Neonatal haemolytic disease with co-existing Anti-D and Anti-C antibodies: an unusual experience

Authors

  • Hafiza Mehreen Durrani Department of Pediatrics, Dr. Ruth KM Pfau Civil Hospital, Karachi, Pakistan
  • Zubia Zaman 4th Year MBBS Student, DOW University of Health Sciences, Karachi, Pakistan https://orcid.org/0000-0002-3015-0160
  • Imran Mansoor Raza 4th Year MBBS Student, DOW University of Health Sciences, Karachi, Pakistan
  • Munira Jamali Dow University of Health Sciences, Karachi, Pakistan
  • Ayesha Saleem Department of Pediatrics, Dr. Ruth KM Pfau Civil Hospital, Karachi, Pakistan
  • Shabana Muzammil Ejaz Department of Pediatrics, Dr. Ruth KM Pfau Civil Hospital, Karachi, Pakistan

DOI:

https://doi.org/10.47391/JPMA.4564

Abstract

Neonatal haemolytic disease in the new-born remains of prime importance for paediatricians due to high perinatal morbidity and mortality rates. The Rh antigen family comprises several different antigens, out of which, D antigen incompatibility is well known for causing severe haemolytic disease in the foetus. Although the current literature shows anomalous cases where coexisting non-D-Rh and D-Rh antigens are the causative agents, there is very little information regarding post-natal outcomes in neonates bearing two different incompatibilities simultaneously. Herein, we discuss an unusual case of anti-D as well as anti-C antibodies (non-D-Rh) in a male neonate born to a Rh-negative mother, who developed jaundice and haemolysis in post-natal life. The neonate underwent exchange transfusion and photo therapy due to raised serum bilirubin levels, supplemented with repeated blood transfusions, intravenous immunoglobulin therapy, and immunosuppressive therapy.

--Continue

Published

2022-10-15

How to Cite

Durrani, H. M., Zaman, Z., Mansoor Raza, I., Jamali, M., Saleem, A., & Muzammil Ejaz, S. (2022). Neonatal haemolytic disease with co-existing Anti-D and Anti-C antibodies: an unusual experience. Journal of the Pakistan Medical Association, 72(11), 2320–2322. https://doi.org/10.47391/JPMA.4564

Issue

Section

CASE REPORT