Autor: J. Pialat, R. Duthel, Patrick Beauchesne, G. Clavreul, F. G. Barral, B. Laurent, T. Schmitt
Rok vydání: 1998
Předmět:
Zdroj: Journal of Neuro-Oncology. 37:161-167
ISSN: 0167-594X
DOI: 10.1023/a:1005888319228
Popis: Primary leptomeningeal gliomatosis is rare, and the diffuse form (PLDG) is even more unusual. The following report is an example. A 17 year-old man developed a syndrome characterized by extensive basal and chronic spinal meningitis. Routine biological tests showed elevated levels of CSF proteins, and moderate mononuclear pleocytosis, with no direct evidence of neoplasia, leading to a diagnosis of chronic meningitis. A second meningeal biopsy, guided by MRI and performed in the left frontal region, led to the specific diagnosis of primary diffuse leptomeningeal gliomatosis. Treatment including ventricular and lumbar shunting, a course of cortico-spinal radiation, and three courses of an eight-drug systemic chemotherapy with intrathecal methotrexate lead to complete remission over 15 months. We believe that this is the first report of such a remission in the literature.
Databáze: OpenAIRE