Joint Pathology Flashcards

1
Q

Normal Joint

Architecture

A

Components of Cartilage:

  • Chondrocytes
  • Water
  • Collagen
  • Proteoglycans
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2
Q

Osteoarthritis

Overview

A

“Degenerative Joint Disease”

  • See deterioration and loss of articular cartilage
  • Takes place over the course of many years
  • Affects weight bearing joints
  • Pathogenesis: biomechanical and biochemical theories
  • Clinical course: insidious with progressive pain and disability
    • No constitutional signs, differential from RA
    • No specific preventative or maintenance therapy (as of now)
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3
Q

Osteoarthritis

Morphology

A
  • Loss of cartilage
  • Exposure and eburnation of subchondral bone
  • ± Subchondral cyst formation
  • Osteophytes aka “Joint mice”
  • Heberden’s nodes
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4
Q

Osteoarthritis

Symptoms

A
  • Joint pain associated with movement
  • Limitation of motion
  • Stiffness after periods of rest
  • Referred pain
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5
Q

Osteoarthritis

Clinical Manifestations

A
  • Changes in shape of the joint
  • Malalignment
  • Limitation of motion
  • Instability
  • Spasm or atrophy of surrounding muscles
  • Fine crepitation on joint motion
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6
Q

Rheumatoid Arthritis (RA)

Overview

A

Systemic, relapsing, chronic destructive synovitis

  • Etiology unknown, course unpredictable
  • Women affected 3x more than men
  • Diagnosis by physical exam and lab studies
  • Shortened life expectancy, often due to complications of therapy
  • Variants: juvenile RA, Felty’s syndrome, ankylosing spondylitis
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7
Q

Rheumatoid Arthritis (RA)

Morphology

A
  • Irregular, hypertrophied synovial membrane
    • ‘Villiform’ structure
    • Lymphoid inflammation
      • Can contain lymphoid follicles
  • Chronic inflammation
  • Pannus formation (scarring @ edges of joint space)
  • Fibrous and bony ankylosis (bone fusion)
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8
Q

Felty’s Syndrome

A

Constellation of sx:

  • Rheumatoid arthritis
  • Splenomegaly
  • Neutropenia
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9
Q

Rheumatoid Arthritis (RA)

Pathogenesis

A

Believed to be autoimmune disease.

(Theory that process can be initiated by a virus)

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10
Q

Rheumatoid Arthritis (RA)

Course

A

Disease can follow various courses:

  • Single episode followed by sustained remission
  • Initial episode followed by complete remissions and exacerbations
  • Acute illness with intercurrent milder disease activity
  • Sustained disease activity
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11
Q

Rheumatoid Arthritis (RA)

Intra-articular Manifestation

A
  • Joints inflamed
  • Progressive stiffness and ankylosis (fusion of the bones)
  • Hand becomes claw-like with ulnar deviation
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12
Q

Rheumatoid Arthritis (RA)

Extra-articular Manifestations

A
  • Subcutaneous and subperiosteal nodules
    • Fibrin core surrounded by palisading histiocytes
  • Constitutional sx (malaise, fatigue, diffuse pain, fever)
  • Organs and Tissue involvement:
    • Pulmonary
    • Cardiac
    • Ocular
    • Neurological
    • Vascular
  • RA pts often have Sjogren’s syndrome
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13
Q

Rheumatoid Arthritis (RA)

Pulmonary Involvement

A
  • Pleuritis
  • Pleural effusion
  • Pulmonary fibrosis
  • Parenchymal rheumatoid nodules
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14
Q

Caplan’s Syndrome

A

Peumoconiosis and rheumatoid arthritis

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15
Q

Rheumatoid Arthritis (RA)

Vascular Involvement

A
  • Digital Arteritis
    • Focal ischemic areas with pitting
    • Digital gangrene
  • Raynaud’s phenomenon
  • Leg ulcers
  • Necrotizing systemic vasculitis
    • Mesenteric
    • Renal
    • Coronary
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16
Q

Suppurative (Septic) Arthritis

A
  • Destructive non-specific acute inflammatory reaction
  • Hematogenous or direct spread to single large joints
  • See Gonococci, Staph, Strep, Gram negative bacilli
17
Q

Tuberculous Arthritis

A
  • Caseating granulomas similar to those seen in TB elsewhere
  • Causes ankylosis, skin sinuses, or damage to spinal cord
  • Insidious chronic disease in children
  • Affects the spine, hip, etc
  • Early diagnosis essential
18
Q

Lyme Disease

A
  • Spirochetal infection
  • Transmitted by deer ticks
  • Progression:
    • First stage: skin lesion
    • Second stage: cardiac and nervous systems affected
    • Third stage: chronic disabling arthritis in 10% of cases
  • Serologic diagnosis
  • Abx therapy essential
19
Q

Gout

Overview

A
  • Hyperuricemia
  • Recurrent acute arthritis following asymptomatic intervals
  • Deposition of tophi
  • Renal impairment may occur
  • Few with hyperuricemia develop gout
  • Asymptomatic hyperuricemia does not require treatment
  • 95% of cases in adult males, usually in great toe
20
Q

Gout

Pathogenesis

A

Pathogenesis relates to production and excretion of uric acid:

  • Primary Gout
    • Due to overproduction of uric acid
    • Cause of overproduction generally unknown
  • Secondary Gout
    • Can be due to reduced excretion
      • Glomerular or tubular defect or due to certain drugs
      • Lead poisoning of the kidneys in Victorian England
    • Can be due to increased production
      • Chemotherapy
21
Q

Gout

Morphology

A
  • Acute arthritis due to precipitation of urates in joint fluid
    • Birefringent crystals phagocytized by neutrophils and MΦ ⇒ release of harmful products
    • Attack ends when crystals go back into solution
  • Chronic arthritis is due to progressive precipitation of urates into synovium ⇒ destruction and ankylosis of joint
  • Tophus: inflammatory mass of urates, pathognomonic
  • Renal involvement by gout can include stones or urate deposits
22
Q

Gout

Clinical Phases

A
  1. Asymptomatic hyperuricemia
  2. Recurrent acute gouty arthritis
  3. Chronic gouty arthritis

Diagnosis important because treatment is available

23
Q

Pseudogout

A

“Calcium pyrophosphate crystal deposition disease”

  • Get precipitation of crystals in menisci and intervertebral discs
  • Deposits can enlarge and rupture into the joint
  • Produces inflammation
  • Often asymptomatic
24
Q

Seronegative Spondyloarthropathies

A
  • Ankylosing spondylitis
  • Reactive arthritis
  • Enteropathic arthritis
  • Psoriatic arthritis
25
Q

Ankylosing Spondylitis

A

“Bechterew disease”

  • Rare type of arthritis that causes pain and stiffness in the spine
    • Most often affects sacroiliac joints
  • Lifelong condition
  • Seen in adolescent males
  • 90% have HLA B-27
26
Q

Reactive Arthritis

A

“Reiter syndrome”

  • Triad of:
    • Arthritis
    • Non-gonococcal urethritis or cervicitis
    • Conjunctivitis
  • 80% are HLA B-27
  • Autoimmune reaction to GI or GU infection
27
Q

Enteropathic Arthritis

A
  • Induced by GI infection with Yersinia, Salmonella, Shigella, Campylobacter
  • Often HLA B-27
28
Q

Psoriatic Arthritis

A
  • Form of arthritis that affects some pts with psoriasis
  • Type of inflammatory arthritis
  • Affects DIP joints of hands and feet and large joints
  • Symptoms include joint pain, stiffness, and swelling
  • Tx includes antiinflammatories, steroid injections, or joint replacement surgery
29
Q

Ganglion Cyst

A

Fluid-filled sac arising from an adjacent joint capsule or tendon sheath

Most common mass that develops in the hand

30
Q

Nodular Tenosynovitis

A
  • Common
  • More frequent in women
  • Usually seen on hands and feet, more often proximally and on flexor surfaces
  • May erode contiguous bone by pressure
  • Pathogenesis: Controversial, some view as reactive, others see it as neoplastic (but usually benign)
  • Gross appearance:
    • Single mass, usually 1–3cm diameter
    • Fairly well-defined capsule
    • May be somewhat lobulated
    • Varies in color from whitish gray to yellowish brown
  • Microscopic: dense, cellular tissue