A rare pediatric case with radiological findings: pelvic cystic schwannoma

dc.contributor.authorKarabulut, Ahmat Kasım
dc.contributor.authorKoc, Gonca
dc.contributor.authorDivarcı, Emre
dc.contributor.authorNaghiyev, Javid
dc.contributor.authorSavas, Recep
dc.date.accessioned2023-01-12T20:37:43Z
dc.date.available2023-01-12T20:37:43Z
dc.date.issued2021
dc.departmentN/A/Departmenten_US
dc.description.abstractSchwannomas are peripheral nerve sheath tumors usually detected in adults which are extremely rare in pediatric population and when present they are commonly associated with Neurofibromatosis type 2. While frequently observed in the head, neck, and extremities, they could be detected anywhere in the body including abdominal cavity. The most common site for intraabdominal schwannomas is stomach and pelvic schwannomas are extremely rare. The imaging characteristics are quite diverse, and they could seldom be pure cystic. Herein, we describe a case in the pediatric age group diagnosed with pelvic cystic schwannoma.en_US
dc.identifier.endpage429en_US
dc.identifier.issn1016-9113
dc.identifier.issn2147-6500
dc.identifier.issue4en_US
dc.identifier.startpage427en_US
dc.identifier.trdizinid1118827en_US
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/1118827
dc.identifier.urihttps://hdl.handle.net/11454/81748
dc.identifier.volume60en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofEge Tıp Dergisien_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleA rare pediatric case with radiological findings: pelvic cystic schwannomaen_US
dc.typeOtheren_US

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