CPPD Flashcards

1
Q
  • deposition of CPP crystals in articular tissues is most common in the elderly
  • occurs in 10-15% of persons age 65-75 years , 30-50% of those >85 years
  • Asymptomatic in most cases
  • cause is uncertain
A

CALCIUM PYROPHOSPHATE DEPOSITION (CPPD) DISEASE

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2
Q

Mutations in the ANKH gene

A

CPPD

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3
Q

CLINICAL MANIFESTATIONS OF CPPD

A
  • may be asymptomatic
  • acute/subacute or chronic
  • may cause acute synovitis superimposed on chronically involved joints
  • association with or enhancement of peculiar forms of osteoarthritis
  • induction of severe destructive disease that may radiographically mimic neuropathic arthritis
  • intervertebral disk and ligament calcification with restriction of spine mobility, the crowned
    dens syndrome, or spinal stenosis (most commonly seen in the elderly)
  • production of chronic symmetric synovitis that is clinically similar to rheumatoid arthritis
  • rarely periarticular tophus-like nodules
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4
Q

Most frequently affected in CPPD

A

Knee joint

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5
Q

Other sites affected in CPPD

A
  • wrist
  • shoulder
  • ankle
  • elbow
  • hands
  • temporomandibular joint
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6
Q

Is seen in at least 2/3 of patients

A

polyarticular

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7
Q

diagnostic likelihood of CPPD

A

If radiographs or ultrasound reveal punctate and/or linear radiodense deposits within fibrocartilaginous joint menisci or articular hyaline cartilage (chondrocalcinosis)

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8
Q

Definitive diagnosis of CPPD

A

typical rhomboid or rodlike crystals (generally weakly positively birefringent or
nonbirefringent w/ polarized light) in synovial fluid or articular tissue

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9
Q

is essential to rule out the possibility of infection in dx of CPPD

A

synovial fluid analysis with microbial cultures

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10
Q

synovial fluid analysis with microbial cultures IN CPPD

A

Neutrophil

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11
Q

TX of CPPD

A
  • rest, joint aspiration, and NSAIDs or by intraarticular
    glucocorticoid injection may result in more rapid return to prior status.
  • Low doses of colchicine for frequent recurrent attacks
  • Severe polyarticular attacks usually require short courses of glucocorticoids or an IL-18 antagonist, anakinra
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12
Q

is the primary mineral of normal bone and teeth

A

Apatite

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13
Q

Apatite crystals are deposited primarily on

A

matrix vessels

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14
Q

Apatite aggregates are commonly present in synovial fluid in an extremely destructive chronic arthropathy of the elderly that occurs most often in the ___

A

shoulders (Milwaukee shoulder)

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15
Q

most common sites of apatite deposition include

A
  • bursae and tendons in and/or around the knees,
  • shoulders,
  • hips, and
  • fingers
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16
Q

Clinical manifestations of CALCIUM APATITE DEPOSITION DISEASE

A
  • asymptomatic radiographic abnormalities,
  • acute synovitis,
  • bursitis,
  • tendinitis,
  • chronic destructive arthropathy
17
Q

synovial fluid leukocyte count in apatite arthritis is ___ despite dramatic symptoms, with predominance of mononuclear cells

A

usually low (<2000/uL)

18
Q

Clumps of crystals may appear as 1- to 20-um shiny intra- or extracellular
nonbirefringent globules or aggregates that stain purplish with _____
and bright red with ____.
Tetracycline binding and other investigative techniques are under
consideration as labeling alternatives.

A
  • Wright’s stain
  • alizarin red S
19
Q

is a rare hereditary metabolic disorder

A

Primary oxalosis

20
Q
  • Hyperoxalemia
  • deposition of CaOx crystals in tissues
  • nephrocalcinosis and renal failure
  • Acute and/or chronic CaOx arthritis, periarthritis, and bone disease may complicate primary oxalosis during later years of illness
A

CaOx DEPOSITION DISEASE

21
Q
  • more common than the primary disorder
  • In chronic renal disease, CaOx deposits have long been recognized in visceral
    organs, blood vessels, bones, and cartilage and are now known to be one of the causes of arthritis in chronic renal failure
A

Secondary oxalosis

22
Q

CaOx-induced synovial effusions are usually ____ with ___

A

noninflammatory, with <2000 leukocytes/uL, or mildly inflammatory

23
Q

most easily recognized forms of CaQOx crystals are ____, have strong birefringence and stain with alizarin red S

A

bipyramidal

24
Q

TREATMENT: CaOx DEPOSITION DISEASE

A
  • NSAIDs,
  • colchicine,
  • intraarticular glucocorticoids,
  • and/or an increased frequency of dialysis has produced only slight
    improvement.