Results 121 to 130 of about 2,912,781 (218)
Calcified or ossified benign soft tissue lesions that may simulate malignancy [PDF]
The purpose of this article is to review calcified or ossified benign soft tissue lesions that may simulate malignancy. We review the clinical presentations, locations, imaging characteristics, and differential diagnostic considerations of myositis ...
Kwee, Robert M., Kwee, Thomas C.
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Laxative related primary hyperphosphatemic tumoral calcinosis identified by bone scintigraphy
We describe a case of a 40-year-old female patient presenting with tumor calcinosis where hypertrophic pulmonary osteoarthropathy (HPOA) was suspected given her extensive history of malignancy.
Marcus Asokendaran, Nat Lenzo
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Improved hypercalcemia after debulking of uremic tumoral calcinosis in a parathyroidectomized patient. [PDF]
Uremic Tumoral Calcinosis (UTC) is a rare complication of chronic kidney disease on dialysis, characterized by large periarticular calcification. Among some cases, hypercalcemia with no conventional etiologies has been reported.
Bornemann, Michael +2 more
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Tumoral calcinosis in an 8-year-old girl: A case report
Introduction: Tumoral Calcinosis is a rare, benign metabolic disorder, characterized by the deposition of calcium phosphate crystals in extra-articular soft tissues.
M. Savadier, N. Maistry, D.S. Harrison
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Tumoral calcinosis with vitamin D deficiency
A 50-year-old woman presented with recurrent calcified mass in the left gluteal region. The clinical, radiological, and biochemical profile confirmed the diagnosis of tumoral calcinosis. She also had associated vitamin D deficiency. The patient underwent
Kannan Subramanian +6 more
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This case report describes intense F-18 fluorodeoxyglucose (FDG) uptake within two foci of secondary tumoral calcinosis, incidentally noted during the workup of small-cell lung cancer.
Dennis M. Duryea, DO +2 more
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Tumoral calcinosis: a case report
Tumoral calcinosis is a rare disorder with the calcified masses in subcutaneous tissues. We report herein a nine-year-old girl, in whom the calcified lesions bilaterally involved the soft tissues in the anterior part of the knee joint.
I Ozkan +5 more
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Inactivating autosomal recessive mutations in fibroblast growth factor 23 (FGF23), klotho (KL) and polypeptide N-acetylgalactosaminotransferase 3 (GALNT3) genes lead to a rare disorder, hyperphosphatemic familial tumoral calcinosis (HFTC).
Rabia Miray Kışla Ekinci +6 more
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Acute tumoral calcinosis due to severe hyperphosphatemia in a maintenance hemodialysis patient [PDF]
Keizo Nishime, Hiroki Takahashi
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