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Tumoral calcinosis is a rare complication in uremic patients. An in-depth review of published literature suggests that most patients with uremic tumoral calcinosis do not respond to medical treatment.
Yaerim Kim, Eunah Hwang, Sungbae Park
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Tumoral calcinosis is a rare autosomal recessive disorder marked by lobulated soft tissue calcifications not associated with physiologic osteogenesis but rather phosphate metabolism dysregulation.
Derek T. Clar+2 more
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Tumoral calcinosis of the hand
Tumoral calcinosis is a rare condition described in literature as a deposition of calcium salts in soft tissues. We here report a rare case of Tumoral calcinosis in the index finger of a hand in a 22-year-old woman. Because of the absence of any trauma, normal serum phosphate and calcium levels and no symptoms but a cosmetic defect, our case is ...
AMATI, CARLO+4 more
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Multimodal imaging in the differential diagnosis of soft tissue calcinosis
Soft tissue calcinosis is a common radiographic finding, which may be related to different types of pathological processes. Multimodality imaging, combined with analysis of clinical and laboratory data, plays an important role for the differential ...
G. Garlaschi+6 more
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Familial tumoral calcinosis in two Chinese patients: a case series
Introduction Tumoral calcinosis is a rare and benign condition characterized by massive subcutaneous soft tissue deposits of calcium phosphate predominantly around large joints.
Cheng Xiaoli+3 more
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Calcinosis of the internal jugular vein: Interesting presentation of tertiary hyperparathyroidism
Tumoral calcinosis is a severe complication of hemodialysis. A 49‐year‐old male on dialysis for end‐stage renal disease developed a large calcified retropharyngeal mass. This caused stridor and dyspnea, necessitating an emergency awake tracheostomy. This
Courtney B. Shires, Mona Shete
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Huge tumoral calcinosis mimicking a sarcoma
Asha Sharad Shenoy+2 more
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Bone Involvement in Hyperphosphatemic Familial Tumoral Calcinosis: A New Phenotypic Presentation. [PDF]
Mutations in FGF23, KL, and GALNT3 have been identified as the cause for the development of hyperphosphatemic familial tumoral calcinosis (HFTC). Patients with HFTC typically present in childhood or adolescence with periarticular soft tissue deposits ...
Freedman JD+4 more
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Tumoral calcinosis of bilateral hip joint in an adult female: A Case report [PDF]
The term Tumoral Calcinosis (TC) was coined by Inclan in 1943 but similar pathological entities were recognized in the late 1890s [1,2]. It is a rare condition consisting of accumulation of calcium in periarticular tissue outside of capsule.
F. Byiringiro Mugabe, B. Rugwizangoga
doaj
Parathyroid hormone (PTH) and fibroblast growth factor 23 (FGF23) both influence blood phosphate levels by regulating urinary phosphate reabsorption. Clinical data suggest that adequate renal phosphate handling requires the presence of both FGF23 and PTH,
D. Ovejero+6 more
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