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Some of the next articles are maybe not open access.
Tropical Doctor, 2006
Tumoral calcinosis is a rare, benign disease that commonly affects the African blacks. We report on a 20-year-old Nigerian presenting with recurrent multiple subcutaneous masses around the scapular, elbow, hip and gluteal regions. The X-rays, fine needle aspiration cytology and tissue biopsy confirmed the diagnosis and the patient had a successful ...
H A, Nggada +5 more
openaire +2 more sources
Tumoral calcinosis is a rare, benign disease that commonly affects the African blacks. We report on a 20-year-old Nigerian presenting with recurrent multiple subcutaneous masses around the scapular, elbow, hip and gluteal regions. The X-rays, fine needle aspiration cytology and tissue biopsy confirmed the diagnosis and the patient had a successful ...
H A, Nggada +5 more
openaire +2 more sources
Scottish Medical Journal, 2014
Introduction Tumoral calcinosis is a rare condition characterised by progressive, ectopic, periarticular deposits of calcium. These tumour-like growths often infiltrate muscle and tendon, usually presenting as multiple masses or as a painless, solitary mass.
Amal, Alkhatib +2 more
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Introduction Tumoral calcinosis is a rare condition characterised by progressive, ectopic, periarticular deposits of calcium. These tumour-like growths often infiltrate muscle and tendon, usually presenting as multiple masses or as a painless, solitary mass.
Amal, Alkhatib +2 more
openaire +2 more sources
Hyperphosphatemic Familial Tumoral Calcinosis
Southern medical journal (Birmingham, Ala. Print)Hyperphosphatemic familial tumoral calcinosis is an autosomal recessive condition that requires a multidisciplinary approach, not only to reach an accurate diagnosis but also for treatment.
Margaret Kaszycki +7 more
semanticscholar +1 more source
Australasian Journal of Dermatology, 2021
Calciphylaxis is a potencially disorder in patients with hyperphosphatemic familial tumoral calcinosis (HFTC). Patients commonly present livedo racemosa and retiform purpura, which may progress to necrosis and very painful ulcers.
Sheila Requena +3 more
semanticscholar +1 more source
Calciphylaxis is a potencially disorder in patients with hyperphosphatemic familial tumoral calcinosis (HFTC). Patients commonly present livedo racemosa and retiform purpura, which may progress to necrosis and very painful ulcers.
Sheila Requena +3 more
semanticscholar +1 more source
Journal of Pediatric Endocrinology & Metabolism (JPEM), 2021
Objectives Familial hyperphosphatemic tumoral calcinosis is a rare disorder characterized by hyperphosphatemia with recurrent ectopic periarticular calcifications, in addition to other visceral and vascular manifestations, without any inflammatory or ...
Merve Emecen Şanlı +6 more
semanticscholar +1 more source
Objectives Familial hyperphosphatemic tumoral calcinosis is a rare disorder characterized by hyperphosphatemia with recurrent ectopic periarticular calcifications, in addition to other visceral and vascular manifestations, without any inflammatory or ...
Merve Emecen Şanlı +6 more
semanticscholar +1 more source
Tumoral Calcinosis with an Atypical Presentation in the Foot: A Case Report.
Journal of the American Podiatric Medical Association (Print)Tumoral calcinosis is a rare disorder defined as the development of periarticular calcified masses, typically surrounding large joints, although they may occur in the foot.
Thomas Ehlers +3 more
semanticscholar +1 more source
Tumoral Calcinosis (Calcinosis Circumscripta) in the Horse
Journal of the American Veterinary Medical Association, 1970SUMMARY The characteristic feature of tumoral calcinosis in 6 horses was the development of hard subcutaneous multiloculated nodules that consisted of amorphous calcified material. In 5 horses the nodules were near the tibiofibular joint. Surgical removal of the lesion was attempted in 3 horses and was accomplished with ease in 2.
D C, Dodd, C W, Raker
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Clinical Nephrology, 2021
We report a case of a 32-year-old man who was undergoing chronic hemodialysis and had hyperphosphatemia and secondary hyperparathyroidism (SHPT) with multiple tumoral calcinosis (TC) lesions refractory to drug therapy.
Tomohiro Saito +10 more
semanticscholar +1 more source
We report a case of a 32-year-old man who was undergoing chronic hemodialysis and had hyperphosphatemia and secondary hyperparathyroidism (SHPT) with multiple tumoral calcinosis (TC) lesions refractory to drug therapy.
Tomohiro Saito +10 more
semanticscholar +1 more source
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1990
Tumoral calcinosis is a distinct entity, which is rarely seen in Europe and North America but much more common in black Africans. Typical symptoms are calcified nodules, which grow while remaining asymptomatic and are found in the tissues adjacent to the large joints of the body.
J, Zimmermann, W, Hartschuh, D, Petzoldt
openaire +1 more source
Tumoral calcinosis is a distinct entity, which is rarely seen in Europe and North America but much more common in black Africans. Typical symptoms are calcified nodules, which grow while remaining asymptomatic and are found in the tissues adjacent to the large joints of the body.
J, Zimmermann, W, Hartschuh, D, Petzoldt
openaire +1 more source