Results 71 to 80 of about 19,007 (183)
Hypophosphatemic rickets: A case of recurrent pathological fractures
Indian Journal of Endocrinology and Metabolism, 2012 Introduction: Renal phosphate-wasting disorders are the most common form of hereditary rickets and osteomalacia in western countries, but are rarely reported in India. Therefore, we report here a case of hypophosphatemic rickets.
Arjun Baidya +3 more
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Indian Journal of Radiology and Imaging, 2017 The somatostatin (SS) receptor scintigraphy (SRS), using octreotide radiolabelled with 111In (Ocreoscan©, OCT), is a consolidated diagnostic procedure in patients with neuroendocrine tumors (NET) because of an increased expression of somatostatin ...
Vincenzo Cuccurullo +3 more
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Proceedings of the Royal Society of Medicine, 1969 C K, Connolly, J R, Nassim
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Journal of Cancer Research and Therapeutics, 2009 Oncogenous osteomalacia is a rare paraneoplastic renal phosphaturic condition, often associated with highly vascular benign mesenchymal tumors. We report a case of a 48-year-old male who presented with debilitating osteomalacia unresponsive to standard therapy.
Ghosh, Soumitra +3 more
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Familial vitamin D deficient osteomalacia and renal osteodystrophy: Shaping up the debate
Saudi Journal of Kidney Diseases and Transplantation, 2010 Osteomalacia is a common occurrence world over due to the deficiency in vitamin D and calcium intake. We present here two sisters with features of sever osteomalacia, myopathy and hypophosphatemia hyperparathryroidism and 25(OH)D2, 25(OH)D3and 1,25(OH)D3
Jabur Wael
doaj
Case Report: Phosphaturic mesenchymal tumor presenting solely as knee pain without hypophosphatemia
Frontiers in OncologyPhosphaturic mesenchymal tumor (PMT) is a rare tumor disease that often leads to tumor-induced osteomalacia (TIO). The typical manifestations of this disease include hypophosphatemia and osteomalacia. The main symptom in most PMT patients is diffuse pain
Qianqian Cao, Cheng Cheng, Zhipeng Dai
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Tumor-induced phosphopenic osteomalacia: modern approaches to diagnostics and treatment
Современная ревматологияPhosphopenic osteomalacia (PPOM) is a rare variant of paraneoplastic syndrome caused by tumor synthesis of fibroblast growth factor 23 (FGF23). FGF23 secretion leads to a decrease in phosphate reabsorption and calcitriol levels, which leads to the ...
A. A. Kondrashov +4 more
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An unusual cause of osteomalacia in a young lady
Annals of Medical Science and ResearchOncogenic osteomalacia is a rare entity, caused by excessive secretion of fibroblast growth factor-23 (FGF-23) from the peripherally located benign tumours of mesenchymal origin.
Angan Karmakar +3 more
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