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1.
Cleve Clin J Med ; 90(7): 439-447, 2023 07 03.
Artigo em Inglês | MEDLINE | ID: mdl-37400156

RESUMO

Postural orthostatic tachycardia syndrome (POTS)-sustained tachycardia upon standing without orthostatic hypotension-can be diagnosed clinically without an extensive diagnostic evaluation unless certain atypical features suggest an alternative diagnosis. A unifying pathophysiologic mechanism has not been identified, although several have been proposed. Similarities between POTS and various autoimmune disorders suggest an immune mechanism in a subset of patients. However, no causative antibody has been identified, and associated antibodies are rarely clinically relevant. Moreover, immunotherapies are not currently recommended for POTS, although clinical trials are underway to clarify their utility.


Assuntos
Doenças Autoimunes , Síndrome da Taquicardia Postural Ortostática , Humanos , Síndrome da Taquicardia Postural Ortostática/diagnóstico , Síndrome da Taquicardia Postural Ortostática/terapia , Síndrome da Taquicardia Postural Ortostática/etiologia , Autoimunidade , Doenças Autoimunes/complicações , Frequência Cardíaca/fisiologia
2.
J Neuroimmunol ; 361: 577743, 2021 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-34695769

RESUMO

We present a patient with positive medium titer MOG-IgG and progressive neurological decline whose clinical and radiological phenotype were not consistent with a MOG-IgG associated disorder and ultimately received a diagnosis of glioblastoma after brain biopsy and died 4 weeks later. This represents an important topic with a high frequency of MOG-IgG testing in clinical practice. Due to this there are increasing reports of MOG-IgG positivity in atypical clinical phenotypes, raising the possibility of false positives, which can have important implications. It is important to highlight that judicious clinical evaluation is needed when interpreting MOG-IgG results in atypical settings.


Assuntos
Anticorpos Antineoplásicos/sangue , Autoanticorpos/sangue , Autoantígenos/imunologia , Neoplasias Encefálicas/imunologia , Erros de Diagnóstico , Glioblastoma/imunologia , Imunoglobulina G/sangue , Glicoproteína Mielina-Oligodendrócito/imunologia , Adulto , Autoanticorpos/imunologia , Biópsia , Neoplasias Encefálicas/sangue , Neoplasias Encefálicas/diagnóstico por imagem , Diagnóstico Tardio , Paralisia Facial/etiologia , Reações Falso-Positivas , Feminino , Transtornos Neurológicos da Marcha/etiologia , Glioblastoma/sangue , Glioblastoma/diagnóstico por imagem , Humanos , Imunoglobulina G/imunologia , Imageamento por Ressonância Magnética , Espectroscopia de Ressonância Magnética , Neuroimagem , Paresia/etiologia , Tomografia por Emissão de Pósitrons , Vertigem/etiologia , Transtornos da Visão/etiologia
3.
Muscle Nerve ; 61(5): 595-599, 2020 05.
Artigo em Inglês | MEDLINE | ID: mdl-32034782

RESUMO

BACKGROUND: We aimed to evaluate the significance of electromyographic findings in the intrinsic foot muscles (IFMs) of patients with skin biopsy proven small fiber neuropathy (SFN). METHODS: This was a single-center retrospective analysis of patients who underwent skin biopsy for intra-epidermal nerve fiber density (IENFD) measurement and electrodiagnostic (EDX) study for evaluation of polyneuropathy. RESULTS: A total of 1416 patents with normal lower extremity EDX studies proximal to the foot were included. Active denervation was seen in 16.1% of IFMs in patients with skin biopsy proven SFN and 4.1% of patients without SFN (P < .0001). Reinnervation changes without active denervation were observed in 30.4% of SFN patients and 23.8% of patients without SFN (P = .01). IENFD was lower in SFN patients with active denervation in IFMs than without (P < .0001). CONCLUSIONS: Evaluation of active denervation in the IFMs can reveal large fiber dysfunction in SFN patients with otherwise normal routine EDX findings.


Assuntos
Pé/inervação , Músculo Esquelético/inervação , Condução Nervosa/fisiologia , Neuropatia de Pequenas Fibras/fisiopatologia , Nervo Sural/fisiopatologia , Potenciais de Ação , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Eletrodiagnóstico , Eletromiografia , Epiderme/patologia , Feminino , Pé/fisiopatologia , Humanos , Masculino , Pessoa de Meia-Idade , Músculo Esquelético/fisiopatologia , Fibras Nervosas/patologia , Estudos Retrospectivos , Neuropatia de Pequenas Fibras/patologia , Coxa da Perna , Adulto Jovem
4.
Muscle Nerve ; 60(4): 376-381, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31348533

RESUMO

INTRODUCTION: Little is published on the prognosis of small fiber neuropathy (SFN). METHODS: A retrospective analysis of 101 patients with biopsy proven SFN. RESULTS: Study participants included 87 patients with length-dependent SFN and 14 patients with non-length-dependent SFN. The average duration of symptoms was 3.2 years prior to SFN diagnosis, and the average follow-up duration after diagnosis was 6.2 years. Neuropathic pain was present in 98% of patients and in 84.2% of patients at the final visit. The average total number of pain medications ever used was 4.4 per patient. Signs of autonomic dysfunction were initially present in 24.8% of patients, but improved in most. Large fiber involvement was seen in 11.9% of patients. Small fiber neuropathy affected employment and ambulation status in 5.3% and 6.3% of patients, respectively. DISCUSSION: Small fiber neuropathy tends to be stable and rarely affects ambulation and employment status. Effective pain control remains a challenge.


Assuntos
Doenças do Sistema Nervoso Autônomo/fisiopatologia , Emprego , Limitação da Mobilidade , Neuralgia/fisiopatologia , Neuropatia de Pequenas Fibras/fisiopatologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Analgésicos/uso terapêutico , Doenças do Sistema Nervoso Autônomo/etiologia , Biópsia , Feminino , Seguimentos , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Neuralgia/tratamento farmacológico , Neuralgia/etiologia , Prognóstico , Estudos Retrospectivos , Neuropatia de Pequenas Fibras/complicações , Neuropatia de Pequenas Fibras/patologia , Adulto Jovem
5.
Muscle Nerve ; 49(4): 564-9, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23893404

RESUMO

INTRODUCTION: Polyneuropathy evaluation in older patients is often challenging due to conflicting data regarding normative values for peripheral nerve testing. METHODS: We characterized the results of sural nerve conduction studies, intraepidermal nerve fiber density (IENFD), and quantitative sudomotor axon reflex testing (QSART) in a prospective study of 50 healthy subjects aged ≥60 years. RESULTS: Of the 50 subjects, 48 (96%) had an obtainable sural sensory nerve action potential (SNAP). Using quantile regression, we estimated the lower limit of normal (LLN) for sural amplitudes to be 3 µV for patients 60-70 years, 1 µV for those 70-74 years, and <1 µV (absent) for those ≥75 years of age. IENFD and QSART volume were reduced with advancing age, although IENFD was lower in men and QSART volume was lower in women. CONCLUSIONS: We propose that an absent sural SNAP in patients up to 75 years of age should be considered abnormal. Our findings also support age- and gender-stratified normative data for IENFD and QSART.


Assuntos
Potenciais de Ação/fisiologia , Axônios/fisiologia , Epiderme/inervação , Epiderme/fisiologia , Reflexo/fisiologia , Nervo Sural/fisiologia , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Eletromiografia/métodos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fibras Nervosas/fisiologia , Estudos Prospectivos
6.
J Stroke Cerebrovasc Dis ; 18(6): 428-34, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19900644

RESUMO

Tentorial dural arteriovenous fistulas (TDAVFs) draining into the spinal venous system are rare lesions. The clinical presentation can be devastating and the diagnosis delayed because of the initial nonspecific imaging and laboratory findings. We report a case of a 20-year-old woman with a rapidly progressive myelopathy, who was found to have a left TDAVF, fed by a single arterial feeder with drainage into the perimedullary venous system. The fistula was surgically clipped. The patient showed neurologic improvement at her 3-month follow-up but still had significant weakness of all 4 extremities. Early diagnosis is key as the neurologic symptoms are reversible with appropriate treatment. We review the relevant literature, imaging characteristics, and treatment modalities for TDAVF.


Assuntos
Malformações Vasculares do Sistema Nervoso Central/complicações , Quadriplegia/etiologia , Edema Encefálico/etiologia , Malformações Vasculares do Sistema Nervoso Central/diagnóstico , Malformações Vasculares do Sistema Nervoso Central/fisiopatologia , Malformações Vasculares do Sistema Nervoso Central/cirurgia , Angiografia Cerebral , Diagnóstico Precoce , Feminino , Hemodinâmica , Humanos , Imageamento por Ressonância Magnética , Exame Neurológico , Quadriplegia/diagnóstico , Quadriplegia/fisiopatologia , Quadriplegia/cirurgia , Recuperação de Função Fisiológica , Resultado do Tratamento , Procedimentos Cirúrgicos Vasculares , Adulto Jovem
7.
Am J Obstet Gynecol ; 201(5): 531.e1-7, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19761997

RESUMO

OBJECTIVE: The purpose of this study was to determine the incidence and time course of postoperative neuropathy resulting from gynecologic surgery. STUDY DESIGN: A single cohort of 616 female patients undergoing elective gynecologic surgery for benign or malignant conditions at a tertiary care academic medical center underwent a postoperative neurologic evaluation to identify postoperative neuropathy of the lower extremities. RESULTS: Fourteen peripheral nerve injuries were observed in 11 patients, making the overall incidence of postoperative neuropathy 1.8% (95% confidence interval, 1.0-3.2). Injury to the lateral femoral cutaneous (5), femoral (5), common fibular (1), ilioinguinal/iliohypogastric (1), saphenous (1), and genitofemoral (1) nerves were detected. Complete resolution of neuropathic symptoms occurred in all but 1 patient (91%). Median time to resolution of symptoms was 31.5 days (range, 1 day to 6 months). CONCLUSION: The incidence of lower extremity neuropathy attributable to gynecologic operations is low, and these neuropathies resolve in the great majority of cases.


Assuntos
Procedimentos Cirúrgicos em Ginecologia/efeitos adversos , Traumatismos do Sistema Nervoso/epidemiologia , Traumatismos do Sistema Nervoso/etiologia , Feminino , Humanos , Incidência , Pessoa de Meia-Idade , Pelve , Estudos Prospectivos
8.
Neurol Clin ; 25(2): 373-85, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17445734

RESUMO

Cervical radiculopathy is a condition encountered commonly in the evaluation of neck pain that may result in significant discomfort and functional deficits. Although the long-term prognosis of this condition is favorable, a standardized approach to therapy is important to minimize unnecessary tests and identify patients who require more urgent intervention. Patient education, pain control, and physical therapy are the first line of therapy. Patients who have protracted pain or significant functional deficits may require a more thorough evaluation, including imaging, electrodiagnostic testing, and, possibly, surgical referral. This article outlines the basic clinical, diagnostic, and therapy considerations in the evaluation of cervical radiculopathy.


Assuntos
Radiculopatia/fisiopatologia , Vértebras Cervicais/inervação , Vértebras Cervicais/fisiopatologia , Humanos , Incidência , Prevalência , Radiculopatia/epidemiologia , Radiculopatia/etiologia , Raízes Nervosas Espinhais/fisiopatologia
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