Different outcomes following parathyroidectomy in patients with uremic tumoral calcinosis: two case reports. [PDF]
Background Uremic tumoral calcinosis (UTC) is a rare complication in hemodialysis patients, whose mechanism remains incompletely understood.
Li J, Li X, Dong X, Ma L, Guo Z, Chen X.
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A rare disease: Familial hyperphosphatemic tumoral calcinosis [PDF]
Introduction Tumoral calcinosis (TC) is a rare disease characterized by soft tissue calcification as a result of repetitive trauma and prolonged pressure in periarticular areas of large joints; such as hip, knee, shoulder and elbow.
Seçkin Akçay +2 more
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7984 A Challenging Case Of Hyperphosphatemic Familial Tumoral Calcinosis [PDF]
Disclosure: T.G. de Souza: None. T.J. Weber: None. Introduction: Hyperphosphatemic Familial Tumoral Calcinosis (hFTC) is a rare, autosomal recessive metabolic disorder characterized by elevated serum phosphate levels and the accumulation of calcium ...
T. G. de Souza, Thomas Joseph Weber
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Avid 18F-FDG Uptake in Idiopathic Tumoral Calcinosis Mimicking Lymph Node Metastasis [PDF]
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
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Objective. Uraemic tumoral calcinosis refers to metastatic calcifications that occur rarely on the extensor surfaces of joints in patients undergoing long-term haemodialysis.
F E Suleman, V Mngomezulu, N Ebrahim
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Prepatellar tumoral calcinosis mimicking soft tissue sarcoma: A case report and review of literature
Tumoral calcinosis is a rare, painless tumour-like mass often seen as soft tissue calcifications around joints in adolescents and young adults. The occurrence of this rare entity in the middle aged or elderly population is also rare.
Dim EM +5 more
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Structural and molecular imaging-based characterization of soft tissue and vascular calcification in hyperphosphatemic familial tumoral calcinosis. [PDF]
Hyperphosphatemic Familial Tumoral Calcinosis (HFTC) is a rare disorder caused by deficient FGF23 signaling and resultant ectopic calcification. In this study, we systematically characterized and quantified macro- and micro-calcification in an HFTC ...
Sheppard AJ +8 more
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Navigation-assisted resection of tumoral calcinosis of the lumbosacral spine: illustrative case. [PDF]
BACKGROUND Tumoral calcinosis is an uncommon disease resulting from dystrophic calcium phosphate crystal deposition, with only 7% of cases involving the spine, and it may diagnostically mimic neoplasms. OBSERVATIONS In this case, a 54-year-old woman with
Tang OY +6 more
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GALNT3 Mutation in Hyperphosphatemic Familial Tumoral Calcinosis - Novel Etiology of Secondary Amyloidosis. [PDF]
Tumoral calcinosis is a rare syndrome characterized by calcium salt deposition in different periarticular soft tissue regions. We report this case of tumoral calcinosis with history of persistent soft tissue calcifications for over three decades.
Sharma S +5 more
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Spatial Atlas for Mapping Vascular Microcalcification Using 18F-NaF PET/CT: Application in Hyperphosphatemic Familial Tumoral Calcinosis. [PDF]
BACKGROUND: Vascular calcification causes significant morbidity and occurs frequently in diseases of calcium/phosphate imbalance. Radiolabeled sodium fluoride positron emission tomography/computed tomography has emerged as a sensitive and specific method
Sheppard AJ +10 more
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