Ruptured Rudimentary Uterine Horn Pregnancy: A Case Report
DOI:
https://doi.org/10.52981/sjms.v16i1.1099الكلمات المفتاحية:
rudimentary uterine horn pregnancy، ectopic pregnancy، Mullerian anomalies، early pregnancy complicationالملخص
Pregnancy in rudimentary uterine horn has been reported to be very rare in literature, and is associated with adverse complications. Furthermore, it is also difficult to diagnose, and in most cases, is diagnosed after being ruptured. A case of ruptured rudimentary uterine horn pregnancy presented at Elsaudi Maternity Hospital (Sudan). Despite her recurrent presentation for persistent suprapubic pain and frequent ultrasound scans, the uterine horn pregnancy was not detected, and the diagnosis was made during laparotomy as her condition started to deteriorate progressively due to massive internal bleeding from the ruptured uterine horn
المراجع
[1] Buntugu. K., Ntumy, M., Ameh, E., et al. (2008). Rudimentary horn pregnancy: prerupturediagnosis and management. Ghana Medical Journal, vol. 42, no. 2, pp.92–94.
[2] Chan, Y. Y., Jayaprakasan, K., Zamora, J., et al. (2011). The prevalence of congenitaluterine anomalies in unselected and high-risk populations: a systematic review.Human Reproduction Update, vol. 17, no. 6, pp. 761–771.
[3] Dhar, H. (2012). Ruptured rudimentary horn at 22 weeks. Nigerian Medical Journal,vol. 53, no. 3, pp. 175–177
[4] Ambusaidi, Q. and Jha, C. (2014). Pregnancy in the rudimentary uterine horn: casereport of an unusual presentation. Sultan Qaboos University Medical Journal, vol.14, no. 1, pp. e134–e138.
[5] Jain, R., Gami, N., Puri, M., et al. (2010). A rare case of intact rudimentaryhorn pregnancy presenting as hemoperitoneum. Journal of Human ReproductiveSciences, vol. 3, no. 2, pp. 113–115.
[6] Park, J. K. and Dominguez, C. E. (2007). Combined medical and surgical managementof rudimentary uterine horn pregnancy. JSLS, vol. 11, no. 1, pp. 119–122.
[7] Li, X., Peng, P., Liu, X., et al. (2019). The pregnancy outcomes of patients withrudimentary uterine horn: a 30-year experience. PLoS ONE, vol. 14, no. 1, p.e0210788
[2] Chan, Y. Y., Jayaprakasan, K., Zamora, J., et al. (2011). The prevalence of congenitaluterine anomalies in unselected and high-risk populations: a systematic review.Human Reproduction Update, vol. 17, no. 6, pp. 761–771.
[3] Dhar, H. (2012). Ruptured rudimentary horn at 22 weeks. Nigerian Medical Journal,vol. 53, no. 3, pp. 175–177
[4] Ambusaidi, Q. and Jha, C. (2014). Pregnancy in the rudimentary uterine horn: casereport of an unusual presentation. Sultan Qaboos University Medical Journal, vol.14, no. 1, pp. e134–e138.
[5] Jain, R., Gami, N., Puri, M., et al. (2010). A rare case of intact rudimentaryhorn pregnancy presenting as hemoperitoneum. Journal of Human ReproductiveSciences, vol. 3, no. 2, pp. 113–115.
[6] Park, J. K. and Dominguez, C. E. (2007). Combined medical and surgical managementof rudimentary uterine horn pregnancy. JSLS, vol. 11, no. 1, pp. 119–122.
[7] Li, X., Peng, P., Liu, X., et al. (2019). The pregnancy outcomes of patients withrudimentary uterine horn: a 30-year experience. PLoS ONE, vol. 14, no. 1, p.e0210788
التنزيلات
منشور
2021-08-21
إصدار
القسم
Original Articles
