TY - JOUR
T1 - Spinal low-grade neoplasms with extensive leptomeningeal dissemination in children
AU - Perilongo, Giorgio
AU - Gardiman, Marina
AU - Bisaglia, Lucia
AU - Rigobello, Luca
AU - Calderone, Milena
AU - Battistella, Antonio
AU - Burnelli, Roberta
AU - Giangaspero, Felice
PY - 2002/10
Y1 - 2002/10
N2 - Objective: The aim of this study is to re-appraise paediatric leptomeningeal disseminated spinal low-grade neoplasms putting forward the hypothesis that these tumours may represent a possible distinctive clinico-pathological entity. Case report: Three children affected by these rare neoplasms are reported, 2 boys and 1 girl aged 40 months, 7 and 12 years respectively. Results: Despite treatment, 2 died at 9 months and 9 years, while 1 has survived with stable disease at 24 months after diagnosis. Histologically, these tumours shared the generic histological appearance of low-grade neuroectodermal neoplasms, without any features that allowed them to be included in a specific classification niche. The magnetic resonance imaging of the leptomeningeal dissemination took the form of a thick, diffuse subarachnoidal enhancement involving the brain as well the spine in 2 patients; in 1 patient there was an extensive enhancement along the surface of the brain and of the spinal cord and multiple small cysts, creating the impression of a diffuse microcystic meningoencephalopathy. Discussion: The patients described here and the similar ones found in the literature cannot be easily placed into the present WHO system of classification for central nervous system tumours.
AB - Objective: The aim of this study is to re-appraise paediatric leptomeningeal disseminated spinal low-grade neoplasms putting forward the hypothesis that these tumours may represent a possible distinctive clinico-pathological entity. Case report: Three children affected by these rare neoplasms are reported, 2 boys and 1 girl aged 40 months, 7 and 12 years respectively. Results: Despite treatment, 2 died at 9 months and 9 years, while 1 has survived with stable disease at 24 months after diagnosis. Histologically, these tumours shared the generic histological appearance of low-grade neuroectodermal neoplasms, without any features that allowed them to be included in a specific classification niche. The magnetic resonance imaging of the leptomeningeal dissemination took the form of a thick, diffuse subarachnoidal enhancement involving the brain as well the spine in 2 patients; in 1 patient there was an extensive enhancement along the surface of the brain and of the spinal cord and multiple small cysts, creating the impression of a diffuse microcystic meningoencephalopathy. Discussion: The patients described here and the similar ones found in the literature cannot be easily placed into the present WHO system of classification for central nervous system tumours.
KW - Children
KW - Leptomeningeal dissemination
KW - Low-grade glioma
KW - Spinal tumours
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U2 - 10.1007/s00381-002-0626-8
DO - 10.1007/s00381-002-0626-8
M3 - Article
C2 - 12382176
AN - SCOPUS:0036817795
SN - 0256-7040
VL - 18
SP - 505
EP - 512
JO - Child's Nervous System
JF - Child's Nervous System
IS - 9-10
ER -