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1.
Neurology ; 103(3): e209708, 2024 Aug 13.
Artigo em Inglês | MEDLINE | ID: mdl-38991193

RESUMO

The clinical assessment of patients with proximal muscle weakness represents a frequent yet intricate challenge. We present the case of a 60-year-old woman who experienced a progressive, symmetrical weakness in proximal limbs and bulbar muscles over 6 months. Notable clinical findings included bilateral ophthalmoparesis; widespread muscle atrophy; and pronounced weakness in craniobulbar, cervical, and proximal muscles, more severe than in distal ones. We elucidate a methodical diagnostic approach, focusing on constructing a comprehensive differential diagnosis and identifying potential causes of proximal muscle weakness. Special emphasis is placed on exploring the etiologies in cases presenting with both progressive muscle weakness and ophthalmoparesis. We further describe the role of muscle biopsy results and their integration with genetic testing outcomes.


Assuntos
Debilidade Muscular , Oftalmoplegia , Humanos , Feminino , Pessoa de Meia-Idade , Debilidade Muscular/etiologia , Debilidade Muscular/diagnóstico , Oftalmoplegia/diagnóstico , Raciocínio Clínico , Diagnóstico Diferencial , Progressão da Doença
2.
Muscle Nerve ; 63(3): 357-364, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33280141

RESUMO

BACKGROUND: Patients with myasthenia gravis (MG) may be particularly vulnerable during the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic due to risk of worsening disease during infection, potential adverse impacts of coronavirus disease 2019 (COVID-19) treatments on neuromuscular transmission, and a limited ability to fight off infection related to immunosuppressive treatments. Our goal is to understand how patients are experiencing the COVID-19 pandemic, including where they receive relevant information, how it has affected medical care, and what measures they use to protect themselves. METHODS: This is a prospective online survey study at large academic practice. All patients with a neuromuscular junction disorder diagnosis code in the Duke Health System were invited to participate. RESULTS: One thousand eight hundred and forty eight patients were approached to participate and 75 completed the survey between 16 April 2020 and 28 May 2020. The most frequently used information sources were non-presidential federal government (75%), state government (57%), local healthcare provider (37%), and television news (36%). Non-presidential federal government (80%), local healthcare providers (55%), state government (33%), and patient support organizations (29%) were considered the most trusted information sources. Thirty-three (44%) of survey responders had attended a telemedicine visit. Patients were taking recommended precautions during the pandemic and remained very concerned (69%) about COVID-19. Generalized Anxiety Disorder-7 scores were moderate-severe in 20% of responders. CONCLUSIONS: Healthcare providers, the government, and patient organizations play a critical role in communicating with the MG patient community. Use of targeted messaging strategies by these groups to convey accurate information may increase effectiveness and lead to more informed patients with reduced anxiety.


Assuntos
COVID-19 , Conhecimentos, Atitudes e Prática em Saúde , Miastenia Gravis , Idoso , Estudos de Coortes , Governo Federal , Feminino , Desinfecção das Mãos , Pessoal de Saúde , Humanos , Masculino , Máscaras , Pessoa de Meia-Idade , Questionário de Saúde do Paciente , Distanciamento Físico , Estudos Prospectivos , SARS-CoV-2 , Governo Estadual , Inquéritos e Questionários , Telemedicina , Televisão , Estados Unidos
3.
Neuromuscul Disord ; 27(3): 266-268, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28109638

RESUMO

Immune checkpoint molecules are potent regulators of immunologic homeostasis that prevent the development of autoimmunity while maintaining self-tolerance. Inhibitors of immune checkpoint molecules are used as immunotherapy in the treatment of melanoma and different types of refractory cancer, and can trigger various autoimmune complications including myositis and myasthenia gravis. We describe a case of generalized myasthenia gravis induced by pembrolizumab and review 11 other cases. Five patients also had elevated serum CK levels ranging from 1200 to 8729 IU/L, and biopsy showed myositis in one. Severity was highly variable as symptoms normalized spontaneously in one patient, but three others developed myasthenic crisis (including two with fatal outcomes). Steroids have been recommended as a preferred treatment of autoimmune complications of immune-checkpoint inhibitors. Myasthenia gravis should be considered when weakness, diplopia or bulbar symptoms are seen after treatment with immune checkpoint inhibitors, and additional studies are needed to characterize association with hyperCKemia.


Assuntos
Anticorpos Monoclonais Humanizados/efeitos adversos , Antineoplásicos Imunológicos/efeitos adversos , Creatina Quinase/sangue , Miastenia Gravis/induzido quimicamente , Idoso , Feminino , Humanos , Miastenia Gravis/sangue , Miastenia Gravis/fisiopatologia
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