A 7-year-old girl developed pure red cell aplasia during carbamazepine
(CBZ) monotherapy for epilepsy. She developed generalized clonic conv
ulsions at the age of 7 years and 8 months. Treatment with CBZ was beg
un. Two months later she was admitted to our hospital because of sever
e anemia. Bone marrow examination revealed the almost complete absence
of erythroblasts, with normal myelopoiesis and megakaryocytopoiesis,
indicating pure red cell aplasia. Following the discontinuation of CBZ
, she developed brisk reticulocytosis within 1 week and her hemoglobin
level rose to a normal one within 1 month. Although the hematological
toxicity of CBZ is well documented, isolated cessation of red cell pr
oduction is uncommon. A patient who is undergoing treatment with CBZ s
hould be carefully monitored, especially for serious adverse reactions
including pure red cell aplasia. (C) 1997 Elsevier Science B.V.