Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/2410
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dc.contributor.authorMahesh Karigoudar, Jadhav PT Jadhav PT Rajani Jadhav Kartik Jadhav Akshay Jadhav-
dc.date.accessioned2020-05-28T05:40:10Z-
dc.date.available2020-05-28T05:40:10Z-
dc.date.issued2014-05-
dc.identifier.urihttp://hdl.handle.net/123456789/2410-
dc.description.abstractChorioangioma of placenta is a relatively rare tumor (0.65-1%), most often it goes unnoticed and presents with complications and hence it has potential serious maternal and fetal risk, necessitating close supervision. We present a case, Primigravida, 21 years with 17 weeks of gestation, with large chorioangioma with abruptio placenta and fetal demise.en_US
dc.language.isoenen_US
dc.publisherB.L.D.E.(Deemed to be University)en_US
dc.subjectChorioangioma, Hemartoma, Ultrasound, abruptio placenta.en_US
dc.titleCase of atypical placental large chorioangioma.en_US
dc.typeArticleen_US
Appears in Collections:Faculty of Pathology

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