Successful management of a hydropic fetus with severe anemia and thrombocytopenia caused by anti-CD36 antibody

Successful management of a hydropic fetus with severe anemia and thrombocytopenia caused by anti-CD36 antibody
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DOI:
10.1007/s12185-017-2310-5
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发表时间:
2018-02-01
影响因子:
2.1
通讯作者:
Fang, Qun
Fang, Qun
中科院分区:
医学4区
文献类型:
--
作者:
Xu, Xiuzhang;Li, Lin;Fang, Qun

文献摘要

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Cases of CD36 deficiency are not rare in Asian populations, foetal and neonatal alloimmune thrombocytopenia (FNAIT) caused by anti-CD36 isoantibodies appears more frequent than other HPA alloantibodies. However, little is known about the treatment of anti-CD36 mediated FNAIT in this region. A Chinese male foetus, whose mother had a history of multiple intrauterine foetal demise and/or hydrops, was diagnosed with severe FNAIT at 27 weeks of gestational age. Immunological analysis revealed total absence of CD36 on platelets and monocytes from mother, caused by a 329-330delAC mutation of the CD36 gene. Anti-CD36 and anti-HLA class I antibodies were detected in the maternal serum, whereas only anti-CD36 isoantibodies were detectable in the foetal blood sample. Serial intrauterine transfusions with red blood cells (RBC) and platelets from a CD36null donor were performed to improve the severe anaemia and thrombocytopenia. The baby (2250 g; Apgar scores 10) was delivered vaginally at 32 weeks of gestation with normal haemoglobin (186 g/L) but low platelet count (48 x 10(9)/L). After 2 days the platelet count rose to 121 x 10(9)/L. This report suggests that intrauterine transfusions with compatible RBC and CD36null platelets are useful in preventing the deleterious clinical effects of anti-CD36-mediated severe FNAIT.