Massive hemoperitoneum due to a ruptured corpus luteum cyst in a patient with congenital hypofibrinogenemia

Congenital afibrinogenemia/hypofibrinogenemia is a rare inherited hematologic disorder in which a patient lacks or has insufficient level of fibrinogen, the blood coagulation factor I. The incidence of this uncommon disease is 1 to 2 per 1 million individuals. Hence, massive hemoperitoneum caused by...

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Detalles Bibliográficos
Autores principales: Kim, Jong-Hyun, Jeong, So-Young, Cho, Dong-Hyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Obstetrics and Gynecology; Korean Society of Contraception and Reproductive Health; Korean Society of Gynecologic Endocrinology; Korean Society of Gynecologic Endoscopy and Minimal Invasive Surgery; Korean Society of Maternal Fetal Medicine; Korean Society of Ultrasound in Obstetrics and Gynecology; Korean Urogynecologic Society 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588852/
https://www.ncbi.nlm.nih.gov/pubmed/26430672
http://dx.doi.org/10.5468/ogs.2015.58.5.427

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588852/
https://www.ncbi.nlm.nih.gov/pubmed/26430672
http://dx.doi.org/10.5468/ogs.2015.58.5.427

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