{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T08:33:51Z","timestamp":1740126831801,"version":"3.37.3"},"reference-count":30,"publisher":"Georg Thieme Verlag KG","issue":"06","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Z Geburtshilfe Neonatol"],"published-print":{"date-parts":[[2024,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Depending on its location, size, and proximity to the cardiac structures, an\n                    intrapericardial teratoma may lead to severe circulatory disturbances and even\n                    fetal demise. A 34-year-old G2P1 presented at 20w5d with a solid cystic mass in\n                    the right thorax of the fetus, originating from the right atrium or lung, with\n                    signs of non-immune fetal hydrops, soon resulting in intrauterine fetal death.\n                    Detailed post-mortem autopsy revealed signs of hydrops fetalis universalis due\n                    to a spherical tumor mass originating from the aortic root. Histologic\n                    examination of the tumor showed the characteristic morphology of a teratoma. A\n                    1.6-Mb microdeletion at 3q29 was identified by single nucleotide polymorphism\n                    array. This is the first report presenting the diagnosis of an intrapericardial\n                    teratoma in a fetus with a microdeletion of 3q29. Intrapericardial teratoma has\n                    a poor prognosis and the fetal outcome relies on the development of hydrops. A\n                    post-mortem examination is essential in order to make a definitive diagnosis,\n                    which underlines the status of the fetal pathologist and the need for\n                    interdisciplinary cooperation. <\/jats:p>","DOI":"10.1055\/a-2365-8188","type":"journal-article","created":{"date-parts":[[2024,8,22]],"date-time":"2024-08-22T04:46:43Z","timestamp":1724302003000},"page":"528-533","source":"Crossref","is-referenced-by-count":0,"title":["Intrapericardial Teratoma and Associated 3q29 Deletion in a Fetus:\n                    Case Report"],"prefix":"10.1055","volume":"228","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3517-3046","authenticated-orcid":false,"given":"Onur","family":"Guralp","sequence":"additional","affiliation":[{"name":"Division of Prenatal Medicine & Fetal Therapy,\n                    University Hospital for Obstetrics and Gynecology, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katharina","family":"Schoner","sequence":"additional","affiliation":[{"name":"Institute of Pathology, Department of Fetal Pathology,\n                    University Hospital of Giessen and Marburg Campus Marburg, Marburg,\n                    Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aline","family":"Wolter","sequence":"additional","affiliation":[{"name":"Division of Prenatal Medicine & Fetal Therapy,\n                    University Hospital for Obstetrics and Gynecology, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Johanna","family":"Schenk","sequence":"additional","affiliation":[{"name":"Division of Prenatal Medicine & Fetal Therapy,\n                    University Hospital for Obstetrics and Gynecology, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maleen","family":"Reitz","sequence":"additional","affiliation":[{"name":"Division of Prenatal Medicine & Fetal Therapy,\n                    University Hospital for Obstetrics and Gynecology, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ellydda","family":"Widriani","sequence":"additional","affiliation":[{"name":"Division of Prenatal Medicine & Fetal Therapy,\n                    University Hospital for Obstetrics and Gynecology, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katrin","family":"Froebius","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Axel","family":"Weber","sequence":"additional","affiliation":[{"name":"Medizinische Genetik Mainz, Limbach Genetics, Mainz,\n                    Germany"},{"name":"Center for Human Genetics, University of Marburg,\n                    Marburg, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roland","family":"Axt-Fliedner","sequence":"additional","affiliation":[{"name":"Division of Prenatal Medicine & Fetal Therapy,\n                    University Hospital for Obstetrics and Gynecology, University Hospital Giessen\n                    and Marburg Campus Giessen, Giessen, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"194","published-online":{"date-parts":[[2024,8,20]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","first-page":"296","DOI":"10.1002\/uog.5260","article-title":"Spectrum and outcome of prenatally diagnosed fetal 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