Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/111354
Campo DC Valoridioma
dc.contributor.authorBarber, Miguel A.en_US
dc.contributor.authorEguiluz, Idoyaen_US
dc.contributor.authorPlasencia, Walteren_US
dc.contributor.authorMedina Castellano, Margarita Jesúsen_US
dc.contributor.authorValle Morales, Leonoren_US
dc.date.accessioned2021-08-04T08:22:09Z-
dc.date.available2021-08-04T08:22:09Z-
dc.date.issued2009en_US
dc.identifier.issn0020-7292en_US
dc.identifier.urihttp://hdl.handle.net/10553/111354-
dc.description.abstractVarious pathologies may trigger cerebral hemorrhage during the fetal period. Intracranial hemorrhages (ICH) are very rare occurrences and intracranial papilloma can be a cause of ICH. This case concerns a 34-year-old healthy pregnant woman who had no significant medical history and whose initial ultrasound exams revealed normal fetal anatomy and growth. An ultrasound scan at 36 weeks revealed a 35×22 mm tumor in the interior of the right posterior horn (Fig. 1). The tumor was hyperechogenic with an irregular surface and perilesional vascularization. No obstruction to the ventricular system was found. The peak flow speed from the medium cerebral artery was 1.5 MoM for the age of gestation. A diagnosis of an intraventricular tumor was made, compatible with choroid plexus papilloma. Consensus was reached to end gestation via cesarean delivery to prevent a secondary hemorrhage during natural childbirth. At 37 weeks of pregnancy a male neonate was delivered weighing 2885 g, with an Apgar score of 9/10 and an arterial pH of 7.29. The newborn was admitted to the neonatal intensive care unit where cranial MRI and cranial ultrasound were carried out. This revealed a large mass in the right lateral ventricle and associated cysts that had displaced the cerebral parenchyma to the frontal region (Figs. 2 and 3). Cerebral arteriography was carried out, followed by embolization and a right temporal craniotomy and complete removal of the mass. The infant currently has normal neurologic development and is progressing well. ICH is observed in utero as hyperechogenic cerebral images on ultrasound [1]. It is usually associated with various maternal medical histories such as thrombocytopenia, hemorrhagic diathesis, or hypertension in pregnancy [2]. ICH caused by a choroid plexus papilloma is rare [2,3]. Diagnosis is made during ultrasound examinations and various manifestations can be identified, such as encephalic parenchyma, hyperechogenic lesions, ventriculomegaly, and periventricular leucomalacia, which may lead to development of severe hydrocephalus and seriously impact neurological development [1,2,4]. This wide range of ultrasoundmanifestations of the damage caused by ICH is an indication of the number of possible prognoses. Nuclear magnetic resonance imaging is the next step in diagnosing these lesions. In cases of ICH, the intensity of the image in T1 is increased compared with the healthy brain tissue, which can contribute to the diagnosis [1].en_US
dc.languageengen_US
dc.relation.ispartofInternational Journal of Gynecology and Obstetricsen_US
dc.sourceInternational Journal of Gynecology and Obstetrics [ISSN 0020-7292], v. 105(2), p. 172-173en_US
dc.subject32 Ciencias médicasen_US
dc.subject320108 Ginecologíaen_US
dc.subject.otherChoroid plexus papillomaen_US
dc.subject.otherFetal tumoren_US
dc.subject.otherIntracranial fetal hemorrhageen_US
dc.titleIntracranial fetal hemorrhage due to choroid plexus papillomaen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typearticleen_US
dc.identifier.doi10.1016/j.ijgo.2008.11.041en_US
dc.identifier.pmid19200541-
dc.identifier.scopus2-s2.0-64049117541-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.description.lastpage173en_US
dc.identifier.issue2-
dc.description.firstpage172en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages2en_US
dc.utils.revisionen_US
dc.date.coverdateMayo 2009en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr1,408
dc.description.jcrqQ3
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0003-4483-3576-
crisitem.author.fullNameMedina Castellano, Margarita Jesús-
crisitem.author.fullNameValle Morales, Leonor-
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