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Progressive multifocal leukoencephalopathy: MRI findings in HIV-infected patients are closer to rituximab- than natalizumab-associated PML

OBJECTIVES: To compare brain MRI findings in progressive multifocal leukoencephalopathy (PML) associated to rituximab and natalizumab treatments and HIV infection. MATERIALS AND METHODS: In this retrospective, multicentric study, we analyzed brain MRI exams from 72 patients diagnosed with definite P...

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Detalles Bibliográficos
Autores principales: Alleg, Manel, Solis, Morgane, Baloglu, Seyyid, Cotton, François, Kerschen, Philippe, Bourre, Bertrand, Ahle, Guido, Pruvo, Jean-Pierre, Leclerc, Xavier, Vermersch, Patrick, Papeix, Caroline, Maillart, Élisabeth, Houillier, Caroline, Chabrot, Cécile Moluçon, Claise, Béatrice, Malak, Sandra, Martin-Blondel, Guillaume, Bonneville, Fabrice, Caulier, Alexis, Marolleau, Jean-Pierre, Bonnefoy, Jérôme Tamburini, Agape, Philippe, Kennel, Céline, Roussel, Xavier, Chauchet, Adrien, De Seze, Jérôme, Fafi-Kremer, Samira, Kremer, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644389/
https://www.ncbi.nlm.nih.gov/pubmed/33155106
http://dx.doi.org/10.1007/s00330-020-07362-y
Descripción
Sumario:OBJECTIVES: To compare brain MRI findings in progressive multifocal leukoencephalopathy (PML) associated to rituximab and natalizumab treatments and HIV infection. MATERIALS AND METHODS: In this retrospective, multicentric study, we analyzed brain MRI exams from 72 patients diagnosed with definite PML: 32 after natalizumab treatment, 20 after rituximab treatment, and 20 HIV patients. We compared T2- or FLAIR-weighted images, diffusion-weighted images, T2*-weighted images, and contrast enhancement features, as well as lesion distribution, especially gray matter involvement. RESULTS: The three PML entities affect U-fibers associated with low signal intensities on T2*-weighted sequences. Natalizumab-associated PML showed a punctuate microcystic appearance in or in the vicinity of the main PML lesions, a potential involvement of the cortex, and contrast enhancement. HIV and rituximab-associated PML showed only mild contrast enhancement, punctuate appearance, and cortical involvement. The CD4/CD8 ratio showed a trend to be higher in the natalizumab group, possibly mirroring a more efficient immune response. CONCLUSION: Imaging features of rituximab-associated PML are different from those of natalizumab-associated PML and are closer to those observed in HIV-associated PML. KEY POINTS: • Nowadays, PML is emerging as a complication of new effective therapies based on monoclonal antibodies. • Natalizumab-associated PML shows more inflammatory signs, a perivascular distribution “the milky way,” and more cortex involvement than rituximab- and HIV-associated PML. • MRI differences are probably related to higher levels of immunosuppression in HIV patients and those under rituximab therapy.