Ultrasound diagnosis of acrania with major low–lying placenta and polyhydramnios; case report

dc.contributor.authorOblitey, J.N.
dc.contributor.authorAntwi, W.K.
dc.contributor.authorBotwe, B.O.
dc.contributor.authorOblitey, M.K.
dc.date.accessioned2021-12-14T12:30:39Z
dc.date.available2021-12-14T12:30:39Z
dc.date.issued2021
dc.descriptionResearch Articleen_US
dc.description.abstractAcrania is a rare foetal anomaly in which the calvaria is absent, and the meninges come into direct contact with the amniotic fluid. Acrania is the most common anomaly in the acrania – exencephaly – anencephaly spectrum, with an incidence of 3.68 to 5.4 per 10,000 live births. We present a case of a primigravida who presented for an ultrasound on account of vaginal bleeding in early cyesis. Transabdominal ultrasound showed a viable foetus at 13 weeks without a calvaria, with the brain in direct contact with amniotic fluid. There was a low-lying placenta extending from the posterior to anterior part of the lower uterine segment, completely covering the internal cervical os (major low–lying placenta), a placental cyst and polyhydramnios (amniotic fluid index, AFI of 17 cm). A diagnosis of acrania with major low–lying placenta and polyhydramnios was made. Detailed ultrasound is required to detect acrania at 13 weeks. The diagnosis of acrania is required to help direct patient counselling and maternal expectation. When acrania and major low–lying placenta occur in the same patient, both diagnoses must be promptly made concurrently, regardless of gestational age and without waiting for placental trophotropism and migration to occur first.en_US
dc.identifier.otherdoi: http://dx.doi.org/10.4314/gmj.v55i2.12
dc.identifier.urihttp://ugspace.ug.edu.gh/handle/123456789/37273
dc.language.isoen_USen_US
dc.publisherGhana Med Jen_US
dc.subjectAcraniaen_US
dc.subjectexencephalyen_US
dc.subjectanencephalyen_US
dc.subjectmajor low-lying placentaen_US
dc.subjectplacental cysten_US
dc.titleUltrasound diagnosis of acrania with major low–lying placenta and polyhydramnios; case reporten_US
dc.typeArticleen_US

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