Severe HPA-15b related neonatal alloimmune thrombocytopenia

The HPA‐15 platelet (PLT) group was recently described. Severe neonatal thrombocytopenia due to alloimmunization by HPA‐15b has very rarely been observed. A 22‐year‐old mother, gravida 1/para 1, gave birth to a male infant who presented with a severe thrombocytopenia, the PLT count recorded to be 3...

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Bibliographic Details
Published in:Acta Paediatrica Vol. 96; no. 11; pp. 1701 - 1703
Main Authors: Moncharmont, P, Courvoisier, S, Pagnier, A, Cotta, L, Debillon, T, Rigal, D
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-11-2007
Blackwell
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Summary:The HPA‐15 platelet (PLT) group was recently described. Severe neonatal thrombocytopenia due to alloimmunization by HPA‐15b has very rarely been observed. A 22‐year‐old mother, gravida 1/para 1, gave birth to a male infant who presented with a severe thrombocytopenia, the PLT count recorded to be 3 ×109/L. A few hours after birth, he developed purpura with extensive haematomas but without visceral or intracranial haemorrhage (ICH). Two PLT transfusions were given including one using maternal PLTs. The infant's PLT count was 267 × 109/L on day 6. The maternal platelet group was HPA‐15a/a and her infant was HPA‐15a/b. Anti‐HPA‐15b antibodies was found in maternal serum. Conclusion: HPA‐15b maternal alloimmunization may induce severe neonatal thrombocytopenia. In order to establish the frequency of neonatal alloimmune thrombocytopenia (NAIT) due to anti‐HPA‐15b antibodies, an improved detection method is necessary.
Bibliography:ark:/67375/WNG-ZKS3HQR5-T
ArticleID:APA483
istex:14E91BD7D0A0DB692E1528838F8C529EB1402053
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0803-5253
1651-2227
DOI:10.1111/j.1651-2227.2007.00483.x