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Fetal intracranial hemorrhage related to maternal autoimmune thrombocytopenic purpura
Authors:Mehmet Serdar Kutuk  Laure Croisille  Sureyya Burcu Gorkem  Ebru Yilmaz  Levent Korkmaz  Philippe Bierling  Ekrem Unal
Affiliation:1. Division of Perinatalogy, Faculty of Medicine, Department of Obstetrics and Gynecology, Erciyes University, Kayseri, Turkey
2. Etablissement Francais du Sang (EFS-Ile –de-France), Hopital Henri Mondor, Inserm U955, Creteil, France
3. Faculty of Medicine, Department of Radiology, Division of Pediatric Radiology, Erciyes University, Kayseri, Turkey
4. Faculty of Medicine Department of Pediatrics, Division of Pediatric Hematology and Oncology, Erciyes University, Kayseri, Turkey
5. Faculty of Medicine, Department of Pediatrics, Division of Neonatology, Erciyes University, Kayseri, Turkey
Abstract:

Background

Maternal autoimmune thrombocytopenic purpura (AITP) can cause fetal intracranial hemorrhage.

Case report

A 19-year-old primigravida was referred to our institution for prenatally detected ventriculomegaly at 30th week of gestation. Her personal and family histories were unremarkable. Her platelet count was 54?×?109/L. Fetal neurosonography showed intraparenchymal hemorrhage. AITP was diagnosed in the mother and platelet count decreased at 34?×?109/L. Patient was treated with methylprednisolone and intravenous immunoglobulin. She delivered a 2,340-g infant at 37 weeks with elective cesarean section. The platelet count of the newborn was 181?×?109/L and coagulation tests were normal. No antiplatelet specific antibodies were detected in cord blood. Postnatal MRI evaluation confirmed grade IV intracranial hemorrhage. The newborn baby has suffered from mild spasticity and seizures.

Conclusions

Clinicians must be vigilant about the catastrophic fetal complications of maternal AITP; a close follow-up with a multidisciplinary cooperation between obstetricians, hematologists, and neonatologists must be warranted.
Keywords:
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