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Przegl Lek ; 71(4): 210-4, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25141580

RESUMO

Tumor lysis syndrome (TLS) occurs as a result of massive lysis of malignant cells and release of intracellular contents into the systemic circulation. It can lead to hyperuricaemia, hyperkalaemia, hyperphosphataemia and hypocalcaemia. TLS is most commonly present after initiation of anticancer therapy but it can also develop spontaneously (STLS--spontaneous tumor lysis syndrome). In the article, pathophysiology, classification, risk factors and recommendations of management in TLS, with a special focus on solid tumors, are discussed. The keys to the identification of high-risk patients, prevention and management of TLS are included in presented guidelines.


Assuntos
Síndrome de Lise Tumoral/diagnóstico , Síndrome de Lise Tumoral/terapia , Causalidade , Emergências , Humanos , Guias de Prática Clínica como Assunto , Síndrome de Lise Tumoral/epidemiologia
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