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Related Concept Videos

Myocarditis II: Clinical Features and Diagnostic Tests01:27

Myocarditis II: Clinical Features and Diagnostic Tests

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Myocarditis is an inflammation of the heart muscle. The symptoms vary widely, encompassing asymptomatic presentations to severe, acute manifestations.Clinical PresentationAsymptomatic cases: In some instances, myocarditis may be asymptomatic, with the infection resolving without intervention. These cases often go undetected unless discovered incidentally through diagnostic imaging or tests conducted for other reasons.General Early Symptoms: Early symptoms of myocarditis are non-specific and can...
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Myocarditis III: Medical Management01:14

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Myocarditis: Comprehensive Medical ManagementMyocarditis, the heart muscle inflammation, requires a comprehensive medical management strategy that addresses the underlying cause, provides supportive care, manages symptoms, and reduces cardiac workload.Infections and Autoimmune CausesAdminister appropriate antimicrobial therapy when an infectious agent causes myocarditis. For instance, penicillin treats infections caused by Group A Streptococcus. In cases where autoimmune processes are...
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Myocarditis I: Introduction01:21

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Myocarditis is inflammation of the myocardium, which is the muscular layer of the heart.EtiologyMyocarditis has a diverse etiology, including a wide range of infectious and non-infectious causes:Infectious CausesViral: Common viruses include Coxsackie A and B, adenovirus, parvovirus B19, enteroviruses, and influenza A.Bacterial: Examples include infections caused by Streptococcus, Staphylococcus, and Mycoplasma species.Rickettsial: Infections like Rocky Mountain spotted fever can result in...
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Myocarditis IV: Nursing Management01:22

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Myocarditis is an inflammatory condition of the myocardium requiring meticulous nursing management for optimal patient outcomes. Effective management begins with a thorough assessment of the patient's medical history, paying close attention to past infections, autoimmune disorders, travel history, and exposure to toxins or drugs. Recent viral infections and systemic diseases are particularly relevant due to their potential role in triggering myocarditis.Physical Examination and MonitoringThe...
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Myasthenia Gravis: Overview and Treatment01:20

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Myasthenia gravis is a neuromuscular transmission disorder characterized by weakness and increased fatigability of skeletal muscles. It is an autoimmune disease affecting approximately one in 2000 people, where antibodies against the α1 subunit of nicotinic acetylcholine receptors are produced.
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Myasthenia Gravis: Diagnostic Tests01:15

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Myasthenia gravis is an autoimmune condition affecting neuromuscular transmission, causing generalized weakness in skeletal muscles. Initial diagnoses rely on patients' signs, symptoms, and medical history. The challenge lies in distinguishing myasthenia from other muscular dystrophies. An important diagnostic feature is the significant improvement of symptoms after administering anticholinesterase inhibitors.
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Author Spotlight: Unveiling the Polyfunctionality and Heterogeneity in Immune Responses
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Polymyositis: The Comet Tail After COVID-19.

Said Amin1,2, Fawad Rahim1,2, Mohammad Noor1,2

  • 1Internal Medicine, Khyber Girls Medical College, Peshawar, PAK.

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|August 2, 2022
PubMed
Summary

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can trigger autoimmune disorders like polymyositis. This case highlights a patient’s recovery from COVID-19-related inflammatory myopathy with targeted treatment.

Keywords:
coronavirus disease 2019 (covid-19)muscle weaknesspolymyositisrheumatic disordersars-cov-2 (severe acute respiratory syndrome coronavirus-2)

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Area of Science:

  • Rheumatology
  • Infectious Diseases
  • Neurology

Background:

  • Infectious agents, including SARS-CoV-2, are increasingly implicated in autoimmune disorders.
  • SARS-CoV-2, initially viewed as a respiratory pathogen, is now associated with various autoimmune rheumatic conditions.
  • The pathogenesis of muscle injury in COVID-19 is often attributed to autoimmune inflammatory damage or cytokine storm.

Observation:

  • A 52-year-old female presented with significant muscle weakness (MRC grade 3/5), body aches, and fatigue four months post-mild COVID-19.
  • Clinical presentation included proximal muscle weakness and elevated muscle enzymes.
  • Diagnostic workup revealed an active myopathic process on electromyography and inflammatory myopathy on muscle biopsy.

Findings:

  • The patient was diagnosed with inflammatory polymyositis secondary to COVID-19.
  • Treatment with prednisolone and azathioprine led to a remarkable recovery of muscle strength to MRC grade 5/5 within four weeks.
  • This case adds to the limited reports of inflammatory polymyositis post-COVID-19, particularly in developing regions.

Implications:

  • This case underscores the potential for SARS-CoV-2 to induce delayed-onset autoimmune inflammatory myopathy.
  • Early diagnosis and immunosuppressive therapy can lead to significant functional recovery.
  • Further research is needed to elucidate the precise mechanisms linking SARS-CoV-2 to autoimmune myopathies.