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. 2016:2016:5016840.
doi: 10.1155/2016/5016840. Epub 2016 Nov 7.

Primary Diffuse Leptomeningeal Gliomatosis: Radiological/Pathological Features

Affiliations

Primary Diffuse Leptomeningeal Gliomatosis: Radiological/Pathological Features

Ehtasham Ahmad et al. Case Rep Neurol Med. 2016.

Abstract

We present the case of a 43-year-old lady who presented with headaches, visual impairment, and seizures, progressing rapidly over the course of a few weeks. Extensive workup excluded an inflammatory or infectious cause. Imaging studies revealed diffuse thickening of the leptomeninges and serial CSF analysis showed raised opening pressures and increased protein levels. A diagnostic biopsy of the lower thoracic dura confirmed the diagnosis of primary diffuse leptomeningeal gliomatosis (PDGL). She was managed supportively for her symptoms and unfortunately she passed away a few weeks later.

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Conflict of interest statement

The authors declare that there are no competing interests regarding the publication of this paper.

Figures

Figure 1
Figure 1
Axial head CT.
Figure 2
Figure 2
Axial head MRI.
Figure 3
Figure 3
Sagittal head MRI.
Figure 4
Figure 4
Spine MRI, thoracic region.
Figure 5
Figure 5
Spine MRI, lumbosacral region.
Figure 6
Figure 6
The biopsy from the lower thoracic dura showed fibrous tissue lined by meningothelial type of cells with nests of moderately pleomorphic cells. These cells appeared fibrillary, rounded, and occasionally gemistocytic or multinucleated. Proliferating vascular clusters were present as well. Occasional round cells were seen forming clusters in plane.

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