Splenogonadal Fusion in Children: A Rare Entity Mimicking Inguinal Tumor
| dc.contributor.author | Guney, Isa Burak | |
| dc.contributor.author | Temiz, Abdulkerim | |
| dc.contributor.author | Oksuzler, Mahmut | |
| dc.contributor.author | Alkan, Murat | |
| dc.contributor.pubmedID | 32149797 | en_US |
| dc.contributor.researcherID | A-4719-2018 | en_US |
| dc.date.accessioned | 2021-03-31T12:19:22Z | |
| dc.date.available | 2021-03-31T12:19:22Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | Splenogonadal fusion (SGF) is a rare congenital malformation, which can be of a continuous or discontinuous type. It is characterized by splenic tissue fused with gonadal tissue. Because it lacks characteristic features, very few cases of SGF have been diagnosed preoperatively. Herein, we present a case with left side SGF who was diagnosed by Tc-99m-nanocolloid spleen scintigraphy. | en_US |
| dc.identifier.endpage | 454 | en_US |
| dc.identifier.issn | 0363-9762 | en_US |
| dc.identifier.issue | 6 | en_US |
| dc.identifier.scopus | 2-s2.0-85084271780 | en_US |
| dc.identifier.startpage | 453 | en_US |
| dc.identifier.uri | http://hdl.handle.net/11727/5648 | |
| dc.identifier.volume | 45 | en_US |
| dc.identifier.wos | 000538735400024 | en_US |
| dc.language.iso | eng | en_US |
| dc.relation.isversionof | 10.1097/RLU.0000000000002989 | en_US |
| dc.relation.journal | CLINICAL NUCLEAR MEDICINE | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Tc-99m-nanocolloid spleen scintigraphy | en_US |
| dc.subject | magnetic resonance imaging | en_US |
| dc.subject | ultrasonography | en_US |
| dc.subject | splenogonadal fusion | en_US |
| dc.title | Splenogonadal Fusion in Children: A Rare Entity Mimicking Inguinal Tumor | en_US |
| dc.type | Editorial | en_US |
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