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Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case
http://hdl.handle.net/20.500.12000/0002020854
http://hdl.handle.net/20.500.12000/00020208546dfeac90-6fae-4c46-81bd-d7e86bd81b1e
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
K_No9p1_2023.pdf (1.1 MB)
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| Item type | 琉球大学リポジトリ登録用アイテムタイプ(1) | |||||||||||||||
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| 公開日 | 2024-11-28 | |||||||||||||||
| タイトル | ||||||||||||||||
| タイトル | Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case | |||||||||||||||
| 言語 | en | |||||||||||||||
| 作成者 |
Kobayashi, Haruka
× Kobayashi, Haruka
× Baba, Tokuro
× Kuda, Masaaki
× Ieiri, Satoshi
× Takatsuki, Mitsuhisa
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| アクセス権 | ||||||||||||||||
| アクセス権 | open access | |||||||||||||||
| アクセス権URI | http://purl.org/coar/access_right/c_abf2 | |||||||||||||||
| 権利情報 | ||||||||||||||||
| 言語 | en | |||||||||||||||
| 権利情報 | © The Author(s) 2023. | |||||||||||||||
| 権利情報 | ||||||||||||||||
| 言語 | en | |||||||||||||||
| 権利情報Resource | http://creativecommons.org/licenses/by/4.0/ | |||||||||||||||
| 権利情報 | This article is licensed under a Creative Commons Attribution 4.0 International License. | |||||||||||||||
| 主題 | ||||||||||||||||
| 言語 | en | |||||||||||||||
| 主題Scheme | Other | |||||||||||||||
| 主題 | Omphalocele | |||||||||||||||
| 主題 | ||||||||||||||||
| 言語 | en | |||||||||||||||
| 主題Scheme | Other | |||||||||||||||
| 主題 | Umbilical evagination of the bladder | |||||||||||||||
| 主題 | ||||||||||||||||
| 言語 | en | |||||||||||||||
| 主題Scheme | Other | |||||||||||||||
| 主題 | Urachal aplasia | |||||||||||||||
| 内容記述 | ||||||||||||||||
| 内容記述タイプ | Other | |||||||||||||||
| 内容記述 | Background A few cases of small omphalocele with umbilical evagination of the bladder have been reported. However, its embryology is yet to be elucidated. Only a few reports have indicated the existence of urachal anomalies and umbilical cysts related to bladder evagination. The incidence of urachal anomalies at birth is reported to be 1 in 5000–8000 live birth, and urachal aplasia is rare. Herein, we report a rare, novel case of urachal aplasia. Case presentation We encountered a small omphalocele with bladder evagination associated with urachal aplasia for which the neonate underwent surgery one day after birth. The patient was a one-day-old boy with a prenatally diagnosed omphalocele. A fetal magnetic resonance image (MRI) scan (25 weeks of gestation) revealed a 30 × 33 mm (approximately 1.3 in.) cystic lesion which was suspected to be an umbilical cyst. The baby was born vaginally at 38 weeks, weighing 2956 g. An omphalocele (hernial orifice diameter, 4 cm × 3 cm) with bladder prolapse was recognized. After sac excision, the prolapsed bladder was resected and closed with two-layer sutures. In order to secure sufficient bladder capacity, we estimated the minimum residual volume as 21 ml after bladder plasty. The remaining bladder capacity was confirmed to be 30 ml by injecting a contrast dye and saline into the bladder. The neonate had no associated cardiac urogenital or skeletal anomalies. Postoperative course was uneventful. The patient was regularly followed up for two years after surgery and underwent umbilicoplasty. He had no trouble with urinary function. Conclusion In this case, we experienced extremely rare condition of a small omphalocele with bladder evagination associated with urachal aplasia and reviewed 7 case reports of anomalies similar to those in the present case. Umbilical cord cysts may be an informative indicator of these symptoms in utero. Therefore, ultrasonography scans should be conducted until delivery, despite the spontaneous disappearance of cord cysts. |
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| 言語 | en | |||||||||||||||
| 出版者 | ||||||||||||||||
| 出版者 | SpringerOpen | |||||||||||||||
| 言語 | en | |||||||||||||||
| 言語 | ||||||||||||||||
| 言語 | eng | |||||||||||||||
| 資源タイプ | ||||||||||||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||||||||||||
| 資源タイプ | journal article | |||||||||||||||
| 出版タイプ | ||||||||||||||||
| 出版タイプ | VoR | |||||||||||||||
| 出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||||||||||||
| 関連情報 | ||||||||||||||||
| 識別子タイプ | DOI | |||||||||||||||
| 関連識別子 | https://doi.org/10.1186/s40792-023-01710-y | |||||||||||||||
| 収録物識別子 | ||||||||||||||||
| 収録物識別子タイプ | EISSN | |||||||||||||||
| 収録物識別子 | 2198-7793 | |||||||||||||||
| 収録物名 | ||||||||||||||||
| 収録物名 | Surgical Case Reports | |||||||||||||||
| 言語 | en | |||||||||||||||
| 書誌情報 |
巻 9, p. 1-6, 発行日 2023-07-10 |
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Cite as
Kobayashi, Haruka, Baba, Tokuro, Kuda, Masaaki, Ieiri, Satoshi, Takatsuki, Mitsuhisa, n.d., Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case: SpringerOpen.
