| Literature DB >> 12070051 |
Angel F Remacha1, Isabel Badell, Núria Pujol-Moix, Juan Parra, Eduardo Muñiz-Diaz, Gemma Ginovart, M Pilar Sardà, Angel Hernández, Elisenda Moliner, Montserrat Torrent.
Abstract
Hydrops fetalis is rarely caused by congenital dyserythropoietic anemia (CDA). We report a patient with hydrops fetalis as a result of severe anemia. This patient needed intrauterine transfusions from 21 weeks of gestation until birth. The hematologic study showed an atypical CDA (hydrops fetalis-associated CDA) characterized by features resembling CDA type II, but negative acidified serum lysis test (HEMPAS negative). The patient was regularly transfused for a year, after which an allogeneic bone marrow transplantation (BMT) from an HLA-identical sibling was successfully carried out. His actual hemoglobin is 127 g/L, and he has not received transfusions for more than a year. In conclusion, intrauterine transfusions and BMT could cure an otherwise lethal atypical CDA.Entities:
Mesh:
Year: 2002 PMID: 12070051 DOI: 10.1182/blood-2001-12-0351
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113