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dc.contributor.authorPulei, AN
dc.contributor.authorMuga, PA
dc.contributor.authorOngeti, KW
dc.contributor.authorKinuthia, J
dc.contributor.authorOgutu, O
dc.date.accessioned2017-05-02T07:43:04Z
dc.date.available2017-05-02T07:43:04Z
dc.date.issued2017
dc.identifier.citationPulei, A. N., et al. "Unilateral spontaneous tubal twin ectopic pregnancy: A rare occurrence." Anatomy Journal of Africa 6.1 (2017): 819-823.en_US
dc.identifier.urihttps://www.ajol.info/index.php/aja/article/view/150683
dc.identifier.urihttp://hdl.handle.net/11295/100778
dc.description.abstractUnilateral tubal twin pregnancy remains rare despite a rise in the incidence of singleton ectopic pregnancies. A 27-year-old Gravida 1 Para 0+0 at 12 weeks gestation, presented to our institution with a 1-month history of lower abdominal pain, that progressively worsened and became very severe. An abdominal ultrasound revealed an extrauterine gestational sac that looked like a single viable fetus in the right adnexa at about 12 weeks by crown rump length. Free fluid was noted in the right iliac fossa and Morrison’s pouch. A conclusion of a right-ruptured ectopic pregnancy was made. The patient underwent laparotomy and a diagnosis of twin right-sided fimbrial ectopic pregnancy was made. The crown rump lengths of the twins were 6cm and 4cm. We present this case because unilateral tubal twin pregnancy is still a rare phenomenon, and clinicians as well as clinical embryologists need to acknowledge its existence considering the diagnosis of this case was not made pre-operatively.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectTwin Tubal, ectopic pregnancy, unilateralen_US
dc.titleUnilateral spontaneous tubal twin ectopic pregnancy: a rare occurrenceen_US
dc.typeArticleen_US


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States