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Which investigations should be performed to confirm a diagnosis of calcium pyrophosphate deposition disease (CPPD) in a suspected case?
Answer
To confirm a diagnosis of calcium pyrophosphate deposition disease (CPPD) in a suspected case, the definitive investigation involves the identification of calcium pyrophosphate crystals [1, (Tsui, 2012)]. This is typically achieved through the microscopic examination of synovial fluid obtained from an affected joint 1. The identification of specific crystals in synovial fluid is a cornerstone for definitively diagnosing crystal arthropathies, similar to how urate crystals confirm gout 1,2. The presence of these crystals is fundamental to understanding the mechanisms of crystal deposition in CPPD and is a key aspect in its nomenclature and classification [1, (Tsui, 2012), (Tedeschi, 2019)].
Key References
- NG219 - Gout: diagnosis and management
- CKS - Gout
- CKS - Axial spondyloarthritis (including ankylosing spondylitis)
- NG33 - Tuberculosis
- CKS - Olecranon bursitis
- NG100 - Rheumatoid arthritis in adults: management
- (Tsui, 2012): Genetics and mechanisms of crystal deposition in calcium pyrophosphate deposition disease.
- (Tedeschi, 2019): Issues in CPPD Nomenclature and Classification.
- (Cadiou et al., 2022): Calcium pyrophosphate deposition (CPPD) in a liver transplant patient: are hypomagnesemia, tacrolimus or both guilty? A case-based literature review.
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