“Human tail”: Case reports of coccyx retroposition in children

S. Trofimova, D. S. Buklaev, T. Murashko
{"title":"“Human tail”: Case reports of coccyx retroposition in children","authors":"S. Trofimova, D. S. Buklaev, T. Murashko","doi":"10.17816/ptors397591","DOIUrl":null,"url":null,"abstract":"BACKGROUND:Ahuman tail isarare congenital malformation that corresponds to the protrusion on the dorsal side of the lumbar, sacrococcygeal, and paraanal regions. This study aimed to demonstrate three rare clinical cases ofatail-shaped formation caused by the protrusion ofanelongated coccyx in children. \nCLINICAL CASES:These patients asked for medical assistance for pain felt in the sitting position and daily discomfort because this formation barely contains any tissues other than the coccyx. The patients had no signs of neurological and lower urinary tract insufficiency. In all cases, the retroposition of the coccyx without its typical anterior angulation was determined based on radiographic and magnetic resonance imaging (MRI) signs. In one case, the coccyx was represented by four elongated vertebrae withoutatypical decrease in the size of the vertebrae in the caudal direction. In two cases,anangular deformity of the coccyx occurred at the level of CoIIIwith intercoccygeal angles of 138 and 140. \nDISCUSSION:The tail-like formations could be classified as pseudo-tails according to the classification by Dao and Netsky (1984) and type Ia human tails according to the classification by Tojima and Yamada (2020). \nCONCLUSIONS:The most important feature of tail-shaped formation is the connection with occult dysraphic malformations, which requiresacomprehensive preoperative examination in each case (neurological examination, radiography, computed tomography, and MRI). Careless surgery may lead to serious consequences that significantly impair patients quality of life.","PeriodicalId":37631,"journal":{"name":"Pediatric Traumatology, Orthopaedics and Reconstructive Surgery","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Traumatology, Orthopaedics and Reconstructive Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17816/ptors397591","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND:Ahuman tail isarare congenital malformation that corresponds to the protrusion on the dorsal side of the lumbar, sacrococcygeal, and paraanal regions. This study aimed to demonstrate three rare clinical cases ofatail-shaped formation caused by the protrusion ofanelongated coccyx in children. CLINICAL CASES:These patients asked for medical assistance for pain felt in the sitting position and daily discomfort because this formation barely contains any tissues other than the coccyx. The patients had no signs of neurological and lower urinary tract insufficiency. In all cases, the retroposition of the coccyx without its typical anterior angulation was determined based on radiographic and magnetic resonance imaging (MRI) signs. In one case, the coccyx was represented by four elongated vertebrae withoutatypical decrease in the size of the vertebrae in the caudal direction. In two cases,anangular deformity of the coccyx occurred at the level of CoIIIwith intercoccygeal angles of 138 and 140. DISCUSSION:The tail-like formations could be classified as pseudo-tails according to the classification by Dao and Netsky (1984) and type Ia human tails according to the classification by Tojima and Yamada (2020). CONCLUSIONS:The most important feature of tail-shaped formation is the connection with occult dysraphic malformations, which requiresacomprehensive preoperative examination in each case (neurological examination, radiography, computed tomography, and MRI). Careless surgery may lead to serious consequences that significantly impair patients quality of life.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
“人尾”:儿童尾骨后移病例报告
背景:一种人尾异位先天性畸形,对应于腰椎背部、骶尾骨和肛门旁区域的突出。本研究的目的是展示三个罕见的临床病例尾形形成引起的延长尾骨突出的儿童。临床病例:这些患者因坐位疼痛和日常不适而要求医疗协助,因为这种形成除了尾骨外几乎没有任何组织。患者没有神经系统和下尿路功能不全的症状。在所有病例中,没有典型前角的尾骨后移是根据x线摄影和磁共振成像(MRI)征象确定的。在一个病例中,尾骨表现为四个细长的椎骨,在尾骨方向上没有椎骨大小的非典型减小。在两个病例中,尾骨角畸形发生在coiii水平,尾骨间角分别为138和140。讨论:根据Dao和Netsky(1984)的分类,类尾构造可分为伪尾,根据Tojima和Yamada(2020)的分类,可分为Ia型人尾。结论:尾形畸形最重要的特征是与隐性发育不良畸形的联系,需要对每例患者进行全面的术前检查(神经学检查、x线摄影、计算机断层扫描和MRI)。粗心的手术可能会导致严重的后果,严重影响患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
38
期刊介绍: The target audience of the journal is researches, physicians, orthopedic trauma, burn, and pediatric surgeons, anesthesiologists, pediatricians, neurologists, oral surgeons, and all specialists in related fields of medicine.
期刊最新文献
Pitfalls and complications in the treatment of clubfoot by the Ponseti method: A literature review Dynamics of feet dorsiflexion after percutaneous Achilles lengthening for correction of flat feet in children Musculoskeletal injuries and pain in children involved in sports: A literature review Risk factors for the development of congenital giant nevi in children Comparative analysis of the detection of diseases of the muscular system in minors of Saint Petersburg
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1