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Idiopathic Calcium Pyrophosphate Dihydrate (CPPD) Crystal Deposition Disease in a Young Male Patient: A Case Report
Journal of Korean Medical Science ; : 917-920, 2003.
Article in English | WPRIM | ID: wpr-28609
ABSTRACT
Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease is a disease of the elderly and extremely rare in young individuals. If young people develop CPPD crystal deposition disease, it may be associated with metabolic diseases such as hemochromatosis, hyperparathyroidism, hypophosphatasia, hypomagnesemia, Wilson's disease, hypothyroidism, gout, acromegaly, and X-linked hypophosphatemic rickets. Therefore, in young-onset polyarticular CPPD crystal deposition disease, investigation for predisposing metabolic conditions is warranted. We report a case of a young male patient with idiopathic CPPD crystal deposition disease, who did not have any evidences of metabolic diseases after thorough evaluations. As far as we know, this is the first report of a young male patient presented with idiopathic CPPD crystal deposition disease.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Shoulder Joint / Calcium Pyrophosphate / Cartilage, Articular / Diagnosis, Differential / Knee Joint / Metabolic Diseases Type of study: Diagnostic study Limits: Adult / Humans / Male Language: English Journal: Journal of Korean Medical Science Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Shoulder Joint / Calcium Pyrophosphate / Cartilage, Articular / Diagnosis, Differential / Knee Joint / Metabolic Diseases Type of study: Diagnostic study Limits: Adult / Humans / Male Language: English Journal: Journal of Korean Medical Science Year: 2003 Type: Article