Síndrome de QT largo y taquicardia ventricular en torsade de pointes secundarios a hipopituitarismo: una asociación a tener en cuenta. Caso clínico

• Autores: José Miguel García Castro, Antonia García Martín, Emilio Guirao Arrabal, Pedro Luis Carrillo Alascio
• Localización: Revista Médica de Chile, ISSN-e 0034-9887, Vol. 145, Nº. 7, 2017, págs. 941-944
• Idioma: español
• Títulos paralelos:
  • Long QT syndrome and polymorphic ventricular tachycardia due to hypopituitarism. Report of one case
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• Resumen

  • Symptoms of hypopituitarism are usually chronic and nonspecific, but rarely the disease can have acute and life threatening manifestations. We report a 53 years old female with a pituitary adenoma that was admitted to our hospital because of syncope. The electrocardiogram showed sinus bradycardia with a prolonged QT interval. Frequent runs of non-sustained polymorphic ventricular tachycardia were noted on telemetry. The patient had a history of severe acute headaches in the previous days and laboratory tests revealed severe secondary hypothyroidism, adrenal insufficiency and a decrease in pituitary hormones. A magnetic resonance imaging of the head showed changes in the size and contrast enhancement of the adenoma. A diagnosis of hypopituitarism secondary to pituitary apoplexy was made and treatment with hydrocortisone and, subsequently, levothyroxine was started. Hormonal disorders such as hypothyroidism, adrenal insufficiency or hypopituitarism should be considered as unusual causes for reversible cardiomyopathy, long QT syndrome and ventricular arrhythmias.