Foetus-in-foetu versus Well-differentiated Sacrococcygeal Teratoma: A Pathological Dilemma

Sufian Zaheer, Durre Aden, Swati Bhardwaj, AmitKumar Yadav
{"title":"Foetus-in-foetu versus Well-differentiated Sacrococcygeal Teratoma: A Pathological Dilemma","authors":"Sufian Zaheer, Durre Aden, Swati Bhardwaj, AmitKumar Yadav","doi":"10.4103/hmj.hmj_35_23","DOIUrl":null,"url":null,"abstract":"Rationale: Foetus-in-foetu (FIF) is a rare congenital anomaly seen in young infants or at birth. It is a parasitic twin in a diamniotic, monozygotic twin. It needs to be differentiated from teratoma, as the latter has malignant potential. Patient Concern: Here, we present a case of an 11-day-old infant presenting with mass abdomen since birth. Microscopic examination showed skin with adnexal structures, neural, respiratory, gastrointestinal tissue, cartilage, bone and ocular structures also identified, which showed normal histology with the same degree of maturation. Diagnosis: A diagnosis of FIF was reported based on the radiological which was confirmed on histopathology. Outcome: The patient is doing well post-surgery. Lessons: This case highlights the significance of radiological, clinical, intraoperative and pathological features that help distinguish the two conditions.","PeriodicalId":34280,"journal":{"name":"Hamdan Medical Journal","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hamdan Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/hmj.hmj_35_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Rationale: Foetus-in-foetu (FIF) is a rare congenital anomaly seen in young infants or at birth. It is a parasitic twin in a diamniotic, monozygotic twin. It needs to be differentiated from teratoma, as the latter has malignant potential. Patient Concern: Here, we present a case of an 11-day-old infant presenting with mass abdomen since birth. Microscopic examination showed skin with adnexal structures, neural, respiratory, gastrointestinal tissue, cartilage, bone and ocular structures also identified, which showed normal histology with the same degree of maturation. Diagnosis: A diagnosis of FIF was reported based on the radiological which was confirmed on histopathology. Outcome: The patient is doing well post-surgery. Lessons: This case highlights the significance of radiological, clinical, intraoperative and pathological features that help distinguish the two conditions.
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
胎中胎与分化良好的骶尾畸胎瘤:病理困境
理由:胎中胎(FIF)是一种罕见的先天性异常,见于婴儿或出生时。它是双胎同卵双胞胎中的寄生双胞胎。需与畸胎瘤鉴别,畸胎瘤有恶性潜能。病人关注:在这里,我们提出一个11天大的婴儿自出生以来出现肿块腹部的病例。镜检发现皮肤有附件结构,神经、呼吸、胃肠组织、软骨、骨和眼部结构,组织学正常,成熟程度相同。诊断:经组织病理证实,影像学诊断为FIF。结果:患者术后恢复良好。经验教训:本病例强调了放射学、临床、术中和病理特征的重要性,这些特征有助于区分两种情况。
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
自引率
0.00%
发文量
22
审稿时长
24 weeks
期刊最新文献
Isolated amoebic splenic abscess: A case report on rare entity and diagnostic challenge Patient with complete heart block without pacemaker for surgery: An anaesthetist's nightmare Hypoxia is associated with increased expression of APOBEC genes in breast cancer Paranasal sinus mucoceles: A narrative review Two interesting cases of a rare haemoglobin variant – Haemoglobin J Meerut with varied clinical presentations
×
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