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Spontaneous Rupture of Internal Iliac Artery in Pregnancy: Case Report
- Source :
- Acta Clinica Croatica, Vol 57., Iss 1., Pp 157-160 (2018)
- Publication Year :
- 2018
- Publisher :
- Sestre Milosrdnice University hospital, Institute of Clinical Medical Research, 2018.
-
Abstract
- Rupture of the internal iliac artery is a rare complication in pregnancy that is associated with maternal and fetal morbidity and mortality. We present a case of a 30-year-old primipara admitted to our department in 39th week of gestation after sudden onset of intense abdominal pain. On admission, the patient was pale, tachycardiac, but with normal blood pressure and afebrile. Symptoms of acute abdomen were clear and surgery was indicated. Diagnosis was confirmed during cesarean section. Enlarged gravid uterus compressed the ruptured artery and prevented heavier bleeding. Acute bleeding due to arterial rupture causes severe symptoms, predominantly abdominal pain. Changes in blood count become significant some time after the onset of rupture. As the gravid uterus compressed the arterial rupture, preoperative bleeding was by far less abundant than the bleeding after the baby had been delivered and the size of the uterus decreased. Any cause of acute abdomen during pregnancy (abruption of the placenta, spleen rupture, visceral artery thrombosis) requires urgent surgical treatment, as well as intraoperative and postoperative intensive treatment. Rupture of the internal iliac artery is a rare complication in pregnancy, but has to be considered as a differential diagnosis of abdominal pain.
- Subjects :
- Iliac artery
Pregnancy
Abdominal pain
Abdomen, acute
Cesarean section
Medicine
Subjects
Details
- Language :
- English
- ISSN :
- 03539466 and 13339451
- Volume :
- 57.
- Issue :
- 1.
- Database :
- Directory of Open Access Journals
- Journal :
- Acta Clinica Croatica
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.7c4fdfb0147d40eaa8cbcee923f0c521
- Document Type :
- article
- Full Text :
- https://doi.org/10.20471/acc.2018.57.01.20