Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, Delhi, India.
Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, Delhi, India.
World Neurosurg. 2020 Jul;139:286-288. doi: 10.1016/j.wneu.2020.03.156. Epub 2020 Apr 2.
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.
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.
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.
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。
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。
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。