Gliomatosis cerebri (brain tumor)
Two clinical cases
Keywords:
GLIOMA, BRAIN NEOPLASMSAbstract
Introduction: gliomatosis cerebri (GC) is a neoepithelium neoplastic disease affecting at least two lobes. Its clinical presentation is non-specific, imagenology and pathological anatomy studies being the main diagnostic pillars. The incidence of GC is low and average age of presentation is in the forties and fifties years of age.
Method: The study presents two clinical cases; the first one of which manifests as depressed consciousness associated to alterations in behavior, the second one manifesting as unsteady gait. In both cases diagnosis was based on magnetic resonance and pathological anatomy.
Results: both patients evidenced a two month survival rate subsequent to diagnosis, and no treatment was applied given the bad evolution of the disease.
Conclusions: GC is a low incidence neoplastic disease with varied forms of clinical presentation. Its diagnosis is based on two main pillars: imagenology and pathological anatomy studies. Associating chemotherapy (temozolomide) to the classic treatment of radiotherapy seems to result in higher response rates, although its impact on survival is still poor. Prognosis is bad, and survival rates range from 6 to 12 months.
References
(2) Jiménez Caballero PE, Mollejo Villanueva M, Marsal Alonso C. Gliomatosis cerebri: evolución a glioblastoma multiforme. Neurología 2007; 22(6):395-8.
(3) Rajz GG, Nass D, Talianski E, Pfeffer R, Spiegelmann R, Cohen ZR. Presentation patterns and outcome of gliomatosis cerebri. Oncol Lett 2012; 3(1):209-13.
(4) Porta Etessam J, Berbel García A, Martínez Salio A, Balsalobre Aznar J, Madero S, Ramos González A, et al. Gliomatosis Cerebri: RM, SPECT y estudio patológico. Rev Neurol 1999; 29(3):287-8.
(5) Narasimhaiah D, Miquel C, Verhamme E, Desclée P, Cosnard G, Godfraind C. IDH1 mutation, a genetic alteration associated with adult gliomatosis cerebri. Neuropathology 2012; 32(1):30-7.
(6) Bruna J, Velasco R. Gliomatosis cerebri. Neurología 2010; 25(10):143-7.
(7) Soffietti R, Rudà R, Laguzzi E, Buttolo A, Pace A, Carapella C, et al. Treatment of gliomatosis cerebri with temozolomide: a retrospective study of the AINO (Italian Association for Neuro- Oncology). J Clin Oncol 2007; 25(18 Suppl):2033.
(8) Santos-Lasaosa S, López-García E, Ríos C, Espada-Oliván F, Iñíguez-Martínez C, Mostacero-Miguel E, et al. Gliomatosis cerebral: presentación de tres casos y revisión de la literatura. Rev Neurol 2002; 34(3):248-52.
(9) Mena IX, Olivares DA, del Bruto OH, Leone-Stay G. Gliomatosis cerebri: clinico pathological and and neuroimaging characteristics, and the results of treatment with radiotherapy. Rev Neurol 2004; 31(2):101-6.
(10) Dresemann G. Temozolomide in malignant glioma. Onco Targets Ther 2010; 3:139-46.
(11) Preusser M, de Ribaupierre S, Wöhrer A, Erridge SC, Hegi M, Weller M, et al. Current concepts and management of glioblastoma. Ann Neurol 2011; 70(1):9-21.
(12) Herrlinger U, Schaefer N, Steinbach PJ, Weyerbrock A, Hau P, Goldbrunner R, et al. Bevacizumab, irinotecan, and radiotherapy versus standard temozolomide and radiotherapy in newly diagnosed, MGMT-nonmethylated glioblastoma patients: first results from the randomized multicenter GLARIUS trial. J Clin Oncol 2013; 31 (suppl. Abstr): LBA2000.