(G13.0*) Paraneoplastic neuromyopathy and neuropathy

More details coming soon

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NaN% mortality rate associated with the disease paraneoplastic neuromyopathy and neuropathy

Diagnosis paraneoplastic neuromyopathy and neuropathy is diagnosed Prevalent in Women Only

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Men receive the diagnosis paraneoplastic neuromyopathy and neuropathy

0 (No mortality)

Died from this diagnosis.

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Women receive the diagnosis paraneoplastic neuromyopathy and neuropathy

0 (No mortality)

Died from this diagnosis.

Risk Group for the Disease paraneoplastic neuromyopathy and neuropathy - Men and Women aged 0

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No Cases of the Disease Paraneoplastic neuromyopathy and neuropathy identified in Men
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Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 0-95+
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No Cases of the Disease Paraneoplastic neuromyopathy and neuropathy identified in Men

Disease Features paraneoplastic neuromyopathy and neuropathy

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Absence or low individual and public risk
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Paraneoplastic neuromyopathy and neuropathy - what does this mean

Paraneoplastic neuromyopathy and neuropathy is a rare disorder which is caused by an underlying malignant tumor. it is characterized by the presence of an antibody which attacks the peripheral nervous system and causes damage to the nerve cells, leading to muscle weakness, fatigue, and sensory disturbances.

What happens during the disease - paraneoplastic neuromyopathy and neuropathy

Paraneoplastic neuromyopathy and neuropathy is a rare condition caused by an immune response to a cancerous tumor. the immune system mistakenly attacks the healthy nerves of the body, leading to damage of the peripheral nerves. this damage causes muscle weakness, pain, tingling, and numbness in the affected areas. the underlying cause of the condition is not fully understood, but it is believed that the tumor releases certain proteins that trigger an autoimmune response in the body.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Review of patient history and physical examination
  • Blood tests to assess for autoantibodies
  • Electromyography (EMG) and nerve conduction studies
  • Imaging studies such as CT scan or MRI
  • Biopsy of the affected nerve or muscle
  • Neuropsychological testing
  • Genetic testing

Treatment and Medical Assistance

Main Goal: Treat the symptoms and improve the quality of life of the patient.
  • Prescribe medications to reduce inflammation and pain.
  • Provide physical therapy to improve muscle strength and coordination.
  • Recommend lifestyle changes such as regular exercise and a healthy diet.
  • Refer to a neurologist for further evaluation and treatment.
  • Refer to a physical therapist for assistance with mobility.
  • Refer to an occupational therapist for assistance with activities of daily living.
  • Refer to a speech-language pathologist for assistance with speech and swallowing.
  • Refer to a nutritionist for assistance with dietary modifications.
  • Refer to a mental health professional for counseling and support.
  • Provide patient education and support.
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No Hospitalization Required
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Average Time for Outpatient Care Not Established

Paraneoplastic neuromyopathy and neuropathy - Prevention

Paraneoplastic neuromyopathy and neuropathy can be prevented by avoiding risk factors for cancer, such as smoking, and by getting timely screenings and regular checkups. eating a healthy diet, exercising regularly, and avoiding excessive alcohol consumption can also help reduce the risk of developing this condition.