7 results match your criteria: "Centre de Référence Français des Syndromes Neurologiques Paranéoplasiques et des Encéphalites Auto-immunes[Affiliation]"

Article Synopsis
  • Mononeuritis multiplex is a rare but severe side effect associated with immune checkpoint inhibitors, particularly noted in three patients with mesothelioma in a French study.
  • The study involved three elderly male patients who exhibited severe neurological symptoms and were diagnosed with mononeuritis multiplex after receiving treatment with nivolumab and ipilimumab.
  • All patients were treated with corticosteroids, resulting in improvements, but one patient required additional therapy (rituximab and cyclophosphamide) after symptom recurrence upon tapering steroids.
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Advances in treatments of patients with classical and emergent neurological toxicities of anticancer agents.

Rev Neurol (Paris)

June 2023

Service de Neurologie, Hôpital d'Instruction des Armées Percy, Service de Santé des Armées, Clamart, France; UMR 9010 Centre Borelli, Université Paris-Saclay, École Normale Supérieure Paris-Saclay, CNRS, Service de Santé des Armées, Université Paris Cité, Inserm, Saclay, France; OncoNeuroTox Group: Center for Patients with Neurological Complications of Oncologic Treatments, Hôpitaux Universitaires Pitié-Salpêtrière - Charles-Foix et Hôpital d'Instruction des Armées Percy, Paris, France; École du Val-de-Grâce, Service de Santé des Armées, Paris, France. Electronic address:

The neurotoxicity associated to the anticancer treatments has received a growing body of interest in the recent years. The development of innovating therapies over the last 20years has led to the emergence of new toxicities. Their diagnosis and management can be challenging in the clinical practice and further research is warranted to improve the understanding of their pathogenic mechanisms.

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[Autoimmune encephalitis : an update].

Rev Prat

January 2022

Centre français de référence des syndromes neurologiques paranéoplasiques et des encéphalites auto-immunes, Hospices civils de Lyon ; Hôpital neurologique de Bron ; Hôpital neurologique de Lyon, France Équipe Synaptopathies et auto-anticorps (SynatAc), institut NeuroMyoGène, Inserm U1217/CNRS UMR 5310, université Claude-Bernard, Lyon, France.

Autoimmune encephalitis: an update. Autoimmune encephalitis (AE) are rare autoimmune disorders of the central nervous system associated with anti-neuron antibodies. Patients classically present with anterograde amnesia, temporal lobe seizures, and/or behavioral changes, along with a variety of possible other symptoms, depending on the autoantibody.

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Glial Fibrillary Acidic Protein Autoimmunity: A French Cohort Study.

Neurology

February 2022

From Service de Neurologie, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Inflammation, and Centre de Référence des Maladies Inflammatoires Rares du Cerveau et de la Moelle (A.G.-D., R.M.), Service d'Imagerie Médicale (R.A.), and Centre de Référence des Syndromes Neurologiques Paranéoplasiques et Encéphalites Auto-immunes (V.R., B.J., S.M.-C., A.V., G.P., J.H.), Hôpital Neurologique Pierre Wertheimer, and Service de Neurologie Pédiatrique, Hôpital Femme Mère Enfant (C.F.), Hospices Civils de Lyon, Lyon/Bron; Institut NeuroMyoGène (V.R., B.J., S.M.-C., A.V., G.P., J.H.), INSERM 1217 et CNRS UMR5310; Université Claude Bernard Lyon 1 (V.R., B.J., S.M.-C., A.V., G.P., J.H.), Faculté de Médecine Lyon Est; Centre de Recherche en Neurosciences de Lyon (A.R., R.M.), INSERM 1028 et CNRS UMR5292, France; Stanford University Center for Sleep Sciences and Medicine (A.A.), Palo Alto, CA; Service de Neurologie Cognitive, Épilepsie, Sommeil et Mouvements Anormaux (M. Benaiteau) and Service de Neurologie Inflammatoire et Neuro-oncologie (F.R., J.C.), Hôpital Pierre-Paul Riquet, Hôpitaux de Toulouse; Service de Neuropédiatrie (K.D.), Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, Le Kremlin-Bicêtre; Service de Neurologie (T.d.B.), Hôpital Delafontaine, Centre Hospitalier de Saint-Denis; Service de Neurologie, Hôpital de Hautepierre (L.K.), Hôpitaux Universitaires de Strasbourg; Service de Neurologie (P.K.), Centre Hospitalier de Luxembourg; Service de Neurologie (F.S.) and Service de Médecine Interne (B.B.), Hôpitaux Civils de Colmar; Unité INSERM U-1118 (F.S.), Faculté de Médecine, Université de Strasbourg; Service de Médecine Interne (R.G.), Hôpital d'Instruction des Armées Legouest, Metz; Service de Neurologie (J.B.) and Service de Médecine Interne et Immunologie Clinique (A.B.), Centre Hospitalier Régional Universitaire de Tours; Service de Neurologie et Maladies Neuromusculaires (F.D.), Groupe Hospitalier Pellegrin, Hôpitaux de Bordeaux; Service de Médecine Intensive et Réanimation (N.I.), Hôpital Saint André, Bordeaux; Service de Neurologie (E.-C.R.), Hôpital Sainte Musse, Centre Hospitalier Intercommunal de Toulon; Service de Neurologie (M.G.), Hôpital Emile Muller, Mulhouse; Service de Neurologie (A.D.), Centre Hospitalier de Perpignan; Pôle Cardio-vasculaire et Métabolique (J.L.D.), Centre Hospitalier de Cayenne; Service de Neurologie (L.H.), Hôpital Central, CHRU Nancy; Service de Neurologie (A.-L.K.), CHU de Saint-Etienne, Saint-Priest-en-Jarez; Service de Neuropédiatrie (M.P.), Site Mère Enfant, CHU Martinique, Fort-de-France; Service de Neurologie (E.C.), CHU Gabriel-Montpied, CHU de Clermont-Ferrand; Service de Neurologie (A.L.), Hôpital d'Instruction des Armées Clermont-Tonnerre, Brest; Service de Neurologie (E.M.), Hôpital Fondation Adolphe de Rothschild, Paris; Service de Neurologie et Laboratoire de Neurosciences Fonctionnelles et Pathologies (D.A.), Centre Hospitalier Universitaire d'Amiens et Université de Picardie Jules Verne, Amiens; Service de Neurologie (P.D.), Hôpital Laënnec, Centre Hospitalier de Cornouaille, Quimper; Service de Neurologie (G.M.), Centre Hospitalier Universitaire de La Réunion, Saint Pierre; Service de Neurologie (C.D.), Hôpital Roger Salengro, Centre Hospitalier Universitaire de Lille; Service de Neurologie (V.B.), Hôpital Pasteur 2, Centre Hospitalier Universitaire de Nice; Service de Médecine Interne et Maladies Infectieuses (Q.B.), Centre Hospitalier d'Angoulême; Service de Neurologie (I.G.-C.) and Service de Réanimation (G.R.), Centre Hospitalier de Saint-Brieuc; Service de Médecine Polyvalente et de Médecine Interne (D.M.-T.), Centre Hospitalier Le Mans; Service de Neurologie (M. Bonnan), Centre Hospitalier de Pau; and Service de Neurologie/UNV (T.T.), Centre Hospitalier de Saintonge, Saintes, France.

Background And Objectives: To report the clinical, biological, and imaging features and clinical course of a French cohort of patients with glial fibrillary acidic protein (GFAP) autoantibodies.

Methods: We retrospectively included all patients who tested positive for GFAP antibodies in the CSF by immunohistochemistry and confirmed by cell-based assay using cells expressing human GFAPα since 2017 from 2 French referral centers.

Results: We identified 46 patients with GFAP antibodies.

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Neurological diseases of unknown etiology: Brain-biopsy diagnostic yields and safety.

Eur J Intern Med

October 2020

Sorbonne Université, UPMC Univ. Paris 06, F-75005, Paris, France; AP-HP, Hôpitaux Universitaires La Pitié-Salpêtrière - Charles Foix, Institut E3M, Service de Médecine Interne 2, Centre de Référence National Lupus Systémique, Syndrome des Anticorps Anti-Phospholipides et Autres Maladies Auto-Immunes Systémiques Rares, F-75013, Paris, France; AP-HP, Hôpitaux Universitaires La Pitié-Salpêtrière - Charles Foix, Institut de Cardiométabolisme et Nutrition (ICAN), Service de Médecine Intensive-Réanimation, F-75013, Paris, France.

Article Synopsis
  • This study looked at patients with brain problems that doctors didn't know the cause of and checked the safety and usefulness of a test called a brain biopsy.
  • Out of 178 biopsies done, about 71% of the patients got a clear diagnosis, and 75% experienced treatment changes afterward.
  • The study found that while complications from the biopsy were rare, certain conditions like low platelet count could make these problems more likely, suggesting that it might be best to do biopsies earlier when needed.
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Background: Paraneoplastic syndromes (PNS) are autoimmune disorders specifically associated with cancer. There are few data on anti-PD-1 or anti-PD-L1 immunotherapy in patients with a PNS. Our objective was to describe the outcome for patients with a pre-existing or newly diagnosed PNS following the initiation of anti-PD-1 or anti-PD-L1 immunotherapy.

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