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  Vol. 38 No. 10, October 1981 TABLE OF CONTENTS
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Primary Leptomeningeal Gliomatosis

Symptoms Suggestive of Meningitis

Khang-Loon Ho, MD; Judith A. Hoschner, MD; David E. Wolfe, MD

Arch Neurol. 1981;38(10):662-666.


Abstract

• Gliomas that arise primarily in the leptomeninges are rare. Of the 15 reported cases of primary leptomeningeal glioma, only two diffusely involved the leptomeninges. We report the third case of primary leptomeningeal gliomatosis, this in a 55-year-old man who died three months after the onset of symptoms. The clinical manifestations, CSF findings, and the gross appearance of the brain resembled meningitis rather than neoplasm. Results of cytologic examinations of the CSF were normal and the diagnosis was made at necropsy. The diffuse form of primary leptomeningeal glioma has a shorter clinical course and poorer prognosis than the solitary form. Primary leptomeningeal gliomas are believed to arise from heterotopic neuroglial tissue in the leptomeninges.



Author Affiliations

From the Department of Pathology (Neuropathology) (Drs Ho and Wolfe), Wayne State University School of Medicine; and the Department of Pathology (Dr Hoschner), Harper-Grace Hospital, Detroit.


Footnotes

Accepted for publication Feb 28, 1981.

Reprint requests to Department of Pathology, Scott Hall, 540 E Canfield, Detroit, MI 48201 (Dr Ho).



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Primary diffuse leptomeningeal gliomatosis: unusual MRI with non-enhancing nodular lesions on the cerebellar surface and spinal leptomeningeal enhancement
Kastenbauer et al.
J. Neurol. Neurosurg. Psychiatry 2000;69:385-388.
ABSTRACT | FULL TEXT  





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