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Hyperphosphatemic Tumoral Calcinosis: Pathogenesis, Clinical Presentation, and Challenges in Management [PDF]

Frontiers in Endocrinology, 2020
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare and disabling disorder of fibroblast growth factor 23 (FGF23) deficiency or resistance.
Rachel I Gafni
exaly   +5 more sources

Pre-patellar Tumoral Calcinosis of Knee with Intra-articular Extension: An Index Case Study [PDF]

Journal of Orthopaedic Case Reports
Introduction: Tumoral calcinosis is a rare hereditary condition characterized by the deposition of calcium phosphate and hydroxyapatite in periarticular soft tissues.
Manoj Kumar, Reddy Lakshmana Sai, Tufan Mandal, Kumar Keshav, Hari Kishan, Theynesh Kumar P   +5 more
doaj   +3 more sources

Tumoral calcinosis in the extensor indicis proprius tendon: A case report [PDF]

Clinical Case Reports, 2023
Key Clinical Message Tumoral calcinosis is a rare clinicopathological entity characterized by the presence of calcified deposits in the periarticular soft tissue.
Maithaa AlShamsi, Ammar AlDhamin
doaj   +3 more sources

Tumoral calcinosis of unusual location in a chronic hemodialysis patient [PDF]

BJR Case Rep, 2023
Tumoral calcinosis is a rare cause of intratissular calcifications in hemodialysis patients with chronic renal failure. Its frequency is estimated between 0.5 and 7% of patients. We illustrate through a case of unusual localization diagnosed in Ibn Rochd
Youssef Sakhy, Réda Taoussi, Vianney Ndayishimiye, Mouna Sabiri, Mohammed Labied, Ghizlane Lembarki, Samia El Manjra, Samira Lezar, Fatiha Essodegui   +8 more
semanticscholar   +3 more sources

Idiopathic Tumoral Calcinosis [PDF]

Journal of the Belgian Society of Radiology, 2021
Teaching Point: The imaging clues to differentiate idiopathic tumoral calcinosis from other calcified soft tissue lesions include: pseudotumoral appearance with mass effect, bone erosion with intra-osseous protrusion of calcification, lobulated ...
Jesper Dierickx, Filip Vanhoenacker
doaj   +8 more sources

Case report of tumoral calcinosis in a peritoneal dialysis patient with tertiary hyperparathyroidism and systemic lupus erythematosus [PDF]

Clinical Case Reports
Key Clinical Message Tumoral calcinosis (TC) is a rare condition characterized by dystrophic calcinosis. TC in end stage kidney disease is associated with severe hyperparathyroidism.
Kalpa Jayanatha, Irfan Idrus, Mark Sapsford, Viliami Tutone, Michael Lam   +4 more
doaj   +3 more sources

GALNT3 Mutation in Hyperphosphatemic Familial Tumoral Calcinosis – Novel Etiology of Secondary Amyloidosis [PDF]

Indian J Nephrol
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.
Sourabh Sharma, Sahil Arora, Renju Binoy, Anupam Agarwal, Pallavi Prasad, Himanshu Verma   +5 more
semanticscholar   +3 more sources

Pathologic Fracture of Femoral Neck in a Patient with Tumoral Calcinosis [PDF]

Hip Pelvis, 2022
Tumoral calcinosis is a rare disease characterized by massive subcutaneous soft tissue deposits of calcium phosphate around large joints in patients with chronic kidney disease. Invasion of bone by tumoral calcinosis is rare.
Seong-San Park, Soo Jae Yim, Sin Hyung Park   +2 more
semanticscholar   +3 more sources

The Successful Treatment of Deep Soft-tissue Calcifications with Topical Sodium Thiosulphate and Acetazolamide in a Boy with Hyperphosphatemic Familial Tumoral Calcinosis due to a Novel Mutation in FGF23

JCRPE, 2022
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare autosomal recessive disorder. Topical sodium thiosulfate (STS) and acetazolamide can be a safe and effective treatment for patients who do not respond to conventional therapy for ectopic ...
Hakan Döneray, Ayşe Özden, Kadri Gürbüz   +2 more
doaj   +3 more sources

A Sole Case of the FGF23 Gene Mutation c.202A>G (p.Thr68Ala) Associated with Multiple Severe Vascular Aneurysms and a Hyperphosphatemic Variant of Tumoral Calcinosis—A Case Report [PDF]

Life
Tumoral calcinosis is an extremely rare genetic disease caused by mutations in three genes, GALNT3, FGF23, and KL, which disrupt phosphorus metabolism. The hallmark of this condition is the formation of tumors in the soft tissues around the joints. Other
Nevena Georgieva Ivanova
doaj   +3 more sources