Case report: a pregnant woman with immune thrombocytopenic purpura and unusual red cell antibodies
, , oraz
17 lis 2020
O artykule
Data publikacji: 17 lis 2020
Zakres stron: 153 - 155
DOI: https://doi.org/10.21307/immunohematology-2019-808
Słowa kluczowe
© 1995 C.R. Nanton published by Sciendo
Maternal immune thrombocytopenic purpura (ITP) may lead to fetal platelet destruction. This process is mediated by IgG platelet autoantibodies that cross the placenta. In this case, not only were platelet autoantibodies present, but red cell alloantibodies anti-E, anti-M, and anti-He were also present. Anti-E, present as an IgG antibody, crossed the placenta, but did not cause clinical problems in the E+ newborn, other than possible hyperbilirubinemia that was treated by phototherapy.