Calcinosis Cutis Universalis in a Patient with Systemic Sclerosis

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Idiopathic calcinosis cutis universalis

Case A 12-years old girl with complaints of multiple lumps on her body since 1 years prior to admission. Two years prior to admission patient complained of movement limitation due to pain when doing leg lifting, squatting and standing up. One years prior to admission patient got bilateral symmetrical lumps on hip, corn size and getting bigger. Two months prior to admission the lumps got rupture...

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[Calcinosis cutis in a patient with systemic lupus erythematosus].

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Unusual Idiopathic Calcinosis Cutis Universalis in a Child

Calcinosis cutis is an uncommon disorder characterized by the progressive deposition of crystals of calcium phosphate (hydroxyapatite) in the skin in various areas of the body. It is classified into four types according to etiology, namely as dystrophic if calcium and phosphorus levels are normal and tissue damage is present, as idiopathic if calcium and phosphorus levels are normal and no tiss...

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Calcinosis cutis universalis associated with systemic lupus erythematosus: an exuberant case.

Calcinosis cutis is an uncommon disease of unclear pathophysiology that is often disabling. It is characterized by the formation of calcium deposits in the skin or subcutaneous tissue. It is classified into four subtypes: dystrophic, metastatic, idiopathic or iatrogenic. It may be seen in a variety of systemic diseases such as hyperparathyroidism and hypervitaminosis D, but is most commonly fou...

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Calcinosis cutis in a pediatric patient with Burkitt's lymphoma.

Calcinosis cutis, an uncommon disorder characterized by hydroxyapatite crystals of calcium phosphate deposited in the skin, has been described infrequently in childhood. Cutaneous calcification may be divided into four major categories: dystrophic, metastatic, idiopathic, and iatrogenic. Here, we report an example of iatrogenic type with a 4-year-old boy who diagnosed with Burkitt's lymphoma, a...

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ژورنال

عنوان ژورنال: Turkiye Klinikleri Journal of Case Reports

سال: 2020

ISSN: 2147-9291

DOI: 10.5336/caserep.2019-65627