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Massive hemoperitoneum due to a ruptured corpus luteum cyst in a patient with congenital hypofibrinogenemia
Article en En | WPRIM | ID: wpr-62645
Biblioteca responsable: WPRO
ABSTRACT
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 ovulation in a woman with congenital afibrogenemia is also a very rare clinical condition. Massive hemoperitoneum usually presents as acute abdominal pain with potential findings of peritonitis including abdominal distention, hypotension and tachycardia with critical consequences. We performed emergent endoscopic surgery for hemoperitoneum caused by a ruptured corpus luteum cyst in a patient with congenital hypofibrinogenemia. To the best of our knowledge, this was the first case report of such treatment in Korea.
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Texto completo: 1 Índice: WPRIM Asunto principal: Quistes Ováricos / Ovulación / Peritonitis / Rotura / Taquicardia / Fibrinógeno / Dolor Abdominal / Incidencia / Cuerpo Lúteo / Afibrinogenemia Tipo de estudio: Incidence_studies / Prognostic_studies Límite: Female / Humans País/Región como asunto: Asia Idioma: En Revista: Obstetrics & Gynecology Science Año: 2015 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Quistes Ováricos / Ovulación / Peritonitis / Rotura / Taquicardia / Fibrinógeno / Dolor Abdominal / Incidencia / Cuerpo Lúteo / Afibrinogenemia Tipo de estudio: Incidence_studies / Prognostic_studies Límite: Female / Humans País/Región como asunto: Asia Idioma: En Revista: Obstetrics & Gynecology Science Año: 2015 Tipo del documento: Article