Although rare, amyloidosis and hemochromatosis are the infiltrative di
seases in which the heart is more frequently involved. The most common
clinical presentation is heart failure with hemodynamic features of r
estrictive heart disease in cardiac amyloidosis. The diagnosis is ofte
n made because of symptoms of other organ involvement, although someti
mes cardiac symptoms may be the initial manifestation. The non-specifi
c clinical presentation and the low prevalence of these cardiomyopathi
es make the diagnosis difficult if the clinician does not suspect it.
Once symptoms develop, the evolution is fast. Usually, the unsatisfact
ory and ineffective treatment of amyloidosis and hemochromatosis contr
ibute to the poor prognosis. The indication of cardiac transplantation
in advanced cases is questionable because of the high recurrence of t
he illness.