Results 11 to 20 of about 22,901 (252)
Avid 18F-FDG Uptake in Idiopathic Tumoral Calcinosis Mimicking Lymph Node Metastasis [PDF]
Diagnostics, 2017 Tumoral calcinosis is a benign condition characterized by periarticular calcified lesions that is frequently observed in patients with chronic renal failure. Tumoral calcinosis often presents with subcutaneous masses and joint swelling. We present a case
Jesper Strandberg, Helle D. Zacho
doaj +4 more sources
Unusual Idiopathic Calcinosis Cutis Universalis in a Child [PDF]
Case Reports in Dermatology, 2009 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.
Derya Alabaz +3 more
doaj +4 more sources
Calcinosis in Scleroderma [PDF]
Proceedings of the Royal Society of Medicine, 1976 J N Rosenberg, Jayne Lewis
openalex +4 more sources
Pharmacokinetics and Safety of Oral Pyrophosphate in Systemic Sclerosis Patients-A Pilot Study. [PDF]
ACR Open RheumatolObjective Calcinosis is a manifestation of systemic sclerosis with a severe negative impact on quality of life. Efforts to find a treatment for calcinosis have been hindered by our limited understanding of the underlying pathomechanism. We propose that extracellular pyrophosphate deficiency may have a causal role in the formation of these mineralized ...
Bodor G +5 more
europepmc +2 more sources
Journal of Inherited Metabolic Disease, 2010 Contains fulltext : 87587.pdf (Publisher’s version ) (Closed access)
Janssen, M.C.H., Sevaux, R.G.L. de
openaire +3 more sources
Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies [PDF]
, 2018 Hyperphosphatemic familial tumoral calcinosis (HFTC)/hyperostosis-hyperphosphatemia syndrome (HHS) is an autosomal recessive disorder of ectopic calcification due to deficiency of or resistance to intact fibroblast growth factor 23 (iFGF23). Inactivating
Burbelo +14 more
core +1 more source
Revista de Osteoporosis y Metabolismo Mineral, 2023 Resumen Caso clínico: presentamos el caso de una mujer de 48 años con dolor en senos maxilares y zonas temporales, en la que se apreciaron placas cálcicas subcutáneas faciales al realizar una tomografía axial computarizada (TC). La exploración física y los datos del laboratorio fueron normales.
Haro Herrera, Marina +2 more
openaire +3 more sources
Clinical phenotypes and biologic treatment use in juvenile dermatomyositis-associated calcinosis [PDF]
, 2018 Background Few risk factors have been identified for the development of calcinosis among patients with Juvenile Dermatomyositis, and currently no clinical phenotype has been associated with its development.
Al-Hammadi, Noor +4 more
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Calcinosis and myocarditis in systemic lupus erythematosus patient
Indonesian Journal of Rheumatology, 2018 Systemic lupus erythematosus (SLE) patients have multi-organ involvement related to their chronic inflammatory, autoimmune disease. Calcinosis can be clinical manifestations of SLE.
Sumartini Dewi, Rachmat Gunadi Wachjudi
doaj +1 more source
An Unusual Combination of Neurological Manifestations and Sudden Vision Loss in a Child with Familial Hyperphosphatemic Tumoral Calcinosis [PDF]
, 2019 Hyperphosphatemia in the absence of renal failure is an unusual occurrence, particularly in children, but is a common primary feature of familial hyperphosphatemic tumor calcinosis.
Acton, Dena +7 more
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