ASSOCIATION BETWEEN PRIMARY HYPERPARATHYROIDISM AND PARATHYROID GLAND ADENOMA (Atena Editora)

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MetadadosDescriçãoIdioma
Autor(es): dc.contributor.authorDotto, João Francisco Pozzebon-
Data de aceite: dc.date.accessioned2024-08-13T18:24:26Z-
Data de disponibilização: dc.date.available2024-08-13T18:24:26Z-
Data de envio: dc.date.issued2024-08-05-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/868831-
Resumo: dc.description.abstractmetabolism. Typically, it is characterized by hypercalcemia and elevated serum concentrations of parathyroid hormone (PTH), the hormone produced by the parathyroid glands. Most cases of primary hyperparathyroidism occur due to an adenoma of the parathyroid glands (85% of cases). Biochemical screening tests, introduced in the 1970s, made it possible to diagnose the disease earlier, even in the asymptomatic phase. The disease can be diagnosed at a symptomatic stage, typically in countries where screening tests are not common. In the symptomatic phase, the disease can cause bone loss, kidney stone formation, as well as gastrointestinal, cardiovascular and neuropsychiatric manifestations. Primary hyperparathyroidism may present with serum calcium concentration within the normal range, but with parathyroid hormone at levels above the normal limit. Diagnosis of the disease involves clinical manifestations, laboratory tests and imaging tests, with ultrasound and 99mTc-sestamibi scintigraphy being the most commonly used imaging methods. The only treatment that can cure the disease is parathyroidectomy, in which one or more parathyroid glands are removed. Surgery allows an increase in bone mineral density and reduces the incidence of nephrolithiasis. For patients who do not undergo surgery, monitoring of serum calcium concentrations and bone mineral density is indicated.pt_BR
Idioma: dc.language.isoenpt_BR
Palavras-chave: dc.subjecthyperparathyroidismpt_BR
Título: dc.titleASSOCIATION BETWEEN PRIMARY HYPERPARATHYROIDISM AND PARATHYROID GLAND ADENOMA (Atena Editora)pt_BR
Tipo de arquivo: dc.typelivro digitalpt_BR
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