Calcium Pyrophosphate Deposition (CPPD) disease, also known as pseudogout, is a condition caused by the accumulation of calcium pyrophosphate (CPP) crystals in the joints. These crystals lead to inflammation and are composed of calcium and pyrophosphate. CPPD is a common type of inflammatory joint disease, second only to gout. Some people with CPPD may not experience any symptoms, while others might suffer from sudden acute joint inflammation, and some may develop chronic joint inflammation.
The symptoms of CPPD can vary greatly and can affect multiple joints, often resembling other joint diseases. Symptoms include:
Risk factors for CPPD mainly include older age, joint injury history, genetics, conditions like hyperparathyroidism and hemochromatosis, and low magnesium levels.
Diagnosing CPPD involves a combination of patient history, physical examination, joint fluid analysis, and imaging like X-rays or ultrasounds. Identifying CPP crystals in joint fluid is key and is done using microscopy. This analysis not only confirms CPPD but also helps exclude conditions like gout or infectious arthritis. Radiographic evidence of crystal deposits in cartilage, known as chondrocalcinosis, is also indicative. Ultrasound can be more sensitive than X-rays in detecting chondrocalcinosis and can guide joint aspiration in difficult-to-access joints.
Current treatments for CPPD focus on managing symptoms, as there is no cure to remove CPP crystals from cartilage. Treatments include:
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