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原发性软脑膜少突胶质细胞瘤病

Primary leptomeningeal oligodendrogliomatosis.

作者信息

Mathews Marlon S, Paré Laura S, Kuo Jeffery V, Kim Ronald C

机构信息

Department of Neurological Surgery, State University New York at Buffalo, Buffalo, USA.

出版信息

J Neurooncol. 2009 Sep;94(2):275-8. doi: 10.1007/s11060-009-9821-8. Epub 2009 Mar 17.

Abstract

Primary leptomeningeal oligodendrogliomas (PLOs) are rare intracranial malignancies where tumors grow in the subarachnoid space without an obvious connection to the brain or spinal cord parenchyma. Adding to the three previously reported cases of PLO with no parenchymal involvement we report a fourth case of the same in this paper in a 50-year-old woman presenting with unrelenting headaches. CT scan of her head revealed hydrocephalus and MRI revealed diffuse enhancement of her leptomeninges throughout her brain and spine, prominent over the basilar region. Biopsy obtained using a frameless stereotactic biopsy showed sharply defined cell borders, clear cytoplasm, and rounded nuclei consistent with an oligodendroglioma. Our case suggests that PLO can mimic diffuse forms of granulomatous meningitis and should be suspected in patients that clinically and radiographically present like granulomatous meningitis but without blood or CSF markers for the same.

摘要

原发性软脑膜少突胶质细胞瘤(PLO)是一种罕见的颅内恶性肿瘤,肿瘤在蛛网膜下腔生长,与脑实质或脊髓实质无明显联系。除了之前报道的3例无实质受累的PLO病例外,我们在本文中报告了第4例,患者为一名50岁女性,伴有持续性头痛。她的头部CT扫描显示脑积水,MRI显示其整个脑和脊髓的软脑膜弥漫性强化,在基底区域尤为明显。使用无框架立体定向活检获得的活检结果显示,细胞边界清晰、细胞质透明、细胞核呈圆形,符合少突胶质细胞瘤的特征。我们的病例表明,PLO可模仿肉芽肿性脑膜炎的弥漫形式,对于临床和影像学表现类似肉芽肿性脑膜炎但无相关血液或脑脊液标志物的患者应怀疑此病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/2724631/c192065cb921/11060_2009_9821_Fig1_HTML.jpg

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