Megaesófago como complicación de acalasia: Reporte de caso y revisión narrativa de la literatura

Julián Rondón-Carvajal, Carolina Ardila-Hani, Albis Hani-Ardila, Rómulo Vargas-Rubio, Ana María Leguízamo-Naranjo, Raúl Cañadas-Garrido, Gerardo Puentes-Leal

Producción: Contribución a una revistaArtículorevisión exhaustiva

1 Cita (Scopus)

Resumen

Megaesophagus occurs in between 5% and 20% of patients with achalasia. It is a primary esophageal motor disorder that has been known for more than 300 years. It should be considered in all patients with dysphagia that is not explained by an obstructive or inflammatory process after a detailed endoscopic study. The following is the case of a patient with progressive dysphagia, in whom megaesophagus was documented as a complication of untreated, long-standing achalasia. Chagas disease was ruled out by enzyme immunoassay (ELISA) and indirect immunofluorescence (IF), as recommended by current guidelines. Given the low frequency of this entity in our environment and the therapeutic implications for patients with achalasia, a narrative literature review was carried out to describe its diagnosis and treatment alternatives.

Título traducido de la contribuciónMegaesophagus as a complication of achalasia: Case report and narrative literature review
Idioma originalEspañol
Páginas (desde-hasta)551-557
Número de páginas7
PublicaciónRevista Colombiana de Gastroenterologia
Volumen35
N.º4
DOI
EstadoPublicada - 01 oct. 2020
Publicado de forma externa

Palabras clave

  • Achalasia
  • Dysphagia
  • Esophageal motility
  • High-resolution manometry
  • Megaesophagus

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