Díaz Alcázar MDM, et al. Rev Esp Enferm Dig 2020.
ABSTRACT
We present the case of a 50-year-old male diagnosed with myasthenia gravis, secondary to thymoma or Lambert-Eaton syndrome during the study of repeated vomiting. Gastrointestinal symptoms persisted despite the treatment of the thymoma. He suffered from sigma volvulus that required sigmoidectomy 9 years after diagnosis. Neuromuscular junction disorders are not characterized by gastrointestinal involvement, as in our case. They have previously sporadically been related to intestinal motility dysfunction.
PMID:32496121 | DOI:10.17235/reed.2020.6846/2019
Source: https://pubmed.ncbi.nlm.nih.gov/3249612 ... 27&v=2.8.0
