Pure red-cell aplasia is an anemia characterized by a near absence of
nucleated red blood cells, It can be congenital or acquired. The conge
nital form is probably induced by intrauterine damage to early erythro
id stem cells, The acquired form can be transient and self-limited or
sustained and lifelong, Many, if not most, cases of transient pure red
-cell aplasia are caused by the B19 parvovirus, which has a special af
finity for erythroid progenitor cells, When complicating an underlying
hemolytic anemia, the anemia may be acute and severe. Sustained aplas
ia is caused by viral invasion, immune rejection or toxic destruction
of progenitor or precursor cells. It occurs most often in patients wit
h a benign or malignant lymphoid disease, Treatment with immunosuppres
sive drugs - especially corticosteroids - will in most cases cause a t
emporary or permanent remission, The final outcome depends primarily o
n the underlying disorder.