Atıf İçin Kopyala
BÜYÜKAŞIK Y., Boyraz G., Selcuk I., Bektas Ö., TUNCER Z. S.
ACTA HAEMATOLOGICA, cilt.128, sa.3, ss.154-157, 2012 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
128
Sayı:
3
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Basım Tarihi:
2012
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Doi Numarası:
10.1159/000339085
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Dergi Adı:
ACTA HAEMATOLOGICA
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.154-157
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Anahtar Kelimeler:
Glanzmann's thrombasthenia, Platelet refractoriness, Corpus luteum rupture, Abdominopelvic haematoma, Tranexamic acid, RECOMBINANT FACTOR VIIA, BLEEDING DISORDERS, CORPUS-LUTEUM, WOMEN, HEMORRHAGE, HEMOPERITONEUM, COMPLICATION, MENORRHAGIA
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Karadeniz Teknik Üniversitesi Adresli:
Hayır
Özet
Glanzmann's thrombasthenia (GT) is a very rare autosomal recessive genetic bleeding disorder. Women with coagulation abnormalities are at increased risk of corpus luteum rupture and haemoperitoneum. Here we present a severe case of GT resulting in a haematoma extending from the pelvis to the liver that could only be controlled by surgery and intra-abdominal tranexamic acid. Copyright (c) 2012 S. Karger AG, Basel