. 2014;35(5):687–8. https://doi.org/10.1016/j.amjoto.2014.06.008.
108. Wright CG, Bird LL, Meyerhoff WL. Effect of 5-uorouracil in cholesteatoma development in an animal model. Am J Otolaryngol. 1991;12(3):133–8. https://doi.
org/10.1016/0196- 0709(91)90142- 3.
109. Eğilmez OK, Kökten N, Baran M, Kalcioglu MT, Doğan Ekici I, Tekin M.Electrophysiological
and histopathological evaluation of effects of Sodium-2 mercaptoethanesulfonate used for
middle ear surgery on facial nerve functions. J Int Adv Otol. 2018;14(2):239–44. https://doi.
org/10.5152/iao.2017.3888.
110. Vincenti V, Magnan J, Zini C.Cochlear effects of intraoperative use of Mesna in cholesteatoma surgery. Acta Biomed. 2014;85(1):30–4.
407
Соседние файлы в папке Библиотека им академика М.И. Перельмана
