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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.

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。

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