Transient aplastic crisis triggered by parvovirus B19 in a family with hereditary spherocytosis
Nicolas Cilla,
Léa Domitien,
Neila Arrada,
Delphine Chiffre,
Perrine Mahe,
Laure Vincent,
Patricia Aguilar-Martinez,
Vincent Foulongne
Affiliations
Nicolas Cilla
Department of Clinical Hematology, Montpellier University Hospital, 34295, Montpellier, France
Léa Domitien
Division of Hematologic Diseases, Department of Pediatrics, Montpellier University Hospital, University Montpellier, Montpellier, France
Neila Arrada
Pathogenesis and Control of Chronic Infections, University of Montpellier, INSERM, EFS, Montpellier University Medical Centre, 34090, Montpellier, France
Delphine Chiffre
Department of Biological Hematology, Montpellier University Medical Centre & University of Montpellier, Montpellier, France
Perrine Mahe
Division of Hematologic Diseases, Department of Pediatrics, Montpellier University Hospital, University Montpellier, Montpellier, France; Reference Center on Rare Red Cell Disorders, Montpellier University Medical Centre, Montpellier, France
Laure Vincent
Department of Clinical Hematology, Montpellier University Hospital, 34295, Montpellier, France
Patricia Aguilar-Martinez
Department of Biological Hematology, Montpellier University Medical Centre & University of Montpellier, Montpellier, France; Reference Center on Rare Red Cell Disorders, Montpellier University Medical Centre, Montpellier, France
Vincent Foulongne
Pathogenesis and Control of Chronic Infections, University of Montpellier, INSERM, EFS, Montpellier University Medical Centre, 34090, Montpellier, France; Corresponding author at: Virology department, Centre Hospitalier Regional Universitaire de Montpellier, 80, Avenue Augustin Fliche, 34295, Montpellier Cedex 5, France.
Acute parvovirus B19 infection may lead to erythroblastopenia crisis in patients with underlying red blood cells disorders. We report herein an uncommon concomitant transient aplastic crisis in a mother and her daughter, both affected by hereditary spherocytosis. The diagnosis was confirmed by the detection of a very high parvovirus B19 DNA load in both the mother’s and daughter’s sera, associated with the presence of parvovirus B19 specific immunoglobulin-M antibodies. This rapid etiologic diagnosis allowed to save bone marrow sampling, although blood transfusion was required regarding the severe anemia associated with pancytopenia. Our observation illustrates first line parvovirus B19 hypothesis in the context of transient aplastic crisis and that contagiousness in household contacts should be considered in family with a medical history of red blood cell pathology.