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颅内胎中胎——一种儿科罕见病。

Intracranial Fetus In Fetu-a Pediatric Rarity.

机构信息

Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, Delhi, India.

Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, Delhi, India.

出版信息

World Neurosurg. 2020 Jul;139:286-288. doi: 10.1016/j.wneu.2020.03.156. Epub 2020 Apr 2.

DOI:10.1016/j.wneu.2020.03.156
PMID:32247796
Abstract

BACKGROUND

Intracranial fetus in fetu is an extremely rare entity in which a discrete vertebrate fetiform mass is found inside a diamniotic, monochorionic twin. It is a benign mass and can manifest with symptoms owing to mass effect. To establish the diagnosis, a vertebra must be present within the mass.

CASE DESCRIPTION

A 5-year-old child presented at a multispecialty hospital with gradual weakness of both lower limbs. Magnetic resonance imaging of the brain revealed a midline intraventricular mass with lobulated margins having both cystic and fatty components with areas of blooming within. A provisional diagnosis of teratoma/primitive neuroectodermal tumor was made. The patient subsequently presented to our hospital with drowsiness and vomiting for 1 day. Noncontrast computed tomography revealed a mass of heterogeneous density occupying the third ventricle. The mass contained a few well-formed long bones representative of the appendicular skeleton and a vertebra-like bone representative of the axial skeleton, fulfilling the Willis criteria. A biopsy sample was taken from the mass; no malignant cells were seen on histopathologic examination. Based on noncontrast computed tomography findings of well-formed long bones and a vertebra and no significant increase in the size of the mass over 2 years, an intracranial fetus in fetu was diagnosed.

CONCLUSIONS

Whenever bony structures are identified in an intracranial mass in a pediatric patient, we should always look for bones of the axial skeleton, as this finding will point toward a diagnosis of intracranial fetus in fetu and will help in differentiating it from teratoma, which can have malignant transformation.

摘要

背景

颅内胎中胎是一种极为罕见的疾病,在这种疾病中,一个独立的脊椎胎儿样肿块被发现在一个双羊膜囊、单绒毛膜的双胞胎内。它是一种良性肿块,可能由于肿块效应而出现症状。为了建立诊断,肿块内必须存在一个椎骨。

病例描述

一名 5 岁儿童因双侧下肢逐渐无力在一家多专科医院就诊。脑部磁共振成像显示一个中线脑室室内肿块,边缘呈分叶状,具有囊性和脂肪性成分,并有区域内信号增强。初步诊断为畸胎瘤/原始神经外胚层肿瘤。随后,该患者因嗜睡和呕吐 1 天就诊于我们医院。非增强 CT 显示一个混杂密度的肿块占据第三脑室。肿块内有几个形态良好的长骨,代表附肢骨骼,还有一个类似椎骨的骨骼,代表轴骨骼,符合 Willis 标准。从肿块中取了一个活检样本;组织病理学检查未见恶性细胞。根据非增强 CT 显示的形态良好的长骨和一个椎骨,以及肿块在 2 年期间没有明显增大的情况,诊断为颅内胎中胎。

结论

无论何时在儿科患者的颅内肿块中发现骨结构,我们都应该寻找轴骨骼的骨骼,因为这一发现将指向颅内胎中胎的诊断,并有助于将其与可能发生恶性转化的畸胎瘤区分开来。

相似文献

1
Intracranial Fetus In Fetu-a Pediatric Rarity.颅内胎中胎——一种儿科罕见病。
World Neurosurg. 2020 Jul;139:286-288. doi: 10.1016/j.wneu.2020.03.156. Epub 2020 Apr 2.
2
Intraventricular twin fetuses in fetu.胎儿体内的脑室双胞胎胎儿。
J Neurosurg Pediatr. 2012 Jan;9(1):17-23. doi: 10.3171/2011.10.PEDS11196.
3
Fetus in fetu in an adult: diagnosis by computed tomography imaging.成人身体内的胎中胎:通过计算机断层扫描成像进行诊断
J Formos Med Assoc. 2005 Mar;104(3):203-5.
4
Fetus-in-fetu: a rare entity.胎中胎:一种罕见的实体。
Fetal Diagn Ther. 2007;22(3):195-7. doi: 10.1159/000098716. Epub 2007 Jan 17.
5
[Endoparasite twin (fetus in fetu)].[体内寄生胎(胎中胎)]
Ginekol Pol. 2005 Mar;76(3):228-33.
6
Twin fetus in fetu with immature teratoma: a case report and review of the literature.胎儿内胎儿伴未成熟畸胎瘤:一例报告并文献复习
Arch Iran Med. 2009 Sep;12(5):507-10.
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From observation to aetiology: a case report of a twin fetus-in-fetu and a revisit of the known rarity.从观察到病因:双胎寄生胎一例报告及对已知罕见病例的再探讨
Hong Kong Med J. 2015 Feb;21(1):80-3. doi: 10.12809/hkmj133925.
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Diagnostic dilemma in a neglected case of fetus-in-fetu solved with Magnetic Resonance Imaging and MDCT--a case report and review of literature.磁共振成像和多层螺旋CT解决的一例被忽视的胎中胎诊断难题——病例报告及文献复习
J Radiol Case Rep. 2011;5(10):29-37. doi: 10.3941/jrcr.v5i10.833. Epub 2011 Oct 1.
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Fetus-in-fetu: a case report with molecular analysis.胎内胎:一例分子分析病例报告
J Pediatr Surg. 1999 Apr;34(4):641-4. doi: 10.1016/s0022-3468(99)90095-7.
10
Fetus-in-fetu in the cranium of a 4-month-old boy: histopathology and short tandem repeat polymorphism-based genotyping. Case report.一名4个月大男婴颅骨内的胎内胎:组织病理学及基于短串联重复序列多态性的基因分型。病例报告。
J Neurosurg Pediatr. 2008 May;1(5):410-4. doi: 10.3171/PED/2008/1/5/410.

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