Results 61 to 70 of about 4,018 (183)

Definition and Consensus Diagnostic Criteria for Neurosarcoidosis: From the Neurosarcoidosis Consortium Consensus Group

open access: yes, 2018
IMPORTANCE The Neurosarcoidosis Consortium Consensus Group, an expert panel of physicians experienced in the management of patients with sarcoidosis and neurosarcoidosis, engaged in an iterative process to define neurosarcoidosis and develop a practical ...
Tavee, Jinny   +13 more
core   +1 more source

Diagnostic value of soluble Interleukin-2 receptor in patients suffering neurosarcoidosis: A systematic review

open access: yesJournal of Central Nervous System Disease
Background Neurosarcoidosis is an inflammatory granulomatous disease. Up to 25% of occult sarcoidosis affecting the nervous system are only detected by autopsy. In addition, in recent years the suspicion arose that the soluble Interleukin-2 Receptor (sIL-
Aditya Chanpura   +3 more
doaj   +1 more source

Rare Case of Spinal Neurosarcoidosis with Concomitant Epidural Lipomatosis

open access: yesCase Reports in Neurological Medicine, 2021
Introduction. Spinal neurosarcoidosis is a rare disease that can manifest as myelopathy, radiculopathy, or cauda equine syndrome. Spinal epidural lipomatosis is also a rare condition resulting from overgrowth of epidural fat tissue causing compressive ...
Nesreen Jaafar   +3 more
doaj   +1 more source

Intraosseous sarcoidosis imitating peri‐implantitis: A case study

open access: yesClinical Advances in Periodontics, Volume 16, Issue 2, Page 251-259, June 2026.
Abstract Background Sarcoidosis is a multisystem granulomatous disorder of unknown cause, typically affecting the lungs and lymph nodes, but it can also involve the eyes, skin, heart, bones, and other organs. The exact cause is unclear, but genetic factors and environmental triggers like infections, chemicals, or dust may play a role.
Magdalena Orlowska   +2 more
wiley   +1 more source

Cerebrospinal fluid CD4(+)/CD8(+)ratio in diagnosing neurosarcoidosis

open access: yes, 2020
Objective Neurosarcoidosis affects 5%-10% of patients with sarcoidosis. CD4(+)/CD8(+)ratio in bronchoalveolar lavage is included in diagnostic routine for pulmonary sarcoidosis.
Malmeström, Clas,   +2 more
core   +1 more source

Neurosarcoidosis

open access: yes, 2020
This is an illustrated guide to the clinical diagnosis of neurosarcoidosis. Sarcoidosis is a chronic systemic inflammatory disorder characterized by non-caseating granulomas.
Bryce Buchowicz, MD; Valérie Biousse, MD
core  

Neurosarcoidosis and MOG-associated Disease

open access: yes, 2022
Myelin oligodendrocyte glycoprotein (MOG) is a protein found on the surface of myelin, and anti-MOG antibodies can be elevated in demyelinating conditions such as multiple sclerosis, neuromyelitis optica spectrum disorder, or other MOG- associated ...
Sahar Noorani; Alden Gregston; Justin Bishop; Lauren Tardo; Melanie Truong-Le
core  

[Neurosarcoidosis--different manifestations]

open access: yes, 2010
We present six cases with different manifestations of neurosarcoidosis. There are no specific diagnostic tests for sarcoidosis. In the presented cases the diagnosis was made by histological proof of noncaseating granulomas.
Frederiksen, Jette, Magyari, Melinda
core   +1 more source

Application of the modified Zajicek criteria to diagnose probable spinal cord neurosarcoidosis

open access: yesClinical Case Reports, 2018
Key Clinical Message Neurosarcoidosis represents a significant diagnostic challenge, as clinical features overlap with other neuroinflammatory conditions, and biopsy of affected neuronal tissue is often high risk or not feasible.
Ceris Ifan Owen   +2 more
doaj   +1 more source

Neurolymphomatosis mimicking neurosarcoidosis: a case report

open access: yesJournal of Medical Case Reports, 2010
Introduction Both neurosarcoidosis and central nervous system lymphoma can be very difficult to diagnose. We describe the case of a patient in whom neurosarcoidosis was strongly suspected, but who was eventually found to have lymphoma.
Scolding Neil J, Santos Ernestina
doaj   +1 more source

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