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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5184_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Foreword
- •Foreword
- •Foreword
- •Past Presidents of the AACP
- •Previous Haden-Stack Award Recipients
- •Some Additional History on TMD and Movement Disorders, Recollections from Dr. Stack …
- •Preface
- •Acknowledgments
- •1 Introduction
- •2 Embryology
- •Contents
- •5.2 Soft Tissue Components
- •6 Summary
- •References
- •1 Introduction
- •2.3 Orthopedic Instability
- •2.5 Conclusion
- •4 Trauma
- •4.1 Indirect Trauma
- •4.2 Direct Trauma
- •5 Parafunctional Activities
- •8 Genetics
- •9 Conclusion
- •References
- •1 Introduction
- •2 Historical Perspective
- •3 Evidence-Based Perspective
- •3.3.1 Class II Treatment
- •3.3.2 Class III Treatment
- •3.5 Functional Occlusion
- •3.6 Occlusal Appliance Therapy
- •3.7 Psychosocial Considerations
- •4 Diagnosis: TMJ Sounds
- •5 The OPPERA Study
- •5.1 Rationale
- •5.3 Results
- •7 Conclusion
- •Suggested Readings
- •1 Introduction
- •2 Pain Is Protective
- •4 The Many Faces of Chronic Orofacial Pain
- •6 Episodic Neuropathic Pain
- •6.1 Trigeminal Neuralgia
- •6.2 Glossopharyngeal Neuralgia
- •7.4 Preventing PTTN
- •8.1 Persistent Idiopathic Dentoalveolar Pain
- •8.2 Diagnostic Criteria
- •8.4 Continuous Neuropathic Orofacial Pain
- •8.4.1 Burning Mouth Syndrome
- •8.5 Management
- •9 Summary
- •Suggested Readings
- •1 Introduction
- •3.2 TMJ Internal Derangements
- •Joint Fluid
- •3.2.2 Subluxation
- •3.2.3 Disc Adhesion
- •3.2.5 Degenerative Joint Disease
- •Rheumatoid Arthritis
- •Imaging
- •Synovial Chondromatosis
- •Imaging
- •4 Summary
- •Suggested Readings
- •3.1.1 Advantages
- •3.1.2 Limitations
- •3.2.1 TMJ Dislocation
- •Symptoms
- •3.2.3 TMJ Fractures
- •Symptoms
- •4.2 Disc Displacement
- •4.3 Pseudo-Disc
- •4.4 Stuck Disc
- •4.5 Perforated Disc
- •4.9 Hypermobility
- •4.10 Ankylosis
- •6 TMJ Arthritis
- •6.1 Degenerative Disease (Osteoarthritis)
- •6.2.1 Juvenile Idiopathic Arthritis
- •6.2.2 Rheumatoid Arthritis
- •6.4 Infectious Arthritis
- •6.5 Idiopathic Condylar Resorption
- •7 Summary
- •Appendix. MRI Protocols
- •References
- •16 Initial Consultation
- •17 Pain
- •17.1 Primary Joint Pain
- •1 Introduction
- •2 Patient Education
- •3 Avoidance Therapy
- •4 Psychological Factors
- •5 Obstructive Sleep Apnea
- •6 Examination
- •7 Thermal Application
- •8 Pharmacologic Management
- •9 Physical Therapy
- •10 Acupuncture
- •12 Injections
- •13 Chronic Pain Management
- •14 Referrals
- •15 Surgical Management
- •17.2 Primary Muscle Pain
- •17.3 Open Lock (TMJ Dislocation)
- •18 Summary
- •References
- •1 Introduction
- •5 TMJ Arthrotomy
- •5.1 Discectomy
- •5.2 Disc Repositioning
- •5.3 Arthroplasty
- •6.1 Joint Prostheses
- •6.2 Autogenous TMJR
- •7 Summary
- •Suggested Readings
- •1 Introduction
- •1.1 Internal derangement of TMJ
- •2 Techniques
- •3 Preparation
- •4 Procedure
- •5 Additives
- •6 Clinical Pearls
- •7 Complications
- •8 Post-op Care
- •References
- •1 Introduction
- •2.1 The Trigeminal Nuclei
- •4 Temporomandibular Joint (TMJ)
- •4.1 Growth Disorders
- •4.2 Arthritic Disease
- •4.3 Infectious Arthritis
- •4.4 Traumatic Arthritis
- •4.5 Rheumatoid Arthritis
- •6 Movement Disorders
- •6.2 Hypokinetic Movement Disorders
- •7 Dystonia
- •7.1.1 Cervical Dystonia
- •7.1.2 Oromandibular Dystonia (OMD)
- •7.1.3 Limb Dystonia (LD)
- •7.1.4 Restless Leg Syndrome (RLS)
- •8 Tremor
- •8.1 Paroxysmal Kinesigenic Dyskinesia (PKD)
- •8.2 Parkinsonism
- •8.3 Tourette Syndrome and/or Tic Disorder
- •8.4 PANS
- •8.5 PANDAS
- •10 Summary
- •Suggested Reading
- •1 Introduction
- •2 Pain
- •3 Training
- •4.1 Panoramic Radiograph
- •4.2 TMJ Plain Films
- •4.3 Clinical Documentation
- •4.4.1 Intraoral photographs
- •5 Summary
- •Suggested Readings
- •1 Introduction
- •3 Greenstick Fractures
- •5 Summary
- •Suggested Readings
- •TMJ Pathology Treatment
- •1 Introduction
- •2 Case 1
- •2.2 Case Report
- •3 Case 2
- •3.2 Case Report
- •4 Case 3
- •5 Case 4
- •6 Summary
- •Suggested Readings
- •1 Introduction
- •2 Dystonias
- •2.1 Blepharospasm
- •2.1.1 Case 1
- •2.1.2 Case 2
- •2.2 Torticollis
- •2.2.1 Case 3
- •2.2.2 Case 4
- •2.3 Gait Disorders
- •2.3.1 Typical Gait Disorders
- •Hemiplegic Gait
- •Diplegic Gait
- •Myopathic Gait
- •Ataxic Gait
- •Parkinsonian Gait
- •Neuropathic Gait
- •2.3.2 Other Gait Disorders
- •2.3.3 Case 5
- •2.3.4 Case 6
- •2.4 Paroxysmal Kinesigenic Dyskinesia (PKD)
- •2.4.1 Case 7
- •2.4.2 Case 8
- •2.5 Parkinsonism
- •2.5.2 Case 9
- •2.6.1 Case 10
- •2.6.2 Case 11
- •2.7 Tourette Syndrome
- •2.8 TS Diagnosis
- •2.9 Treating TS
- •2.9.1 Case 12
- •2.9.2 Case 13
- •2.9.3 Case 14
- •3 Summary
- •Suggested Readings

Temporomandibular Joint: Review of the Anatomy, Pathology, and Magnetic Resonance Imaging…
111
coma, and metastatic tumors. In chondrosarcoma, MRI typically shows a lobulated mass
with heterogeneous signal intensity on T1- and
T2-weighted images. The mass is usually
hypointense on T1-weighted images and hyperintense on T2-weighted images. In osteosarcoma, MRI typically shows a large, lobulated
mass with heterogeneous signal intensity on T1and T2-weighted images. The mass is usually
hypointense on T1-weighted images and hyperintense on T2-weighted images. In metastatic
tumors, MRI typically shows a mass with heterogeneous signal intensity and variable
enhancement [1].
5.3 MR inEvaluation ofTumor
Extent
MRI is valuable in the evaluation of tumor extent
and involvement of adjacent structures. It can
help to determine the involvement of the condyle, articular disc, and adjacent soft tissue
structures. MRI can also help to identify the
presence of metastases in adjacent bones and
soft tissues [50].
5.4 MR inTreatment Planning
MRI is useful in treatment planning for tumors
and tumorlike conditions of the TMJ.It can help
to determine the extent of surgical resection and
to plan for reconstruction of the TMJ.MRI can
also help to guide biopsy and to monitor response
to therapy [50].
MRI is a valuable tool in the evaluation of
tumors and tumorlike conditions of the TMJ.It
provides excellent soft tissue contrast and multiplanar imaging capabilities, which make it useful
in the diagnosis and management of these conditions. MRI can help to determine the extent of
disease, involvement of adjacent structures, and
response to therapy. Further research is needed to
improve our understanding of the role of MRI in
the diagnosis and management of tumors and
tumorlike conditions of the TMJ [25, 26].
6 TMJ Arthritis
The TMJ, like other synovial joints in the body, is
susceptible to various inammatory arthritic conditions. In addition to degenerative arthritis,
which is a common occurrence in the TMJ,
arthritis resulting from crystalline deposition diseases is also prevalent. Furthermore, TMJ arthritis can be secondary to infection or trauma. It is
important to discuss arthritis of the TMJ based on
the underlying pathophysiological mechanisms
involved in its development. By understanding
the specic mechanisms at play, clinicians can
better diagnose, treat, and manage TMJ arthritis
to alleviate symptoms and improve the overall
function of the joint [24, 27].
6.1 Degenerative Disease (Osteoarthritis)
Osteoarthritis (OA) is a chronic degenerative disease that primarily affects the articular cartilage
of synovial joints. It involves the remodeling of
the underlying subchondral bone and can also
affect the synovium. Among all joint pathologies,
TMJ is commonly affected by osteoarthritis.
Interestingly, there is often a discrepancy between
radiographic evidence of OA and presence of
symptoms, a classic phenomenon in OA, known
as clinical-radiological dissociation. Populationbased studies have shown that up to 35% of
asymptomatic individuals exhibit minimal condylar attening on radiographs, while approximately 11% of patients experience TMJ
symptoms related to OA [51].
The most prevalent symptom of TMJ OA is
pain during chewing. Typically, the pain originates from the periarticular soft tissues and masticator muscles, which can be in a protective reex
spasm. Other common symptoms include masticator muscle fatigue, trismus (limited mouth
opening), decreased range of motion, difculty
opening the mouth, and joint crepitations [9, 20].
Radiographically, TMJ OA is characterized by
specic features such as irregularities in the cortical
bone of the articular surface, erosion, and formation

112
F. A. Chagas-Neto et al.
of osteophytes (Fig. 21). Erosion refers to focal
areas of decreased density along the cortical margin
of the mandibular condyle’s articular surface and
the subchondral region (Fig. 22). Osteophyte formation usually occurs in the later stages of the dis-
ease and is an attempt by the joint to stabilize and
increase its surface area to better withstand axial
loading forces. Various imaging modalities have
been utilized to assess TMJ OA, with CT and MRI
being the most indicated [24, 51].
ab
Fig. 21 Degenerative changes. Coronal (a) and sagittal
reformation (b) of multislice computed tomography (CT)
demonstrates deformity and osteophytosis of the mandib-
ular condyle (c), subchondral sclerosis of the mandibular
condyle and of the articular eminence (a), and asymmetrical loss of joint space
ab
Fig. 22 Degenerative changes. Coronal proton densityweighted (a) and (b) and sagittal T1-weighted (c) magnetic resonance imaging (MRI) of three different patients
demonstrates sclerosis and osteophytosis of the mandibular condyle (c), subchondral cysts (arrowheads in b) of the
mandibular condyle, and loss of joint space
c

Temporomandibular Joint: Review of the Anatomy, Pathology, and Magnetic Resonance Imaging…
113
6.2 Inammatory Arthritis
6.2.1 Juvenile Idiopathic Arthritis
Juvenile idiopathic arthritis (JIA) is the most
prevalent rheumatic disease in childhood, affecting girls more frequently than boys. The condition primarily affects synovial joints, and its
onset typically occurs in two peaks: the rst
between 1 and 3 years of age, and the second
between 8 and 12 years. TMJ involvement is
observed in 17–87% of JIA patients. JIA can
manifest as systemic, polyarticular, or periarticular forms, with the TMJ being more commonly
affected in those with polyarticular joint involvement. Symptoms of TMJ involvement in JIA
often include pain, joint tenderness, crepitation,
stiffness, and reduced range of motion. In some
cases, late-stage disease may lead to the development of bony ankylosis [49, 52, 53].
Various imaging techniques such as orthopantomography, CT, MRI, and ultrasound have been
utilized to evaluate TMJ involvement in
JIA. Orthopantomography and CT are particularly useful in detecting bony erosions secondary
to TMJ arthritis, but they involve radiation exposure, which can be a concern in young patients.
MRI and ultrasound have gained popularity in
assessing TMJ involvement in JIA due to their
superior soft tissue resolution and the absence of
ionizing radiation. These techniques allow for
earlier diagnosis of TMJ arthritis without compromising patient safety. Acute TMJ arthritis
typically presents with joint effusion and synovial thickening, which are visible on T2-weighted
MRI images, without apparent bony changes.
However, it is important to note that joint or periarticular tissue enhancement is not a specic sign
of acute TMJ arthritis, as abnormal enhancement
can also be observed in healthy individuals.
Evaluation of condylar resorption, which suggests a more chronic TMJ arthritis, is better
achieved using nonfat-suppressed T1-weighted
sequences [52–55].
6.2.2 Rheumatoid Arthritis
Rheumatoid arthritis (RA) is a chronic inammatory condition primarily affecting periarticular
tissues such as the synovial membrane, joint cap-
sules, tendons, tendon sheaths, and ligaments.
Involvement of the internal joint structures occurs
as a secondary effect. The prevalence of RA in
the general population is approximately 2–2.5%,
with a higher incidence among females. The typical age of onset is between 40 and 60years, and
TMJ involvement is observed in approximately
50–75% of patients with RA [54, 56, 57].
RA is a slowly progressive disease with an
insidious onset, leading to the gradual destruction of articular and periarticular soft tissues and
adjacent bones, ultimately resulting in joint
deformity. TMJ involvement typically occurs at a
later stage of the disease (Fig.23). Symptoms of
TMJ involvement in RA include deep, dull aching pain in the preauricular area particularly during chewing, as well as limited range of motion
and morning stiffness. As the disease progresses,
there is gradual resorption of the mandibular condyle [27, 58, 59].
Radiographically, RA is characterized by specic features such as loss of joint space, destruction of the condyle, attening with anterior
positioning of the condyle, attening of the articular eminence, and erosion of the glenoid fossa.
One distinguishing factor of RA is the presence of
synovial proliferation, which is an early pathological process and can be visualized on MRI.Synovial
proliferation is a consistent nding in all patients
with RA and helps differentiate it from other types
of arthritis. Additionally, joint effusion is relatively
common in RA cases and can be detected through
imaging examinations [24, 56–59].
6.3 Metabolic Arthritis/Crystalline
Arthropathies
Calcium pyrophosphate dihydrate deposition disease (CPPD) is a metabolic arthropathy characterized by the accumulation of calcium
pyrophosphate dihydrate crystals in and around
joints, particularly in the articular and brocartilage. TMJ involvement in CPPD can range from
asymptomatic calcication of the disc to signicant joint destruction with erosive changes in the
mandibular condyle and adjacent skull base.
Common symptoms include pain, swelling in the

114
cd
F. A. Chagas-Neto et al.
ab
Fig. 23 Coronal proton density-weighted (a), sagittal
proton density-weighted (b), and sagittal T1-weighted (c)
magnetic resonance imaging (MRI) and sagittal reformation (d) of multislice computed tomography (CT) of the
same patient demonstrate erosions (arrowheads) of the
preauricular area, and occasional hearing loss.
Pain can be aggravated by chewing. Less common symptoms may include TMJ clicking, tinnitus, and malocclusion [60].
The radiographic appearance of CPPD can
vary. Computed tomography (CT) reveals calcium deposits in the disc or periarticular tissues.
On MRI, CPP deposits typically appear as areas
of decreased signal intensity on both T1- and
glenoid fossa (g) and of the mandibular condyle (c). There
is also synovial proliferation (arrow in a and b) in the joint
space, associated with bone marrow edema in the mandibular condyle (c)
T2-weighted sequences (Fig. 24). CT and MRI
also show erosions near the condyle and fossa,
accompanied by adjacent CPPD deposits. These
erosions can extend into the skull base and middle cranial fossa. Involvement of other joints with
chondrocalcinosis can provide clues for the diagnosis. Differential diagnoses to consider include
synovial chondromatosis, synovial osteochondroma, and osteosarcoma [46, 54].

ab
cd
Temporomandibular Joint: Review of the Anatomy, Pathology, and Magnetic Resonance Imaging…
115
Fig. 24 Coronal proton density-weighted (a), sagittal
proton density-weighted (b), sagittal T1-weighted (c), and
sagittal T1-weighted FAT SAT post-endovenous gadolinium injection magnetic resonance imaging (MRI) of the
same patient demonstrates joint distension with uid and
6.4 Infectious Arthritis
multiple small foci with low signal intensity in all
sequences, compatible with calcications (arrowheads).
There is also exuberant synovitis (arrows in d), depicted
in the post-contrast image. Mandibular condyle (c)
systems and concurrent systemic conditions
such as diabetes mellitus, rheumatoid arthriInfections of the TMJ typically occur as a result
of the direct spread of infection from nearby tissues into the joint space. Another important
mechanism is direct contamination of the articular space, after joint injections. While relatively
rare, systemic infections like tuberculosis and
syphilis can also affect the TMJ [25].
TMJ infection is more commonly observed
in individuals with compromised immune
tis, or a history of intravenous drug use. These
factors increase the susceptibility to TMJ
infection and can contribute to the severity
and complications associated with the
condition.
Therefore, it is crucial to consider these underlying factors when evaluating and managing TMJ
infections to ensure appropriate treatment and
prevent further complications [54].

116
F. A. Chagas-Neto et al.
6.5 Idiopathic Condylar Resorption
Idiopathic condylar resorption (ICR), also known
as progressive condylar resorption or condylar
atrophy, is a rare and perplexing condition that primarily affects the TMJ.ICR is characterized by
the progressive resorption of the condylar head,
leading to signicant mandibular deformities and
functional disturbances. The etiology of ICR
remains unclear, as the condition occurs spontaneously without any apparent triggering factors or
underlying systemic diseases. This idiopathic
nature makes the diagnosis and treatment of ICR
particularly challenging for clinicians [61–63].
ICR typically affects females in their late
teens or early adulthood and often presents
unilaterally, although bilateral involvement
can occur. Patients with ICR may initially
complain of mild symptoms such as clicking or
popping in the TMJ, joint pain, or limited jaw
movement. However, as the condition progresses, patients may experience facial asymmetry, malocclusion, and severe TMJ
dysfunction [61, 64].
The radiographic ndings typically demonstrate progressive condylar resorption, with the
condylar head gradually diminishing in size and
shape, leading to a loss of condylar height and
structural integrity (Fig.25) [62–64].

Temporomandibular Joint: Review of the Anatomy, Pathology, and Magnetic Resonance Imaging…
117
a
c
b
d
Fig. 25 Coronal proton density-weighted (a, c) and sag-
ittal proton density-weighted (b, d) magnetic resonance
imaging (MRI) of the same patient demonstrates normal-
sized mandibular condyle (c) in (a) and (b) and typical
ndings of idiopathic condylar resorption in (c) and (d)

118
F. A. Chagas-Neto et al.
7 Summary
TMJ disorders are a heterogeneous group of
conditions that can affect the articular, muscular,
and/or ligamentous components of the joint. The
most common symptoms include pain, restricted
movement, joint noises, and muscle tenderness,
which can signicantly impact the quality of life
of affected individuals. Although the etiology of
TMJ disorders is not fully understood, several
factors have been implicated in their pathogenesis, including trauma, malocclusion, parafunc-
tional habits, and systemic diseases such as
rheumatoid arthritis. MRI is an imaging modality that is commonly used for TMJ evaluation,
especially for assessing the soft tissue components of the joint. MRI is highly sensitive for
detecting disc displacement and other soft tissue
abnormalities such as joint effusion, synovitis,
and muscle edema. Moreover, MRI can provide
information about the blood ow and perfusion
of the joint, which can be useful for differentiating between inammatory and noninammatory
conditions.

Temporomandibular Joint: Review of the Anatomy, Pathology, and Magnetic Resonance Imaging…
Appendix. MRI Protocols
Plane Sequence Slice thickness TR TE FOV Mouth position
Axial T1 2mm 350 Minimal 250 Closed
Coronal (oblique) T1 2mm 350 Minimal 100 Closed
Sagittal (oblique) PD 2mm 1500 (350) Minimal 100 Closed
Sagittal (oblique) PD 2mm 1500 (350) Minimal 100 Open
Sagittal (oblique) T2 2mm 2500 70 100 Closed
Plane Sequence Slice thickness TR TE FOV Mouth position
Coronal T1 3mm 500 Minimal 250 Closed
Axial T1 2mm 500 Minimal 250 Closed
Left sagittal oblique T2 and PD 3500 Minimal 100 Closed
Right sagittal oblique T2 and PD 3500 Minimal 100 Closed
Left sagittal oblique T2 and PD 3500 Minimal 100 Open
Right sagittal oblique T2 and PD 3500 Minimal 100 Open
Left sagittal oblique T2 1180 64 100 Dynamic
Right sagittal oblique T2 1180 64 100 Dynamic
Plane Sequence Slice thickness TR TE FOV Mouth position
Axial T1 5mm 300 12 250 Closed
Coronal (oblique) T1 2mm 400–500 10–20 100 Closed
Sagittal (oblique) T2 2mm 2600 120 100 Closed
Sagittal (oblique) PD 2mm 2000 10–14 100 Open
Sagittal (oblique) T2 GRE 2mm 600 15 100 Closed
Sagittal SSFSE PD 3.5mm 88 12 150 Dynamic
Plane Sequence Slice thickness TR TE FOV Mouth position
Coronal (oblique) T1 3mm 300 11 150 Closed
Coronal (oblique) PD 3mm 2000 21 150 Closed
Sagittal (oblique) PD 3mm 2300 11 150 Closed
Sagittal (oblique) T2 TSE FS 3mm 4500 78 150 Closed
Coronal (oblique) PD 3mm 2000 20 150 Open
Sagittal (oblique) PD 3mm 2300 11 150 Open
Sagittal (oblique) T2 TSE FS 3mm 4500 78 150 Open
Plane Sequence Slice thickness TR TE FOV Mouth position
Axial T1 2mm 500 Minimal 250 Closed
Coronal (oblique) T1 3mm 500 Minimal 100 Closed
Bilateral sagittal oblique T2 and PD 3mm 3500 Minimal and 85 100 Closed and open
Bilateral sagittal oblique T2 3mm 1180–2000 64 100 Dynamic cine
119
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