Results 41 to 50 of about 3,766 (196)

Unusual presentation of sarcoidosis: solitary intracranial mass lesion mimicking an intracranial neoplasm: a case report

open access: yesThe Pan African Medical Journal, 2014
Sarcoidosis is a multisystem disease of unknown cause and with a worldwide distribution. Involvement of the central nervous system occurs in a relatively small number of patients with sarcoidosis.
Amen Ghozzi   +7 more
doaj   +1 more source

Neurosarcoidosis Affecting the Spinal Cord

open access: yes, 2011
Sarcoidosis is a chronic inflammatory disease that involves multiple systems. Complications in the nervous system are rare, especially in Asia. This report describes an unusual case of neurosarcoidosis affecting the spinal cord and other systems in a 53 ...
蔡忠芬;葉炳强;楊智超   +1 more
core   +1 more source

Neurosarcoidosis in a young male presenting with intractable migraines, blurry vision, and other nonspecific neurological symptoms case report

open access: yesBulletin of the National Research Centre, 2023
Background Neurosarcoidosis can have various neurological outcomes and presentations. It is an uncommon diagnosis, especially in young Caucasian males presenting with predominantly migraine headaches. Case presentation A Caucasian male in his 20s with no
Jack Jnani
doaj   +1 more source

Neurosarcoidosis, Coccidioidomycosis, or Both!

open access: yes, 2023
Amir Akhavanrezayat,1 Wataru Matsumiya,1,2 Prapatsorn Ongpalakorn,1 Hashem H Ghoraba,1 Chris Or,1 Hassan Khojasteh Jafari,1 Gunay Uludag Kirimli,1 Cigdem Yasar,1 Ngoc Trong Tuong Than,1 Irmak Karaca,1 Moosa Zaidi,1 Azadeh Mobasserian,1 Negin Yavari,1 ...
Than NTT   +16 more
core  

Unusual presentation of a skull base mass lesion in sarcoidosis mimicking malignant neoplasm: a case report

open access: yesBMC Neurology, 2018
Background Sarcoidosis is a multi-organ disease of unknown etiology characterised by the presence of epithelioid granulomas, without caseous necrosis. Systemic sarcoidosis is rare among children, while neurosarcoidosis in children is even rarer whether ...
Katsunori Shijo   +7 more
doaj   +1 more source

Isolated Neurosarcoidosis Presenting as Chronic Progressive Pachymeningitis

open access: yes, 2023
Neurologic manifestations of sarcoidosis are rare, and even rarer still are cases of isolated neurosarcoidosis. The clinical presentation of isolated neurosarcoidosis can be highly variable, and diagnosis is particularly challenging, the gold standard ...
Joshua Abata   +3 more
core   +1 more source

Infliximab treatment in pathology-confirmed neurosarcoidosis [PDF]

open access: yes, 2020
OBJECTIVE: To assess the efficacy and risks of treatment with infliximab (anti-tumor necrosis factor alpha) in pathology-confirmed neurosarcoidosis. METHODS: In a retrospective study in 2 tertiary referral centers in the Netherlands, we analyzed clinical
Siepman, T.A.M. (Theodora)   +13 more
core   +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

A Case of Neurosarcoidosis-Induced Syndrome of Inappropriate Secretion of Antidiuretic Hormone Diagnosed with Neuroendoscopy

open access: yesCase Reports in Medicine, 2018
We treated a patient with neurosarcoidosis, which caused the syndrome of inappropriate secretion of antidiuretic hormone (SIADH), in whom diagnosis was performed using neuroendoscopy.
Shiko Gen   +6 more
doaj   +1 more source

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi   +6 more
wiley   +1 more source

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