Joint disease/arthritis Flashcards

1
Q

Outline types of joints

A

Joints are connections between bones
–Synovial joints- movable joints of the body
(knee joint)
–Non synovial joints- structural integrity and minimal movement
•Cartilaginous (e.g., intervertebral disks)
•Fibrous (e.g., cranial sutures)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

List structures of synovial joints

A

Articular surface is covered by hyaline cartilage (Healing is poor)
–Articular cartilage: acts as a shock absorber between bones
•Chondrocytes produce the matrix + enzymes and cytokines to degrade it
•Collagen II
•Proteoglycans
•H2O

  • Joint capsule (pain sensitive) lined by synovium
  • Ligaments- band of fibrous connective tissue
  • Bursa- fibrous sac that acts as a cushion to ease movement in areas that are subject to friction
  • Synovial membrane and synovial fluid
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Describe synovium

A

The synovium aka synovial membrane lacks a basement membrane-> quick exchange between blood and synovium
–Type A synovial cells are macrophage-like (phagocytic and produce hyaluronic acid)
–Type B synovial cells (fibroblast-like)->protein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe synovial fluid

A

Synovial fluid located in synovial cavity (lubrication and nourishment for cartilage)

  • Colour - colourless to pale yellow
  • Clarity- transparent
  • WBC/mm3 < 200
  • PMNs < 25%
  • Glucose nearly equal to blood
  • Gram stain negative
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Classify arthritis

A
  • Osteoarthritis
  • Arthritis related to infectious agents
  • Arthritis related to immunological disease
  • Arthritis induced by crystals
  • Arthritis associated with systemic disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Osteoarthritis

A

most common type of rheumatic disease
Degenerative disease characterised by progressive erosion of articular cartilage affecting 80% of elderly
classified as primary or secondary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Non inflammatory process of arthritis

A

osteoarthrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Define primary osteoarthritis

A

•Primary (idiopathic)
–Affects elderly
–Involves the weight-bearing joints (e.g., hips and knees)
•More common in overweight
–Interphalangeal joints
–Some families have mandelian pattern of inheritance of primary generalised osteoathritis (mutation in the gene for type II collagen)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Define secondary osteoarthritis

A
•Develop at any age in a damaged joint
–Trauma
–Rheumatoid arthritis
–Gout
–Tuberculosis
–Acromegaly
–Haemochromatosis
–Deformity (e.g., dislocation of the hip)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

PATHOGENESIS OF OSTEOARTHRITIS

A

•Aging and mechanical effects “wear and tear”
•Biomechanical stresses of weight bearing over time
•Genetic factors
•Changes in the composition and the mechanical properties of cartilage
–Increased water and decreased concentration of proteoglycans
–Chondrocytes produce IL1, TNF-α and nitric oxide
•Stimulate production of metalloproteinase that degrade the matrix
•Inhibit production of type II collagen and proteoglycan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Morphology of osteoarthritis

A

Destruction of articular cartilage
–Chondromalacia
–Cartilage fibrillation
–Erosion

Exposure of subchondral bone plate
–Subchondral sclerosis (eburnation, ivory)
–Cyst formation
–Small fractures

•Osteophyte formation (lipping) outward growth of bone at the margins of articular surfaces;;
Formed by enchondral ossification
•Joint mice (detached fragments of bone)-> pain and recurrent locking
•Osteoporosis

Secondary changes •Thickening of the synovium with minimal inflammation
•Atrophy of the muscle
•Deformity of the joint
–Osteophyte formation
–Subluxation (partial dislocation)
•Osteoporosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Explain osteophyte formation in osteoarthritis

A
  • Heberden’s nodes are osteophytes producing palpable enlargement at the distal interphalangeal joints and often an early manifestation of osteoarthritis
  • Bouchard nodes are similar but on the proximal interphalangeal joints
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Clinical features of osteoporosis

A
•Asymptomatic
•Symptomatic
–Severe pain
–Morning stiffness
–Restricted movement
–Crepitous
–Compression of nerve root by osteophytes
–Deformity
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Investigations a/w osteoarthritis

A
•X-ray
•Negative serology (exclude RA) 
•Synovial fluid aspirate
–Synovial fluid is clear and viscous
–Cell count is slightly raised or normal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Tx for osteoarthritis

A

Glucosamine and chondroitin, s adenosylmethioninine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Define RA

A

Autoimmune systemic disorder that affects many organs especially (joints, skin, heart, lungs, eyes, lymph nodes and marrow)
•Affects 3% of women and 1% of men
•Most cases arise in young or middle-aged females
•Course unpredictable
–Insidious
–Remittent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

CRITERIA FOR RHEUMATOID ARTHRITIS

A
Four or more of the following
–Morning stiffness
–Arthritis of three or more joints
–Arthritis of the hands
–Symmetrical arthritis
–Rheumatoid nodule
–Serum rheumatoid factor
–Characteristic x-ray findings
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Pathogenesis for RA

A

Genetic susceptibility
•Associated with HLADR4
•30% concordance between monozygotic twins

Autoimmune reaction
•Type IV hypersensitivity (CD4+ T-cells)
•Autoantibodies ( B-cells)
•Cytokines (IL-1 and TNF)  injury

Microbial agent
•? Parvovirus, mycobacteria, mycoplasma
•? EBV
–EBV detected in synovium
–EBV and type II collagen share similar epitopes
–B cell infected by EBV  RF
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Describe rf

A

•80% patients with rheumatoid arthritis
•IgM antibody against the FC portion of the IgG
•Titre correlates with severity of disease
•RF-IgG immune complexes
–Synovial fluid and synovial membrane
–Circulating immune complexes-> extra-articular manifestations
•Present in < 5% of normal elderly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Morphology of RA

A

Classically affects the SYNOVIUM of small joints of hands especially
– Proximal interphalangeal joints (swan-neck deformity, boutonniere deformity, ulnar deviation of fingers)
–Metacarophalangeal (radial deviation of wrist)
•Symmetrical
•Polyarticular

Secondary changes

  • affects joints
  • osteoarthritis
  • osteoporosis
  • muscle wasting
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Pathological features of RA

A

•Synovial hyperplasia
•Lymphocytes and plasma cells with lymphoid follicle formation and occasional polymorphs in synovium
•Fibrin
•Pannus formation (from Latin: a cloth)
–Organised inflammatory tissue within the synovium which can erode the articular cartilage
•Subchondral cyst formation
•Juxta-articular erosion at the joint margin
•Fibrous ankylosis

22
Q

List some common extra articular manifestations

A
•Rheumatoid lung
–Pulmonary fibrosis
–Pulmonary nodules
•Uveitis and scleritis
•Vasculitis
•Amyloidosis
•Subcutaneous nodule
•Lymphadenopathy
•Sjogren’s Syndrome (xerostomia, keratoconjunctivitis )
23
Q

What is a common syndrome a/w long standing RA?

A

Felty’s syndrome

splenomegaly
severe leucopenia and anemia

24
Q

Lab investigations for RA

A

Bloods - assess normocytic anemia, ESR

serology- RF and other autoantibodies ;; anti DNA antibodies

25
Q

Treatment of RA

A

•Non steroidal anti-inflammatory drugs
•Steroids
•Gold
•Antimetabolites- azathioprine, methotrexate, cyclosoprine
•Surgery- subluxation of the cervical spine
•New drugs
–Antibodies against TNF
–Omega 3 (blocks production of leukotriene B4 and interlukin 1)

26
Q

Define seronegative spondylitis

A
•A group of diseases with negative RF
•Involvement of the sacroiliac joint and spine (sarcoilitis and spondylitis)
• HLA-B27
–Ankylosing spondylitis
–Reactive arthritis
•Reiter syndrome
-Enteropathic arthritis
–Psoriatic arthritis
27
Q

Define ankylosing spondylitis

A

aka bambo spine
•Chronic inflammatory disorder of lumbar spinal and sacroiliac joints
•HLA B27 (90%)
•Young males
•Autoantibodies directed at joint elements after infection
•Peripheral arthritis (30%), uveitis, aortic incompetence and amyloidosis

28
Q

Define Reiter’s syndrome

A
•Affects young males
•HLA-B27 (80%)
•Autoimmune reaction following
–genitourinary infection (Chlamydia)
–gastrointestinal infection (Salmonella, Shigella,
Yersinia, Campylobacter)
•Defined by a triad of
–Arthritis affecting knees, ankles and spine
–Urethritis/cervicitis
–Conjunctivitis
29
Q

Define infective arthritis

A
•Haematogenous spread (most common)
•Spread from adjacent infective foci
•Direct inoculation
–Local trauma
–Insertion of surgical prosthesis
30
Q

Causes of suppurative arthritis

A
•Staphylococcus aureus
–Most common cause in the very young and old
–Most destructive
•Haemophilus influenzae
–In young children <2 years
•Gonococcus
–In healthy young sexually active individuals
•Streptococci
•E.coli
•Pseudomomas
•Salmonella
– Sickle cell disease
31
Q

Features of suppurative arthritis

A
•Acutely painful
•Swollen joints
•Fever
•Decreased range of motion
•↑ WCC
change in joint fluid
32
Q

Features of synovial fluid in infectious arthritis

A
•Aspiration of joint effusion under sterile conditions
–Colour-yellow / green
–Clarity- purulent
– WBC > 50,000
–PMNs >75%
–Glucose less than blood
–Gram stain usually positive
–Culture often positive
33
Q

Describe tuberculous arthritis

A
  • Spread from adjacent tuberculous osteomyelitis or haematogenous spread
  • Spine most commonly affected, hip next
  • Cross cartilage barriers unlike bacterial infections
  • Destructive arthritis ankylosis and deformity
  • Typical granulomatous inflammation
34
Q

Define lyme’s arthritis

A

•Transmitted by a tick bite
•The pathogenic organism is Borrelia burgdorferi (Spirochete)
Appears in stage 3 (late chronic form) - destructive arthritis ; migratory arthritis affecting large joints. Can occur w neuropathy at this stage

35
Q

Define gout arthritis

A
  • Males > females
  • Peak incidence in the fifth decades
  • 25% of cases are familial
  • Disorder of purine metabolism-> hyperuricaemia
  • Serum urate level above 7 mg/dl
  • Hyperuricaemia-primary or secondary
36
Q

Risk factors / Causes for primary gout

A
90%
•Age (rare before 30)
•Family history
•Alcohol consumption
•Obesity
37
Q

Causes for sec gout

A

10%
–Overproduction of uric acid usually associated with an excessive breakdown of nucleic acids (leukaemia, multiple myeloma, massive cell lysis produced by cytotoxic drug therapy
–Renal undersecretion (e.g., renal failure, diuretic drugs, salicylate and ethanol)
–Enzyme deficiency: Hypoxanthine guanin phosphorybosyl transferase (HGPRT)

38
Q

Pathogenesis of gout arthritis

A

•Deposition of urate crystals on the surface of the articular cartilage
•Interaction with leucocytes->degenerative changes
•Mono-articular
–Metatarsophalangeal joint of big toe is the most commonly affected joint
•Deposition of uric acid in tissue results in tophus formation

39
Q

Outline stages of gout

A
  • Acute inflammatory arthritis
  • Asymptomatic periods between attacks
  • Chronic deposition of urate in and around joints (tophi)
40
Q

Outline complications of gout

A

Renal failure
Renal calculi
Interstitial nephritis

41
Q

Dx of gout?

A

Pathological

joint fluid aspirate- needle shaped crystals and neutrophils –Alcohol fixation (crystals are water soluble, dissolve during formalin processing)

synovial (membrane) biopsy

42
Q

Define pseudogout

A
  • Deposition of calcium pyrophosphate on articular cartilage (usually knees)
  • Males = females
  • Age incidence: usually over 50 years of age

Classified into
–Primary (idiopathic)
–Hereditary
–Secondary (hyperparathyroidism, hypothyroidsm, haemochromatosis and diabetes mellitus)

43
Q

Features of pseudogout

A
  • Asymptomatic until the crystals are shed into the joint space (spontaneous or due to trauma)
  • Synovial fluid contains neutrophils and rhomboid crystals
  • Knees, wrists and shoulders
44
Q

Define hypertrophic osteoarthropathy

A

•Characterised by:
–New bone formation at the distal end of long bones, in metacarpal and metatarsal bones, and in proximal phalanges
–Arthritis of the adjacent joint
–Clubbing of digits
•Patients usually have an underlying disease, most commonly bronchogenic carcinoma
•Rarely it occurs as an idiopathic disorder which is occasionally familial

45
Q

Outline tumours of soft tissue

A
tumors of mesenchymal origin
benign 
malignant =sarcoma–Rare
–Males > females
–Occurs in organs and soft tissues
46
Q

Risk factors for soft tissue sarcomas

A
Risk factors
–Radiation
–Chemical agent (e.g., venyl chloride and angiosarcoma)
–Viruses e.g., Kaposi sarcoma
–Genetic syndromes (Li Fraumeni)
47
Q

Classify of soft tissue tumours

A
•Tumours of adipose tissue
–Lipoma
–Liposarcoma
•Tumours of smooth muscle
–Leiomyoma
–Leiomyosarcoma
•Tumour of skeletal muscle
–Rhabdomyoma
–Rhabdomyosarcoma
•Fibrohistiocytic tumours
–Fibrous histiocytoma
–Malignant fibrous histiocytoma
•Vascular tumours
–Haemangioma
–Angiosarcoma
•Peripheral nerve tumours
–Neurofibroma
–Malignant peripheral nerve sheath tumours
•Tumours of uncertain histogenesis
–Synovial sarcoma
48
Q

Prognosis of soft tissue sarcomas depends on..?

A

1.Histologic type
2.Tumour grade
–Degree of differentiation of the tumor
–Cellularity of the tumor
–Pleomorphism of the tumor cells
–The presence and number of mitoses
–The presence of necrosis
3.Stage of the tumour
4.Location (superficial- better prognosis)

49
Q

Diagnosis of soft tissue sarcomas

A
•Histologic examination
•Immunohistochemistry
–Nearly all vimentin positive
–Leimyosaroma (desmin and actin positive)
–Rhabdomyosarcoma (Myoglobin positive)
•Molecular diagnosis
–Some have specific genetic abnormality
•Ewing’s sarcoma t(11;22)
•Synovial Sarcoma t(X;18)
50
Q

Define psoriatic arthritis

A

affects 5% of people w psoriasis
Arthritis affecting DIP, ankles, knees and spine
HLA B27
Spontaneous remission

51
Q

Define enteropathic arthritis

A

chronic inflam bowel diseases (UC and chron’s)

following bowel infection
salmonella
shigella
yersinia
campylobacter