J. Wicki et al., PAROVIRUS B19-INDUCED RED-CELL APLASIA IN SOLID-ORGAN TRANSPLANT RECIPIENTS - 2 CASE-REPORTS AND REVIEW OF THE LITERATURE, HEM CELL TH, 39(4), 1997, pp. 199-204
Two solid-organ transplant recipients (one heart and one lung) develop
ed severe anemia with reticulocytopenia. Both were heavily immunosuppr
essed. Bone marrow aspiration revealed almost complete absence of eryt
hroid precursors. A few giant megaloblastic proerythroblasts with cyto
plasmic vacuolisation and intranuclear inclusions were seen. Human par
vovirus B19 (B19V)-DNA genome was found by nested-PCR assays in blood
and bone marrow samples in both cases. Twelve similar cases are descri
bed in the literature. When looked for, B19V DNA was positive either i
n serum or bone marrow or both. Twelve of the fourteen patients were s
uccessfully treated by high dose i.v. immunoglobulin (IVIG). One patie
nt recovered spontaneously and another after treatment with recombinan
t human erythropoietin (rHu-EPO) only. Transplant patients should be c
onsidered at risk for severe erythroblastopenic anemia due to B19V inf
ection. Diagnosis is based on bone marrow examination and detection of
B19V DNA by PCR in serum and/or marrow. IVIG is an effective and safe
treatment. The role of erythropoietin in this indication needs furthe
r study.