A Rare Case Report of Encephalocele with Numerous Ependymal Components: A Potential Diagnostic Pitfall

脑膨出 室管膜 室管膜细胞 解剖 病理 医学 免疫组织化学 中枢神经系统 内分泌学
作者
Chenglong Wang,Jin Zhu,Yan Zeng,Xue Qin,Yiwen Tan,Min Zeng,Lijuan Wang,Xiaojing Cao,Lingfeng Zou,Youde Cao
出处
期刊:International Journal of Surgical Pathology [SAGE Publishing]
卷期号:29 (1): 85-89 被引量:1
标识
DOI:10.1177/1066896920925146
摘要

Different cellular constituents of the central nervous system occurring in encephaloceles or neuroglial heterotopias (NGHs) have been reported, but the ependymal morphology has rarely been described in the previous literature, let alone the related histological images. To determine the ependymal morphology in encephaloceles or NGHs, we report a rare case of encephalocele with numerous ependymal components. Radiological examination showed that a 6.2 × 3.1 cm nasal dorsum mass-forming encephalocele in a 24-year-old woman, who had an intracranial connection through a frontal bone defect. This patient underwent a resection of the encephalocele under nasal endoscopy and a reconstruction of the cranial base. The patient had a good prognosis with no postoperative complications during follow-up. Microscopically, the ependymal components entrapped in a collagenized background showed numerous slit-like spaces lined by columnar cells with abundant palely eosinophilic cytoplasm and apical surface microvilli. With immunohistochemistry, in addition to the expression of EMA along with the slit-like spaces, GFAP and S100 were diffusely expressed in the slit-like spaces. In conclusion, the ependymal component in either encephaloceles or NGHs may present slit-like spaces arranged in an anastomosing pattern. The unusual morphology of ependyma continues to be underrecognized by pathologists and is easily misdiagnosed; therefore, an awareness of the morphological change in ependyma is necessary.
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