Literature DB >> 14676457

Idiopathic calcium pyrophosphate dihydrate (CPPD) crystal deposition disease in a young male patient: a case report.

Joong Kyung Ahn1, Hyung Jin Kim, Eung Ho Kim, Chan Hong Jeon, Hoon-Suk Cha, Chul Won Ha, Joong Mo Ahn, Eun-Mi Koh.   

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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Year:  2003        PMID: 14676457      PMCID: PMC3055143          DOI: 10.3346/jkms.2003.18.6.917

Source DB:  PubMed          Journal:  J Korean Med Sci        ISSN: 1011-8934            Impact factor:   2.153


  1 in total

1.  Calcium Pyrophosphate Dihydrate Deposition Disease in Young Patients: Two Case Reports.

Authors:  Geetha Wickrematilake Wickrematilake
Journal:  Arch Rheumatol       Date:  2016-12-08       Impact factor: 1.472

  1 in total

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