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1.
BMJ Case Rep ; 20172017 Jul 27.
Artigo em Inglês | MEDLINE | ID: mdl-28751432

RESUMO

Hypokalaemic paralysis covers a heterogeneous group of disorders caused either by an enhanced shift of potassium into the cells or following a significant renal or gastrointestinal loss of potassium. We present the case of a 48-year-old Caucasian man with paralysis of both upper and lower extremities. ECG showed sinus rhythm and characteristic changes of hypokalaemia with depression of the ST segment, prolonged QTc interval of 581ms and U waves seen as a small positive deflection at the T wave in the middle precordial leads. We suspected the cause of hypokalaemia leading to paralysis to be due to administration of high doses of furosemide without oral potassium supplementation coupled with regular use of insulin. Initial therapy included both oral and intravenous potassium replacement and close monitoring of cardiac rhythm and serum potassium levels. Twenty-four hours after admission, the potassium level had normalised and the patient slowly recovered and gained strength. The patient was discharged after 1 week of careful follow-up and did not experience any serious degree of rebound hyperkalaemia. At the time of discharge, all laboratory tests were normal and ECG revealed a normal sinus rhythm and normal QTc intervals.


Assuntos
Arritmias Cardíacas/induzido quimicamente , Diuréticos/efeitos adversos , Furosemida/efeitos adversos , Paralisia Periódica Hipopotassêmica/induzido quimicamente , Paralisia Periódica Hipopotassêmica/fisiopatologia , Insulina/efeitos adversos , Potássio/sangue , Administração Intravenosa , Diuréticos/administração & dosagem , Furosemida/administração & dosagem , Humanos , Paralisia Periódica Hipopotassêmica/sangue , Insulina/administração & dosagem , Masculino , Pessoa de Meia-Idade , Potássio/uso terapêutico , Doenças Raras , Recuperação de Função Fisiológica , Resultado do Tratamento
2.
BMJ Case Rep ; 20162016 Dec 20.
Artigo em Inglês | MEDLINE | ID: mdl-27999128

RESUMO

Blue rubber bleb naevus syndrome (BRBNS) is a rare vascular disorder with malformed veins, or blebs, appearing in the skin or internal organs. Gastrointestinal tract involvement is the most common feature and often subject to bleeding, potentially resulting in chronic occult blood loss and iron deficiency anaemia. We present the case of a 10-year-old boy with venous malformations on the feet and severe anaemia. Although massive sudden haemorrhage rarely occurs, awareness of the illness is necessary to prevent complications.


Assuntos
Anemia Ferropriva/etiologia , Hemorragia Gastrointestinal/etiologia , Neoplasias Gastrointestinais/complicações , Nevo Azul/complicações , Neoplasias Cutâneas/complicações , Anemia Ferropriva/diagnóstico , Criança , Endoscopia Gastrointestinal , Hemorragia Gastrointestinal/diagnóstico , Neoplasias Gastrointestinais/diagnóstico , Humanos , Masculino , Nevo Azul/diagnóstico , Neoplasias Cutâneas/diagnóstico
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