2016, Number 3
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An Med Asoc Med Hosp ABC 2016; 61 (3)
Calcium pyrophosphate deposition disease: 60 Mexican patients
Canoso JJ
Language: Spanish
References: 22
Page: 188-194
PDF size: 267.62 Kb.
ABSTRACT
Objective: There are no previous Mexican reports of calcium pyrophosphate deposition disease.
Material and methods: The clinical records of 7,200 patients seen by the author between 1995 and 2015 were reviewed. Cases of calcium pyrophosphate deposition disease were identified by means of a «Windows search» using the appropriate search terms. Patients were classified clinically, by the results of X-ray studies, and according to the findings in the synovial fluid analysis.
Results: There were 60 patients with calcium pyrophosphate deposition disease, 39 female (median age 76), and 21 male (median age 71). Twenty-two patients had acute arthritis (pseudogout), 20 had calcium pyrophosphate deposition disease plus osteoarthritis (OA), 16 had chronic arthritis, and two had calcium pyrophosphate crystals in incidental effusions. Three patients had a destructive arthropathy. Despite the female predominance, acute arthritis occurred equally in both sexes. Chondrocalcinosis was present in 59 patients. Forty patients had a joint aspiration, and in 37 of them, calcium pyrophosphate crystals were found in synovial fluid. Of these, in three, urate crystals were concurrently seen. Rheumatoid arthritis had been erroneously diagnosed in five of the patients.
Conclusions: Calcium pyrophosphate deposition disease occurs in Mexico and may predominate in European ascent individuals. When calcium pyrophosphate crystals are identified in acute arthritis and in exacerbations of osteoarthritis, a favorable course may be predicted as these episodes respond well to low-dose oral steroids or a depo-steroid injection. Long-term prophylaxis with colchicine may prevent recurrences of pseudogout and decrease pain in chronic calcium pyrophosphate deposition disease.
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