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幕上神经肠囊肿的恶性转化:一例报告及文献复习

Malignant Transformation of a Supratentorial Neurenteric Cyst: A Case Report and Literature Review.

作者信息

Alanazi Nura, Sayed Ahmed Gamal, Hassounah Maher, Dababo Mohammad

机构信息

Department of Pathology and Laboratory Medicine, King Saud University Medical City, Riyadh, SAU.

College of Medicine, Alfaisal University College of Medicine, Riyadh, SAU.

出版信息

Cureus. 2025 Jun 11;17(6):e85781. doi: 10.7759/cureus.85781. eCollection 2025 Jun.

Abstract

Neurenteric cysts (NECs) are congenital lesions of endodermal origin that are uncommon, and malignant transformation is extremely rare. They are predominantly found in the spinal subdural space. We report a case of a 50-year-old female with a known history of hypothyroidism, presenting with a nine-month history of severe occipital headache, neck pain, and rigidity, accompanied by a notable unintentional weight loss of 20 kg. Neurological examination was unremarkable. Imaging studies revealed a complex multilobulated cystic lesion involving the velum interpositum and the trigone of the left lateral ventricle. Diffuse craniocervical spinal cord leptomeningeal enhancement was identified. Lumbar puncture confirmed rare, atypical epithelial cells. Gross total resection of the tumor was done through a parietal craniotomy. Histopathological examination revealed transitional features of a neurenteric cyst from benign to malignant, supported by morphological and immunohistochemical findings. Neurenteric cysts, though rare in supratentorial or infratentorial locations, should be included in the differential diagnosis of intracranial cysts. The presence of benign epithelium and dysplastic epithelium with malignant features, together with a high proliferation index, indicates malignant transformation of the neurenteric cyst. To the best of our knowledge, this is the fourth case reported so far that is distinct regarding location, with the velum interpositum and the trigone of the left lateral ventricle rarely being reported sites.

摘要

神经管肠囊肿(NECs)是一种起源于内胚层的先天性病变,较为罕见,恶性转化极为罕见。它们主要见于脊髓硬膜下间隙。我们报告一例50岁女性患者,有甲状腺功能减退病史,出现严重枕部头痛、颈部疼痛和僵硬9个月,伴有明显的非故意体重减轻20kg。神经系统检查无异常。影像学检查显示一个复杂的多叶囊性病变,累及中间帆和左侧脑室三角区。发现弥漫性颅颈脊髓软脑膜强化。腰椎穿刺证实有罕见的非典型上皮细胞。通过顶骨开颅术对肿瘤进行了全切除。组织病理学检查显示神经管肠囊肿从良性到恶性的过渡特征,形态学和免疫组化结果支持这一结论。神经管肠囊肿虽然在幕上或幕下部位罕见,但在颅内囊肿的鉴别诊断中应予以考虑。良性上皮和具有恶性特征的发育异常上皮的存在,以及高增殖指数,表明神经管肠囊肿发生了恶性转化。据我们所知,这是迄今为止报道的第四例在位置上有独特之处的病例,中间帆和左侧脑室三角区很少被报道为发病部位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7899/12249479/04ed402b26e4/cureus-0017-00000085781-i01.jpg

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