Article
ARP Rheumatology
Osteopoikilosis: case series from Portuguese Rheumatology Centers
Abstract
Osteopoikilosis (OPK) is a rare, hereditary, usually asymptomatic disease characterized by the presence of multiple, well-defined sclerotic lesions distributed in peri-articular locations, frequently diagnosed as an incidental finding. Differential diagnosis with osteoblastic metastases is fundamental. This article reports six cases of OPK diagnosed in Portuguese Rheumatology Centers.
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Publication:
2019-03-15
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Nathalie Madeira, Sara Ganhão, Raquel Ferreira, Ana Duarte, Raquel Freitas, Luís Miranda. Osteopoikilosis: case series from Portuguese Rheumatology Centers. ARP, Vol 44, nº1 2019:78-83. PMID: 31249279
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