Giordana M T, Bradac G B, Pagni C A, Marino S, Attanasio A
Department of Neurology, University of Turin, Italy.
Acta Neurochir (Wien). 1995;132(1-3):154-9. doi: 10.1007/BF01404866.
A case of primary diffuse leptomeningeal gliomatosis with anaplastic features, diagnosed during life and confirmed at autopsy, is presented. The clinical, radiological and pathological features are compared with those of the very few cases reported in the literature. Early papilloedema and hydrocephalus were followed by spinal and cranial nerve palsies. The NMR images and the tissue biopsy turned out to be useful for reaching an in vivo diagnosis. While in the previously reported cases the glial proliferation was microscopically a slow growing astrocytoma, the present case was histologically malignant and had a high labelling index (LIs) for proliferation markers (PCNA and KI-67). The high growth rate and the wide diffusion of the tumour at presentation may account for the poor prognosis of diffuse leptomeningeal gliomatosis and the inefficacy of radiotherapy and chemotherapy. The presence of basal lamina arount tumour cells and the immunohistochemical distribution of the proliferation markers are consistent with the origin of primary leptomeningeal gliomatosis from ectopic glia.
本文报告一例生前诊断并经尸检证实的具有间变特征的原发性弥漫性软脑膜胶质瘤病。将其临床、放射学和病理学特征与文献中报道的极少数病例进行了比较。早期出现视乳头水肿和脑积水,随后出现脊髓和颅神经麻痹。核磁共振成像和组织活检结果证明对进行活体诊断有用。在先前报道的病例中,胶质细胞增生在显微镜下是生长缓慢的星形细胞瘤,而本例在组织学上是恶性的,增殖标志物(PCNA和KI-67)的标记指数(LIs)很高。肿瘤在出现时的高生长率和广泛扩散可能是弥漫性软脑膜胶质瘤病预后不良以及放疗和化疗无效的原因。肿瘤细胞周围基底膜的存在以及增殖标志物的免疫组化分布与原发性软脑膜胶质瘤病起源于异位神经胶质一致。