O. Huter et al., SUCCESSFUL TREATMENT OF PREGNANCY-ASSOCIATED SEVERE APLASTIC-ANEMIA BY IMMUNOSUPPRESSION - A CASE-REPORT AND REVIEW OF THE LITERATURE, Journal of maternal-fetal investigation, 6(3), 1996, pp. 175-178
Severe aplastic anemia (SAA) developing in pregnancy is a serious cond
ition in which therapeutic options like antithymocyte globulin (ATG),
immunosuppression, and bone mat-row transplantation (BMT) must be cons
idered if the fetus is to survive. We consider a case of SAA developin
g in a 27-year-old woman in the 20th week of her third pregnancy is de
scribed. Until delivery at 36 weeks the patient received 48 units of i
rradiated leukocyte-free erythrocytes and 60 units of single-donor pla
telets. At week 36 cesarean hysterectomy was performed, and a healthy
2540-g boy was delivered. BMT could not be performed as no matching do
nor was available. After delivery ATG therapy was started. The patient
remained transfusion-dependent. Leukcocyte count improved after splen
ectomy, and complete remission of SAA with self-sustaining hematopoies
is was observed 19 months after delivery. The patient is in complete h
ematological remission 4 years after ATG treatment. Our report is the
first showing long term survival after SAA developing in pregnancy in
a patient that was not treated with BMT.