Copy For Citation
BÜYÜKAŞIK Y., Boyraz G., Selcuk I., Bektas Ö., TUNCER Z. S.
ACTA HAEMATOLOGICA, vol.128, no.3, pp.154-157, 2012 (SCI-Expanded)
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Publication Type:
Article / Article
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Volume:
128
Issue:
3
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Publication Date:
2012
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Doi Number:
10.1159/000339085
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Journal Name:
ACTA HAEMATOLOGICA
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Journal Indexes:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Page Numbers:
pp.154-157
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Keywords:
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 Technical University Affiliated:
No
Abstract
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