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CASE REPORT
Bilateral cystic encephalomalacia following multiple intrauterine transfusions for anti-Kell isoimmunisation
  1. Hesham Elsayed1,
  2. Mansum Ng2,
  3. Mary Rutherford3,
  4. Rajesh Gupta4
  1. 1Department of Paediatrics, Barts Health, London, UK
  2. 2Department of Paediatrics, Tunbridge Wells Hospital, Tunbridge Wells, UK
  3. 3Centre for the Developing Brain, King's College London, London, UK
  4. 4Department of Paediatrics and Neonates, Tunbridge Wells Hospital, Tunbridge Wells, UK
  1. Correspondence to Dr Rajesh Gupta, r.gupta{at}nhs.net

Summary

Fetal and neonatal haemolytic diseases result from maternal allo-immunisation to fetal antigens. Maternal antibodies cross the placenta causing red cell haemolysis, resulting in fetal anaemia and, in severe cases, hydrops and perinatal death. Intravascular intrauterine blood transfusion (IUT) has markedly reduced perinatal mortality and is now a standard procedure. IUT is considered to be a safe procedure with fetal loss rate reported to be less than 5% and no reported increase in the rate of neurodevelopment impairment. In this report, we are presenting a case of bilateral cystic encephalomalacia following fetal anaemia secondary to anti-Kell iso-immunisation treated with multiple IUTs. Such a significant adverse outcome following IUT for anti-Kell iso-immunisation has not been reported in the literature. This case highlights the need for appropriate parental counselling and routine postnatal head ultrasound in all babies delivered following multiple IUTs.

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