Oligodendroglioma and multiple sclerosis. A case report
The concurrence of multiple sclerosis (MS) and glioma is uncommon. Approximately 30 cases have been reported, but in only six of them the tumour was pure or mixed oligodendroglioma. The appearance of new neurological symptoms and signs in a patient with multiple sclerosis is usually attributed to a...
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Veröffentlicht in: | Neurocirugía (Asturias, Spain) Spain), 2004-08, Vol.15 (4), p.378-383 |
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Sprache: | eng |
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Zusammenfassung: | The concurrence of multiple sclerosis (MS) and glioma is uncommon. Approximately 30 cases have been reported, but in only six of them the tumour was pure or mixed oligodendroglioma. The appearance of new neurological symptoms and signs in a patient with multiple sclerosis is usually attributed to a relapse of this disease and neuroradiological studies are not always performed. When done, the flnding of a new focal mass lesion is usually interpreted as a pseudotumoural plaque.
A 37-year-old man was admitted because of partial simple seizures and an enlarging intracranial mass. He had been diagnosed of MS eleven years earlier. A MRI study performed eight years before admission showed a large mass in the right frontal lobe which was thought to be a pseudotumoural plaque. Two years later, he developed simple partial motor seizures that were initially controlled with valproic acid. He remained well until three months before admission, when seizures reappeared with a poor response to valproic acid. A new MRI study showed an heterogeneus right frontal enlarging mass lesion. A primary neoplasm was suspected and a subtotal removal was performed. The pathological diagnosis was oligodendroglioma with a periferic demielinating area.
Atypical MRI lesions in a patient with MS must be carefully interpreted. Pseudotumoural plaques have been described both clinically and radiologically to be hardly distinguishable from a tumoural lesion and histological confirmation is often required. The association between MS and glioma is uncommon but it must be kept in mind when a mass lesion develops in a patient with MS.
La coexistencia de esclerosis múltiple (EM) y glioma es un hecho infrecuente. Se han descrito unos 30 casos de esta rara asociación, pero en sólo seis de ellos el tumor fue un oligodendroglioma u oligoastrocitoma. La aparición de nuevos síntomas neurológicos en un paciente con EM es atribuida habi-tualmente a un nuevo brote de la enfermedad sin que se realicen nuevos estudios de imagen en la mayoría de los casos. El hallazgo de una lesión focal con efecto masa en un paciente con EM suele ser interpretada como una placa pseudotumoral.
Presentamos el caso de un varón de 37 años con una historia de EM de 11 años de evolución que presenta crisis parciales simples de nueva aparición y una lesión expansiva frontal derecha. En una RM cerebral realizada 8 años antes, ya presentaba una lesión frontal derecha con discreto efecto de masa que se interpretó como una placa pseudot |
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ISSN: | 1130-1473 |
DOI: | 10.1016/S1130-1473(04)70473-X |