Myoglobinuria Paralytic

Myoglyconulites, or (myopathies of central origin), are a pathological condition caused by traumatic muscle dystrophy due to circulatory disorders in the brain stem. The disease is characterized by progressive pain in the neck and chest, difficulty moving and gait, and dysfunction of the pelvic organs. The most common form is idiopathic. Treatment is based on the administration of analgesics, proserine and replacement therapy.

The first stage is vascular-segmental, the next begins from damage to the cranial nerves in the trunk, muscles due to the fact that the function of muscle innervation is disrupted. In the third stage, muscle paralysis and loss of control over limb functions appear. Speech is disrupted, chanting-type speech develops, breathing becomes shallow and rapid, blood pressure changes, blood circulation in the skeletal tissues worsens, atrophy of muscle tissue and skin atrophy are provoked. Subsequently, myocardial damage and pneumonia develop. The disease often has an atypical course; there are only symptomatic forms. The duration of the phase is months, less often – years. Death occurs from pneumonia, heart failure and circulatory and circulatory disorders. Rarely, polyneuropathy may occur.

Myoglobinemia - or myoparalytic acute abdomen syndrome - is considered a rare disease. It is characterized by narrowing and disruption of the functioning of the genitourinary organs in humans. Severe illness can lead to death. In the 2016 International Classification of Diseases, it was assigned the code R82.0. Examinations are carried out by urologists and nephrologists.