Hipocalcemias
- Calatayud Gutiérrez, María
- Allo Miguel, G.
ISSN: 0304-5412
Año de publicación: 2012
Título del ejemplar: Enfermedades endocrinológicas y metabólicas: patología del metabolismo fosfocálcico
Serie: 11
Número: 16
Páginas: 944-950
Tipo: Artículo
Otras publicaciones en: Medicine: Programa de Formación Médica Continuada Acreditado
Resumen
The most common clinical presentation of primary hyperparathyroidism (HPPl is asymptomatic hypercalcemia. Measurement of serum intact paratohormone (iPTHl is necessary to diagnose primary hyperparathyroidism (HPPL in patients with vitamin O in the normal range. HPP Surgery criteria includes serum calcium concentration >1.0 mg/dL above the upper limit of normal, creatinine clearance < 60 mL/min, T score < -2.5 at any level and age less than 50 years. Normocalcemic hyperparathyroidism is a new variant of hyperparathyroidism, which must be confirmed at least two times. It must be diagnosed by exclusion of other causes of secondary hyperparathyroidism. Natural history of asymptomatic and normocalcemic HPP notes that it usually does not evolve to hypercalcemia. Hypoparathyroidism presents hypocalcemia and low level of PTH. The condition can be inherited, but it is usually encountered after thyroid or parathyroid gland surgery, and it can be caused by immune system-related damage as well as a number of rarer causes. The diagnosis is made with blood tests, and other investigations such as genetic testing depending on the results. The treatment of hypoparathyroidism consists ofcalcium replacement and vitamin D.