Zobrazeno 1 - 10
of 1 061
pro vyhledávání: '"Oncogenic osteomalacia"'
Autor:
Jose Malagon‐Rangel, Jose Gabriel Solis, Luis Fernando Zavala‐Jonguitud, Martín Roberto Basile‐Alvarez, Andrea Malagon‐Liceaga
Publikováno v:
Clinical Case Reports, Vol 11, Iss 12, Pp n/a-n/a (2023)
Key Clinical Message Tumor‐induced osteomalacia is a paraneoplastic syndrome characterized by renal phosphate wasting and deranged bone turnover. Clinicians should consider tumor‐induced osteomalacia in unexplained hypophosphatemia and investigat
Externí odkaz:
https://doaj.org/article/150c6d6fe0c94992b7ec0fd0cf9fa34c
Akademický článek
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Akademický článek
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Autor:
Agnieszka Brociek-Piłczyńska, Dorota Brodowska-Kania, Kornel Szczygielski, Małgorzata Lorent, Grzegorz Zieliński, Piotr Kowalewski, Dariusz Jurkiewicz
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Tumor-induced osteomalacia (TIO) is a rare, acquired disease of renal phosphate wasting and disturbed vitamin D homeostasis as a result of the action of a phosphaturic protein – FGF-23, produced by a neoplasm. Although the clini
Externí odkaz:
https://doaj.org/article/491fb14d6adc41bab6a965976d8c3d09
Autor:
M. Moreno Romero, I. Pérez Muñoz, F. González Lizán, J.I. Gallego Rivera, L. Valdivielso Cañas
Publikováno v:
Revista Española de Cirugía Ortopédica y Traumatología, Vol 65, Iss 6, Pp 443-450 (2021)
Resumen: Introducción: El tumor mesenquimal fosfatúrico (TMF) es una causa poco frecuente de osteomalacia oncogénica (OO), síndrome paraneoplásico que puede cursar con clínica severa en el aparato locomotor. El TMF es una neoplasia mesenquimal
Externí odkaz:
https://doaj.org/article/d3f3883a11164397b9c37b0475ffd0bc
Autor:
Camila R. Muniz, Gabriela A. M. Bezerra, Viviane C. da Silva, Priscilla M. F. Aguiar, Gunter Gerson, Catarina B. D’Alva, André A. A. Nunes
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-5 (2021)
Abstract Background Glomangioma is a benign tumor of mesenchymal origin, derived from the glomus body. It is responsible for the thermal regulation of the dermis. The occurrence of oncogenic osteomalacia related to glomangioma is rare. Only two cases
Externí odkaz:
https://doaj.org/article/20be530cd5bf4cc6a19cab66be0ba844
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-5 (2021)
Introduction: Oncogenic osteomalacia (Onc-Ost) is a paraneoplastic phenomenon characterized by hypophosphatemia due to elevated fibroblast growth factor-23 (FGF-23). Onc-Ost has been previously reported in patients with germ line mesenchymal tumors a
Externí odkaz:
https://doaj.org/article/f22c701bea29437cb4c6fa395aa116d3
Publikováno v:
Endocrine Regulations, Vol 55, Iss 3, Pp 163-168 (2021)
Objective. Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome characterized by chronic hypophosphatemia and osteomalacia. We present case of a patient with a protracted clinical course of TIO. TIO profoundly affected every aspect of h
Externí odkaz:
https://doaj.org/article/dc01d760f1514710b80310e423e51c0d
Publikováno v:
Travmatologiâ i Ortopediâ Rossii, Vol 27, Iss 2, Pp 114-123 (2021)
Background. The rarity of the disease and, in this regard, the lack of doctors awareness about the pathology, late diagnosis and severe complications of the musculoskeletal system emphasize the relevance of clinical case demonstrating. The uniqueness
Externí odkaz:
https://doaj.org/article/3dae5cc2a2c146bf914ee39969432462
Autor:
Anna K. Eremkina, Svetlana S. Mirnaya, Anna M. Gorbacheva, Taras S. Panevin, Iya A. Voronkova, N. G. Mokrysheva
Publikováno v:
Ожирение и метаболизм, Vol 17, Iss 2, Pp 220-227 (2020)
Osteomalacia is a systemic bone disease, characterized by an excessive accumulation of non-mineralized osteoid and an imbalance in the organic matrix formation and mineralization. A rare cause of disease is tumor-induced osteomalacia, most often due
Externí odkaz:
https://doaj.org/article/e26049fdd91041fdb269aa55f6bc9e99