儿童尾沟囊肿:病例报告和文献综述。

Ramendra Shukla, Jay Divyesh Patel, Sudhir B Chandna, Urvish Parikh
{"title":"儿童尾沟囊肿:病例报告和文献综述。","authors":"Ramendra Shukla, Jay Divyesh Patel, Sudhir B Chandna, Urvish Parikh","doi":"10.4103/ajps.ajps_82_23","DOIUrl":null,"url":null,"abstract":"<p><strong>Abstract: </strong>Tailgut cysts are rare congenital abnormalities that develop due to failure of embryologic tailgut to involute. This generally manifests as a presacral, retrorectal and multicystic mass. It has a high propensity in female patients including paediatric age group. The clinical presentation varies depending on the age of patient, location and size of the cyst. The symptoms are mostly due to mass effects and rarely complications such as malignancy. Being a rare entity, it is generally misdiagnosed. Differential diagnosis mostly includes rectal duplication cyst, sacrococcygeal teratoma and anterior meningocele. Radiological imaging such as computed tomography scan and magnetic resonance imaging is useful in the diagnosis. The treatment of choice is complete excision to prevent recurrence, infection and malignant degeneration. We have reviewed previous literature and given our valuable information regarding the same.</p>","PeriodicalId":72123,"journal":{"name":"African journal of paediatric surgery : AJPS","volume":"21 3","pages":"184-187"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11379328/pdf/","citationCount":"0","resultStr":"{\"title\":\"Tailgut Cyst in a Child: A Case Report and Review of Literature.\",\"authors\":\"Ramendra Shukla, Jay Divyesh Patel, Sudhir B Chandna, Urvish Parikh\",\"doi\":\"10.4103/ajps.ajps_82_23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Abstract: </strong>Tailgut cysts are rare congenital abnormalities that develop due to failure of embryologic tailgut to involute. This generally manifests as a presacral, retrorectal and multicystic mass. It has a high propensity in female patients including paediatric age group. The clinical presentation varies depending on the age of patient, location and size of the cyst. The symptoms are mostly due to mass effects and rarely complications such as malignancy. Being a rare entity, it is generally misdiagnosed. Differential diagnosis mostly includes rectal duplication cyst, sacrococcygeal teratoma and anterior meningocele. Radiological imaging such as computed tomography scan and magnetic resonance imaging is useful in the diagnosis. The treatment of choice is complete excision to prevent recurrence, infection and malignant degeneration. We have reviewed previous literature and given our valuable information regarding the same.</p>\",\"PeriodicalId\":72123,\"journal\":{\"name\":\"African journal of paediatric surgery : AJPS\",\"volume\":\"21 3\",\"pages\":\"184-187\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11379328/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"African journal of paediatric surgery : AJPS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ajps.ajps_82_23\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/9 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"African journal of paediatric surgery : AJPS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ajps.ajps_82_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/9 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

摘要:尾肠囊肿是一种罕见的先天性畸形,由于胚胎尾肠未能内卷而形成。一般表现为骶前部、直肠后部和多囊性肿块。该病好发于女性患者,包括儿童。临床表现因患者年龄、囊肿位置和大小而异。症状多为肿块效应,很少有并发症,如恶性肿瘤。由于这种疾病比较罕见,因此通常会被误诊。鉴别诊断主要包括直肠重复囊肿、骶尾部畸胎瘤和前脑膜囊肿。计算机断层扫描和磁共振成像等放射影像学检查有助于诊断。首选的治疗方法是彻底切除,以防止复发、感染和恶性变。我们回顾了以往的文献,并提供了有价值的相关信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tailgut Cyst in a Child: A Case Report and Review of Literature.

Tailgut Cyst in a Child: A Case Report and Review of Literature.

Tailgut Cyst in a Child: A Case Report and Review of Literature.

Abstract: Tailgut cysts are rare congenital abnormalities that develop due to failure of embryologic tailgut to involute. This generally manifests as a presacral, retrorectal and multicystic mass. It has a high propensity in female patients including paediatric age group. The clinical presentation varies depending on the age of patient, location and size of the cyst. The symptoms are mostly due to mass effects and rarely complications such as malignancy. Being a rare entity, it is generally misdiagnosed. Differential diagnosis mostly includes rectal duplication cyst, sacrococcygeal teratoma and anterior meningocele. Radiological imaging such as computed tomography scan and magnetic resonance imaging is useful in the diagnosis. The treatment of choice is complete excision to prevent recurrence, infection and malignant degeneration. We have reviewed previous literature and given our valuable information regarding the same.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信