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https://doi.org/10.1016/j.epsc.2020.101587			18

論文情報

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アクセス権	open access
URI	https://hdl.handle.net/2115/79690
タイトル	Congenital urogenital sinus anomaly in a patient with sacrococcygeal teratoma
著者	Nakamura, Michiko ; Moriya, Kimihiko ; Honda, Shohei ; Ara, Momoko ; Nishimura, Yoko ; Kon, Masafumi ; Chiba, Hiroki ; Kitta, Takeya ; Shinohara, Nobuo
e-Rad_Researcher 60571718 著者名 Nakamura, Michiko
e-Rad_Researcher 20374233 著者名 Moriya, Kimihiko
e-Rad_Researcher 90588089 著者名 Honda, Shohei
e-Rad_Researcher 30741219 著者名 Ara, Momoko
著者名 Nishimura, Yoko
e-Rad_Researcher 40802799 著者名 Kon, Masafumi
著者名 Chiba, Hiroki
e-Rad_Researcher 40374441 著者名 Kitta, Takeya
e-Rad_Researcher 90250422 著者名 Shinohara, Nobuo
言語	英語
キーワード	Sacrococcygeal teratoma
	Urogenital sinus anomaly
	Congenital defect
発行日	2020-10
出版者	Elsevier
収録物名	Journal of Pediatric Surgery Case Reports
巻(号)	61
ページ	101587
抄録	Sacmcoccygeal teratoma (SCT) is the most common fetal and neonatal tumor. While SCT is often associated with urological problems, the association between SCT and a umgenital sinus (UGS) anomaly is rare. A concurrent UGS anomaly may be an acquired condition due to resection of SCT because it is rarely found at birth. In our case in whom fetal imaging study showed an abdominal cystic lesion, SCT with a UGS anomaly was suspected at birth and confirmed by endoscopy before resection of SCT during the neonatal period. These findings revealed that UGS anomaly may develop congenitally.
資源タイプ	学術雑誌論文
出版タイプ	Version of Record
権利情報	Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
PISSN	2213-5766
関連情報 (isIdenticalTo)	出版社版DOI https://doi.org/10.1016/j.epsc.2020.101587

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