| Literature DB >> 31331930 |
Michelle Yu1, Kathryn Graham1, Leonardo Pasalic2, Thushari Indika Alahakoon3.
Abstract
Haemolytic disease of the fetus and newborn (HDFN) is associated with red cell antibodies. Anti-M usually results in a mild haemolysis and is rarely clinically significant. There is no established consensus on management of pregnancies with anti-M. A case of recurrent HDFN with maternal M alloimmunisation was identified at a tertiary hospital in Australia. We collected the patient and neonate's clinical and pathological data and interpreted the case with available literature. This is the first case in literature of recurrent fetal hydrops in the setting of M alloimmunisation. Neonate was delivered in a poor condition, intubated and admitted to the neonatal intensive care unit for ionotropic support, red cell transfusion and plasma transfusion for coagulopathy. Direct Coombs test was positive, confirming HDFN. Although anti-M rarely causes HDFN, accurate history, fetal surveillance and monitoring is essential for identification of fetal anaemia. Concurrent placental disease may increase fetal risk from anti-M antibodies. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: haematology (incl blood transfusion); pregnancy
Mesh:
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Year: 2019 PMID: 31331930 PMCID: PMC6664319 DOI: 10.1136/bcr-2019-230552
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X