Orofacial Manifestations of CT disease & Radiation Part 2 Flashcards
1
Q
Sjogren Syndrome: General
A
- autoimmune disease
- Chronic inflammation of exocrine glands
- lacrimal and salivary glands
- Lymphocyte infiltrate
- replaces fxnal epithelium
- Females
- Enlarge major salivary gland
- Parotid Gland
- 5% develop B-Cell Lymphoma
2
Q
Sjogren Syndrome: Clinical Manifestations
A
- Keratoconjunctivitis sicca
- hyposalivation
- xerotrachea
- Dry vagina
3
Q
Sjogren Syndrome: Classification
A
- Primary SS
- keratoconjunctivitis sicca
- salivary gland dysfxn (hyposalivation)
- Secondary SS
- secondary to other autoimmune diseases
- ex: RA, SLE, scleroderma, polymyositis
- secondary to other autoimmune diseases
4
Q
Primary Sjogren Syndrome Criteria
A
- (+) Anti-SSA/Ro antibody (Score=3)
- Focal lymphocytic sialadenitis (Score=3)
- w/focus score ≥ 1 foci/4 mm2 (Score=1)
- Abnormal ocular staining ≥ 5 (Score=1)
- Schirmers test ≤ 5 mm/5 minutes (Score=1)
- Unstimulated salivary flow rate ≤ 0.1 ml/minute (Score=1)
Total Score of ≥ 4 = Primary SS
5
Q
Sjogren Syndrome: Oral Manifestations
A
- Xerostomia w/burning sensation on tongue
- common
- Difficulty eating dry foods
- sensitive to acidic and spicy foods
- altered taste
- coughing episodes
- speech disturbances
- increase caries risk
- oral prosthesis difficulty
- Candidiasis
- may affect taste and cause burning sensation
6
Q
Sjogren Syndrome: Headaches
A
- Migraines mostly
- Might be linked to Raynaud’s phenomenon
7
Q
Sjogren’s Syndrome: Salivary Gland
A
- Parotid Gland swelling:
- 30-40 % tenderness or pain when eating
- Complication:
- lymphoid tissue lymphoma
8
Q
Systemic Sclerosis (SSc)
A
- Aka Scleroderma
- Multisystem CT disorder
- Abnormal Fibrosis
- dysfxn of skin, vasculature, internal organs
- 3 Types:
- Diffuse
- Limited
- Localized
- Females
- African Americans
- more common
- greater severity
- African Americans
9
Q
Systemic Sclerosis: criteria
A
- Finger Skin thickening
- extends proximal to metacarpopha-langeal joint
OR→ 7 additive items
- Skin thickening of fingers
- Fingertip lesions
- Telangiectasia
- Abnormal Nail fold capillaries
- Interstitial lung disease
- or pulmonary arterial hypertension
- Raynaud’s phenomenon
- SSc-related autoantibodies
10
Q
Diffuse Systemic Sclerosis
A
- Cutaneous disease of:
- face
- neck
- trunk
- proximal & distal parts of limbs
- Functional changes in:
- Lungs
- Kidneys
11
Q
Limited Systemic Sclerosis
A
- CREST Syndrome
- thickening of the skin on
- Face
- Neck
- Distal part of limbs
- CREST:
- Calcinosis
- Raynaud’s Phenomenon
- Esophageal dysmotility
- sclerodactyly
- Telanglectasias
- thickening of the skin on
12
Q
Localized Systemic Sclerosis
A
- Morphea
- localized scleroderma
- involves the:
- skin
- subcutaneous tissue
- muscle
- No systemic manifestation
13
Q
Systemic Sclerosis: Eitology
A
- Unknown
- Abnormal and excessive fibrosis→ All cases
- leads to:
- end-organ structural damage
- dysfunction
- leads to:
14
Q
Systemic Sclerosis: Oral manifestations
A
- Microstomia
- limited mouth opening due to fibrosis
- Mucogingival problems
- Fibrosis of:
- hard palate
- soft palate
- tongue
- Telangiectasis
- Pigmentation of facial skin and oral mucous membranes
- Dry Mouth (Hyposalivation)
- Dry eyes
- Widened PDL space
- TMJ dysfunction
- Trigeminal Neuropathy
- ⇡ Dental Caries
- hyposalivation
- restricted mouth opening
- ⇡ PD & gingival scores
- obliterative microvasculopathy
15
Q
Systemic Sclerosis: TMJ
A
- TMJ Dysfxn
- Bone resorption or erosion of:
- coronoid process
- condyle
- angle the mandible
- Ramus
- Fibrosis of: (-→ Limited ROM)
- masticatory m.
- Facial expression m.
- oral and peri oral tissues
- Bone resorption or erosion of:
- Clinical Presentation:
- articular pain and swelling
- due to tendonitis and synovitis
- articular pain and swelling
- Radiographic changes:
- angle of mandible resorption