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Scrotal calcinosis: a very rare multiple clinical presentation
Clinical and Experimental Dermatology, 10/16/09

Figus A et al. – The authors report a very rare case of an SC in a 59–year–old white man who presented with multiple nodules with different clinical patterns in the scrotum, which had been present for > 42 years. Despite the rarity and the multiple long–lasting lesions, surgical excision of the scrotal nodules can offer a very good aesthetic outcome in a single procedure even under local anaesthesia.

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Tumoral calcinosis in children, a challenging and possibly underdiagnosed condition
Acta Orthopaedica Belgica, 11/17/09 Relevance Score: 88%

Tumoral Calcinosis Mimicking Recurrent Osteosarcoma
Radiology Case Reports, 10/23/09 Relevance Score: 87%

Familial tumoral calcinosis and hyperostosis–hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3
Skeletal Radiology, 10/21/09 Relevance Score: 84%

Familial Tumoral Calcinosis: From Characterization of a Rare Phenotype to the Pathogenesis of Ectopic Calcification
Journal of Investigative Dermatology, 10/30/09 Relevance Score: 83%

Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
Arthritis Research & Therapy, 10/27/09 Relevance Score: 83%