Bicorne uterus and renal agenesis associated with preeclampsia.

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Liliana Quisanga
Ruth Montero
David Aulestia
Carlos Vega Cueva

Abstract

Introduction: Renal agenesis originates from defects in embryonic development of Metanefros, is an uncommon entity that has an approximate incidence of 1:1000 births. It is more frequent on the left side and male sex. The Association of congenital defects of mullerianas structures and renal agenesis, is related to hypertensive disorders during pregnancy. The case of a 17-year-old patient with a 25-week pregnancy by ultrasound and 28 weeks per last menstruation date is presented, with a history of bicorn uterus and left renal agenesis, which during his hospitalization was also diagnosed with severe pre-eclampsia.


Objective: To describe a clinical case of extrahepatic cholangiocarcinoma of distal common bile duct.


Material and methods: Retrospective descriptive study, clinical case presentation.


Results: We present the case of a 17-year-old patient with a 25-week pregnancy by ultrasound and 28 weeks on the date of late menstruation unreliable, with a history of bicorne uterus, left renal agenesis, which during his hospitalization is also diagnosed as Severe pre-eclampsia.


Conclusions: The diagnosis of Mullerianas malformations associated with other congenital defects such as renal agenesis, is based on the thorough preparation of the clinical history, which establishes the relationship between the congenital pathologies described and the complications They may present during pregnancy, such as hypertensive disorders (pre-eclampsia). MRI is the most accurate technique, which allows diagnosing and classifying malformations, increasing the diagnostic efficacy. 

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How to Cite
Quisanga, L., Montero, R., Aulestia, D., & Vega Cueva, C. (2018). Bicorne uterus and renal agenesis associated with preeclampsia. Mediciencias UTA, 2(4), 17–20. Retrieved from https://revistas.uta.edu.ec/erevista/index.php/medi/article/view/1228
Section
Clinical case presentation article

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