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1.
Arch Soc Esp Oftalmol (Engl Ed) ; 97(3): 168-171, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35248399

RESUMO

Primary central nervous system lymphoma is one of the most infrequent brain tumours, accounting for 3% of primary central nervous system neoplasms. In addition to its low prevalence, clinical presentation is usually nonspecific, leading to diagnostic delay. Intraocular involvement occurs in 15% of cases, and disease onset in this location is even rarer. We present a case of a patient with intermediate uveitis as the first clinical manifestation of this neoplasm.


Assuntos
Neoplasias Encefálicas , Linfoma , Uveíte , Neoplasias Encefálicas/diagnóstico por imagem , Sistema Nervoso Central/patologia , Diagnóstico Tardio , Humanos , Linfoma/diagnóstico por imagem , Uveíte/diagnóstico
2.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33640210

RESUMO

Primary central nervous system lymphoma is one of the most infrequent brain tumours, accounting for 3% of primary central nervous system neoplasms. In addition to its low prevalence, clinical presentation is usually nonspecific, leading to diagnostic delay. Intraocular involvement occurs in 15% of cases, and disease onset in this location is even rarer. We present a case of a patient with intermediate uveitis as the first clinical manifestation of this neoplasm.

3.
Mult Scler Relat Disord ; 39: 101892, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31846866

RESUMO

BACKGROUND: Although solid information on the natural history of primary progressive multiple sclerosis (PPMS) is available, evidence regarding impact of disease activity on PPMS progression remains controversial. OBJECTIVE: To describe the clinical characteristics, presence or absence of MRI activity, and natural history of a PPMS cohort from two referral centers in Argentina and assess whether clinical and/or radiological disease activity correlated with disability worsening. METHODS: Retrospective study conducted at two MS clinics in Buenos Aires, Argentina, through comparative analysis of patients with and without evidence of disease activity. RESULTS: Clinical and/or radiologic activity was presented in 56 (31%) of 178 patients. When stratified by age at onset, we found that for every 10 years of increase in age at onset, risk of reaching EDSS scores of 4 and 6 increased by 26% and 31%, respectively (EDSS 4: HR 1.26, CI 95%: 1.06-1.50; EDSS 6: HR 1.31, CI 95%: 1.06-1.62). Patients who presented clinical exacerbations reached EDSS scores of 6, 7 and 8 faster than those without associated exacerbations (p = 0.009, p = 0.016 and p = 0.001, respectively). Likewise, patients who presented gadolinium-enhancing lesions during the course of disease reached EDSS scores of 7 earlier (p = 0.002). CONCLUSION: Older age at onset and presence of clinical and/or radiological disease activity correlated with accelerated disability progression in this cohort of PPMS patients.

4.
Rev Neurol ; 69(7): 301-302, 2019 Oct 01.
Artigo em Espanhol | MEDLINE | ID: mdl-31559629
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