Arellano-Aguilar Gregorio, Núñez-Mojica Erik Santiago, Gutiérrez-Velazco José Luis, Domínguez-Carrillo Luis Gerardo
División de Medicina, Universidad de Guanajuato. León, Gto., México.
Interno de pregrado. Hospital Ángeles León, Universidad de Guanajuato. León, Gto., México.
Cir Cir. 2018;86(1):79-83. doi: 10.24875/CIRU.M18000006.
Neurological paraneoplastic syndromes are rare, occur in 0.01% of all cancer patients; like part of them, the Lambert-Eaton syndrome is an autoimmune presynaptic disorder of neuromuscular transmission characterized by muscle weakness and neurovegetative dysfunction, and often associated with small cell lung cancer.
A 72 years old female with a family history of lung cancer and leukemia, with 7 months of dry cough and 3 months with waist and pelvic muscle weakness, oropharyngeal dysphagia, dry mouth, chronic constipation and weight loss of 10 kg. Physical examination: patient prostrated; clinical muscle examination: pelvic muscles waist -3/5 and -4/5 the rest; diminished reflexes. Laboratory normal parathormone and hypercalcemia. With electrophysiological study and positive anti-voltage-gated calcium channel antibodies, confirming Lambert-Eaton syndrome and imaging studies with neoplastic condition in brain, liver and kidney, with unspecified primary origin.
