Abstract |
Glanzmann thrombasthenia (GT) is a rare autosomal recessive disorder which deficiency of the platelet glycoprotein IIb - III a. The disorder usually manifests as severe mucocutaneus bleeding in the chaildhood, menstrual patterns in pubertal--adolescent years, rarely life-threatening. Pregnancy and delivery in patients with TG are very rare and are associated with high risk for mother and fetus due to intra - and post-partum hemorrhage. We present a case 30, a patient with TG, emergency births by caesarean section, with intra- and postpartum haemorrhage managed through the use of recombinant factor VIIa, transfusion of packed red blood cells and platelets.
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Authors | E Uchikova, B Pechlivanov, N Parahuleva, G Amaliev |
Journal | Akusherstvo i ginekologiia
(Akush Ginekol (Sofiia))
Vol. 53
Issue 5
Pg. 49-51
( 2014)
ISSN: 0324-0959 [Print] Bulgaria |
PMID | 25558673
(Publication Type: Case Reports, Journal Article, Review)
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Chemical References |
- Recombinant Proteins
- recombinant FVIIa
- Factor VIIa
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Topics |
- Adult
- Cesarean Section
- Erythrocyte Transfusion
- Factor VIIa
(therapeutic use)
- Female
- Humans
- Platelet Transfusion
- Postpartum Hemorrhage
(therapy)
- Pregnancy
- Pregnancy Complications, Hematologic
(therapy)
- Recombinant Proteins
(therapeutic use)
- Thrombasthenia
(therapy)
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