Postpartum Acquired Hemophilia : A Rare Cause of Postpartum Hemorrhage

المؤلفون المشاركون

Seethala, Srikanth
Gaur, Sumit
Enderton, Elizabeth
Corral, Javier

المصدر

Case Reports in Hematology

العدد

المجلد 2013، العدد 2013 (31 ديسمبر/كانون الأول 2013)، ص ص. 1-2، 2ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2013-02-28

دولة النشر

مصر

عدد الصفحات

2

التخصصات الرئيسية

الأمراض

الملخص EN

A 36-year-old female started having postpartum vaginal bleeding after normal vaginal delivery.

She underwent hysterectomy for persistent bleeding and was referred to our institution.

An elevation of PTT and normal PT made us suspect postpartum acquired hemophilia (PAH), and it was confirmed by low factor VIII activity levels and an elevated factor VIII inhibitor.

Hemostasis was achieved with recombinant factor VII concentrates and desmopressin, and factor eradication was achieved with cytoxan, methylprednisolone, and plasmapheresis.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Seethala, Srikanth& Gaur, Sumit& Enderton, Elizabeth& Corral, Javier. 2013. Postpartum Acquired Hemophilia : A Rare Cause of Postpartum Hemorrhage. Case Reports in Hematology،Vol. 2013, no. 2013, pp.1-2.
https://search.emarefa.net/detail/BIM-494525

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Seethala, Srikanth…[et al.]. Postpartum Acquired Hemophilia : A Rare Cause of Postpartum Hemorrhage. Case Reports in Hematology No. 2013 (2013), pp.1-2.
https://search.emarefa.net/detail/BIM-494525

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Seethala, Srikanth& Gaur, Sumit& Enderton, Elizabeth& Corral, Javier. Postpartum Acquired Hemophilia : A Rare Cause of Postpartum Hemorrhage. Case Reports in Hematology. 2013. Vol. 2013, no. 2013, pp.1-2.
https://search.emarefa.net/detail/BIM-494525

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-494525