2022, Number 1
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Rev Neurol Neurocir Psiquiat 2022; 50 (1)
About a case of miastenia gravis seen at our hospital
Molina-León Á, Tudor-Franco C
Language: Spanish
References: 15
Page: 26-32
PDF size: 154.33 Kb.
ABSTRACT
The postsynaptic disorder that represents myasthenia gravis is an autoimmune attack of anti-acetylcholine Ach-receptor antibodies that produces a typical triad: ptosis, diplopia and fatigability, and severely affects the facial and proximal muscles, resulting, among other abnormalities, in weakness of speech, chewing and swallowing, and may even affect the respiratory muscles. We present a case of a 58-year-old male patient, with previous consultations in the emergency department for a month due to severe choking problems, both with solids and liquids. His medical history includes allergy to penicillin, ibuprofen and tramadol, extrinsic bronchial asthma, childhood poliomyelitis and unintervened fracture of the greater trochanter. The patient underwent exhaustive analysis and repetitive distal stimulation and Jitter with proximal axonal microstimulation. The results corroborate the diagnoses used in relation to this muscular etiopathogenesis.
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