Ko Melissa W, Turkeltaub Peter E, Lee Edward B, Gonatas Nicholas K, Volpe Nicholas J, Moster Mark L, Galetta Steven L
Department of Neurology, State University of New York Upstate Medical University, Syracuse, NY 13202, USA.
J Neurol Sci. 2009 Mar 15;278(1-2):127-31. doi: 10.1016/j.jns.2008.11.026. Epub 2009 Jan 8.
Primary diffuse leptomeningeal gliomatosis (PDLG) is a rare, fatal, neoplastic condition of infiltrating glial cells into the meninges without evidence of primary tumor in the brain or spinal cord parenchyma. Primary diffuse leptomeningeal gliomatosis often presents with symptoms and physical findings of chronic inflammatory meningitis and raised intracranial pressure, and lacks specific clinical, radiologic, and diagnostic criteria. We report a case of PDLG diagnosed post-mortem, highlighting the diagnostic difficulty in identifying PDLG as the cause of chronic meningitis, even when a neoplastic etiology is suspected. Because multiple cytologies and even a leptomeningeal biopsy did not reveal the diagnosis ante-mortem, we emphasize the consideration of multi-site or repeat leptomeningeal biopsy when a persistent inflammatory infiltrate is found and neurological symptoms are progressive.
原发性弥漫性软脑膜胶质瘤病(PDLG)是一种罕见的、致命的肿瘤性疾病,其特征为胶质细胞浸润至脑膜,而脑实质或脊髓实质内无原发性肿瘤证据。原发性弥漫性软脑膜胶质瘤病常表现为慢性炎症性脑膜炎的症状和体征以及颅内压升高,且缺乏特异性的临床、影像学和诊断标准。我们报告一例死后诊断为PDLG的病例,强调即使怀疑为肿瘤性病因,识别PDLG作为慢性脑膜炎病因的诊断困难。由于多次细胞学检查甚至软脑膜活检均未在生前明确诊断,我们强调当发现持续性炎症浸润且神经症状呈进行性发展时,应考虑进行多部位或重复软脑膜活检。