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Updated: Jan 22, 2026

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Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
Published on: April 9, 2014
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Osteopoikilosis: case series from Portuguese Rheumatology Centers
Nathalie Madeira1, Sara Ganhão2, Raquel Miriam Ferreira2
1Instituto Português de Reumatologia.
Acta Reumatologica Portuguesa
|June 29, 2019
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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