Atypical hemolytic uremic syndrome (HUS) is a heterogeneous group of disord
ers, the pathogenesis of which is unclear. Plasma transfusions and plasmaph
eresis are widely used modes of therapy for adults with this life threateni
ng syndrome. There is very limited experience in using plasmapheresis thera
py in children and infants with atypical HUS. Plasmapheresis, which is cons
idered a relatively safe procedure in adults and older children, may be haz
ardous in neonates and very young infants and can result in severe complica
tions. We report a 2-month-old infant with idiopathic atypical HUS, who was
successfully treated with a 1-month course of plasmapheresis during the ac
ute phase of the disease. Appropriate preparations as well as several adjus
tments were made in order to meet the special needs of this very young infa
nt who, to the best of our knowledge, is the youngest reported patient with
atypical HUS to undergo plasmapheresis. Plasmapheresis therapy of the infa
nt was not associated with any complications of the procedure and resulted
in marked clinical improvement. We conclude that plasmapheresis in neonates
and in very small infants is technically feasible, can be performed withou
t major complications, and may be of benefit in individual cases.