Calcium Pyrophosphate Arthritis
(Calcium Pyrophosphate Dihydrate Crystal Deposition Disease; Acute Calcium Pyrophosphate Arthritis; Chondrocalcinosis; Pyrophosphate Arthropathy; Pseudogout)
(See also Overview of Crystal-Induced Arthritides.)
CPPD crystal deposition (chondrocalcinosis, pyrophosphate arthropathy), whether symptomatic and asymptomatic, becomes more common with age.
Asymptomatic chondrocalcinosis is common in the knee, metacarpophalangeal joints, hip, wrist, annulus fibrosus of the intervertebral disks, symphysis pubis, and spine. Men and women are affected about equally.
The cause of calcium pyrophosphate arthritis is unknown. Frequent association with other conditions, such as trauma (including surgery), hypomagnesemia, hyperparathyroidism, gout, hemochromatosis, and old age, suggests that calcium pyrophosphate dihydrate (CPPD) crystal deposits are secondary to degenerative or metabolic changes in the affected tissues.
Some cases are familial, usually transmitted in an autosomal dominant pattern, with complete penetration by age 40.
Recent studies indicate that the ANK protein is a central factor in producing excess extracellular pyrophosphate, which promotes CPPD crystal formation. ANK protein is a putative transporter of intracellular pyrophosphate to the extracellular location where CPPD crystals form.
Acute, subacute, or chronic arthritis can occur, usually in the knee or other large peripheral joints; thus, calcium pyrophosphate crystal disease can mimic many other forms of arthritis. Acute attacks are sometimes similar to gout but are usually less severe. There may be no symptoms of calcium pyrophosphate arthritis between attacks or continuous low-grade symptoms in multiple joints, similar to RA or osteoarthritis. These patterns tend to persist for life.
Calcium pyrophosphate arthritis should be suspected in older patients with arthritis, particularly inflammatory arthritis.
Diagnosis of calcium pyrophosphate arthritis is established by identifying rhomboid- or rod-shaped crystals in synovial fluid that are not birefringent or are weakly positively birefringent on polarized light microscopy. Joint fluid in acute attacks has findings typical of inflammation; thus, coincident infectious arthritis and gout (other common causes of inflammatory joint fluid) must also be excluded. Infectious arthritis is ruled out based on Gram stain and culture findings. Gout is usually best ruled out by the absence of urate crystals in fluid from the inflamed joint. X-rays or ultrasonography are indicated if synovial fluid cannot be obtained for analysis; findings of multiple linear or punctate calcification in articular cartilage, especially fibrocartilages, support the diagnosis but do not exclude gout or infection. Typical ultrasonographic findings of gout (double contour sign) may simulate findings of calcium pyrophosphate crystal deposits.
The prognosis for individual attacks of acute calcium pyrophosphate arthritis is usually excellent. However, chronic arthritis can occur, and severe destructive arthropathy resembling neurogenic arthropathy (Charcot joints) occasionally occurs.
Symptoms of acute synovial effusion abate with synovial fluid drainage and instillation of a microcrystalline corticosteroid ester suspension into the joint space (eg, 40 mg prednisolone acetate or prednisolone tertiary butylacetate into a knee).
Asymptomatic chondrocalcinosis becomes common with age, particularly in the knee, hip, wrist, annulus fibrosus of the intervertebral disks, and symphysis pubis.
Arthritis can affect the knee and large peripheral joints and mimic other forms of arthritis.
Examine joint fluid for characteristic rhomboid- or rod-shaped crystals in synovial fluid that are not birefringent or are weakly positively birefringent, and exclude joint infection.
For acute symptoms, treat with an intra-articular corticosteroid or an oral NSAID.
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