H. Hasle et al., CHRONIC PARVOVIRUS INFECTION MIMICKING MYELODYSPLASTIC SYNDROME IN A CHILD WITH SUBCLINICAL IMMUNODEFICIENCY, The American journal of pediatric hematology/oncology, 16(4), 1994, pp. 329-333
Purpose: We present a report of a child with subclinical immunodeficie
ncy who became chronically infected with parvovirus resulting in pancy
topenia and morphologic abnormalities in the bone marrow mimicking mye
lodysplastic syndrome (MDS). Patient: An 8-year-old boy presented with
severe anemia, moderate thrombocytopenia and granulocytopenia. The pa
tient showed hyper-immunoglobulin M (IgM) immunedeficiency but no incr
eased susceptibility to infections. The bone marrow was hypercellular
with dysplastic granulocytopoiesis and erythroblastopenia. Results: Tr
eatment with cyclosporine and i.v. Ig resulted in temporary normalizat
ion of the hemoglobin level. For several years it was assumed that the
patient had MDS, A diagnosis of parvovirus infection was initially re
jected due to the lack of specific antibodies and the absence of giant
pronormoblasts in the bone marrow. When the polymerase chain reaction
technique became available, parvovirus DNA was detected from the enti
re disease course. Conclusions: This case report expands our conceptio
n of the clinical spectrum of parvovirus infection and emphasizes that
parvovirus must be considered as a differential diagnosis in MDS. We
recommend performing a parvovirus DNA test despite negative serologic
findings in patients with MDS, especially when associated with immunol
ogic abnormalities.