Mf. Abdulmohsen et Ai. Alsultan, PANHYPOPITUITARISM, HYPONATREMIA AND LONG QT INTERVAL SYNDROME - A CASE-REPORT, Saudi medical journal, 17(4), 1996, pp. 531-535
Acquired prolongation of QT interval in the conventional electrocardio
gram has been reported in many medical problems including coronary art
ery disease, mitral valve prolapse, drug idiosyncracies especially ant
iarrhythmic and psychotropic drugs, electrolyte disturbances and endoc
rine abnormalities as in hypothyroidism. However, there is a body of e
vidence in the literature indicating that this problem is relatively u
ncommon in simple cases of hypothyroidism. We report a 60 year old Sau
di patient who was transferred from the regular ward to the Coronary C
are Unit (CCU) with severe hyponatremia, clinical manifestration of pa
nhypopituitarism and prolonged QTc (730 ms). She developed a short par
oxysm of Torsades-de-Pointes ventricular tachycardia early after the t
ransfer to the CCU. Panhypopituitarism was documented through specific
endocrinological investigations. The prolongation of QT interval and
the hyponatremia were normalized shortly after the initiation of hormo
nal replacement therapy. We feel that adrenocortical insufficiency as
a part of panhypopituitarism is a probable contributory factor in the
development of this electrophysiological abnormality.