Results 41 to 50 of about 31,139 (212)

Understanding Further the Phenotypic Spectrum of Central Nervous System Inflammatory Demyelinating Disorders Using Unsupervised Clustering

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Central nervous system (CNS) inflammatory demyelinating syndromes, including multiple sclerosis (MS), aquaporin‐4 antibody–positive neuromyelitis optica spectrum disorder (AQP4 + NMOSD), and myelin oligodendrocyte glycoprotein (MOG) antibody–associated disease (MOGAD), occasionally overlap.
Bade Gulec, Elif Everest, Melih Tutuncu, Ugur Bilge, Sabahattin Saip, Ugur Uygunoglu, Aksel Siva   +6 more
wiley   +1 more source

Paraneoplastic neurological syndrome: focus on the involvement of the peripheral nervous system [PDF]

Саратовский научно-медицинский журнал, 2017
The information about epidemiology, pathogenesis and clinical heterogeneity of paraneoplastic neurological syndrome is summarized and based on Russian and foreign literature. The main attention is devoted to the affection of peripheral nervous systems in
Sitkali I.V., Kolokolov O.V.
doaj  

Hodgkin's lymphoma‐associated vanishing bile duct syndrome successfully treated with radiation as a bridge to chemotherapy

Precision Radiation Oncology, 2021
Vanishing bile duct syndrome is a paraneoplastic manifestation of Hodgkin's lymphoma that often proves fatal. Treatment of the underlying lymphoma with chemotherapy is a priority, and liver dysfunction is frequently prohibitive.
Maryam Ebadi, Jeffrey Olson, Justin Bateman, Damien Mathew, Jianling Yuan, Armin Rashidi   +5 more
doaj   +1 more source

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar, Jeremy Johnson, Susanne Watkins, Eoin Mulroy   +3 more
wiley   +1 more source

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro, Shiwen Koay, Gordon T. Ingle, Patricia McNamara, Laura Watson, Fion Bremner, Valeria Iodice   +6 more
wiley   +1 more source

Sweet′s syndrome with multiple myeloma

Journal of Applied Hematology, 2014
We are reporting a case of 70-yr-old gentleman who presented to dermatology clinic with painful red rash which was confirmed to be a sweet′s syndrome by biopsy . Further work up showed IgA myeloma. The patient showed good response to systemic and topical
Khalid Alsaleh
doaj   +1 more source

Autoimmune Encephalitis in Acute Care—Pathology, Diagnosis, and Management

Advanced Science, EarlyView.
ABSTRACT Autoimmune encephalitis (AE) is characterized by immune‐mediated inflammation of the brain parenchyma, presenting with various neurological syndromes, including but not limited to seizures, altered consciousness, neuropsychiatric symptoms, and movement disorders.
Suneesh Thilak, David Okoh, William Scotton, Shanika Samarasekera, Vikram Patil, Suresh Renukappa, Andrew Macduff, Subashini Suresh, Rajeev Krishnadas, Tonny Veenith   +9 more
wiley   +1 more source

Autoimmune encephalitis in psychiatric institutions: current perspectives

Neuropsychiatric Disease and Treatment, 2016
Chloe Bost,1–3 Olivier Pascual,2,3 Jérôme Honnorat1–3 1French Reference Center of Paraneoplastic Neurological Syndrome, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France; 2Synatac Team ...
Bost C, Pascual O, Honnorat J
doaj  

Cholestatic Jaundice as a Paraneoplastic Manifestation of Prostate Cancer

Case Reports in Urology, 2013
Paraneoplastic syndrome associated with prostate cancer is extremely rare. We report a patient who presented with cholestatic jaundice without biliary duct obstruction, hepatic involvement, or infection. After a few detailed examinations, prostate cancer
Tomomi Kuramoto, Hiroya Senzaki, Hiroyuki Koike, Kenji Yamagiwa, Shinobu Tamura, Tokuzou Fujimoto, Takeshi Inagaki   +6 more
doaj   +1 more source

Paraneoplastic neurologic syndromes

Annals of Oncology, 1995
Paraneoplastic neurologic syndromes (PNS) are remote, nonmetastatic complications of systemic cancer. Clinically they are characterized by subacute, progressive neurologic deficits that usually result in profound disability and eventually death. PNS may be present as long as 2 to 4 years before diagnosis of the associated tumor, but it can develop ...
Bauer J, Kuntzer T, Leyvraz S
openaire   +3 more sources