| Literature DB >> 33569741 |
Eriko Shima1, Hayato Go1, Hajime Maeda2, Kei Ogasawara1, Takashi Imamura1,3, Mutsumi Sasaki4, Yangsook Koh5, Kenneth E Nollet4, Kazuhiko Ikeda4, Hitoshi Ohto6, Mitsuaki Hosoya1.
Abstract
Neonatal alloimmune thrombocytopenia (NAIT) arises from fetomaternal platelet incompatibility that results in transplacental passage of maternal antibodies mostly against fetal human platelet antigens (HPA), whereas NAIT due to anti-human leukocyte antigen (HLA) antibodies is extremely rare. Here, we report a case of Down syndrome (DS) with NAIT that was attributed to HLA antibodies. A boy with DS was delivered at 36 weeks' gestation. His platelet count declined to 13.0 × 109/L, suggestive of NAIT rather than other conditions, including transient abnormal myelopoiesis. Random platelet concentrates and intravenous immunoglobulin administration resolved the thrombocytopenia without clinical complications. Immunoserological investigations detected anti-HLA, but no anti-HPA antibodies in samples from the patient and the mother. HLA typing and cross-matching indicated that anti-HLA antibodies to paternal HLA A31 and B61, which had probably been induced during a prior pregnancy, led to NAIT in this case. Although it is a rare condition, healthcare providers should consider NAIT due to HLA antibodies and be vigilant for subsequent cases in DS.Entities:
Keywords: Down syndrome; Human leukocyte antigen; Human platelet antigen; Neonatal alloimmune thrombocytopenia
Year: 2021 PMID: 33569741 DOI: 10.1007/s12185-021-03092-z
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490