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A Case of Congenital Esophageal Stenosis Due to Tracheobronchial Remnants in Adult / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy ; : 21-25, 2003.
Artigo em Coreano | WPRIM | ID: wpr-149931
ABSTRACT
Congenital stenosis of the esophagus is a rare form of esophageal stenosis in adults. The main causes of congenital esophageal stenosis are the esophageal web, esophageal stricture due to tracheobronchial remnants, and idiopathic esophageal muscular hypertrophy. Recently we have experienced a 32-year-old male with dysphagia, indigestion, postprandial chest discomfort who was diagnosed as congenital esophageal stenosis due to tracheobronchial remnant. The esophagogram showed stricture of the distal esophagus with secondary proximal dilatation and endoscopic finding revealed marked stenosis on the distal esophagus with normal surrounding mucosa. The esophageal manometric finding showed decreased body peristalsis and incomplete relaxation of the lower esophageal sphincter. The patient was treated by surgical resection of the stenotic segment with end to end anastomosis. We report this rare case of adult type tracheobronchial remnant with analysis of various worldwide report and with brief review of literature.
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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Peristaltismo / Relaxamento / Tórax / Transtornos de Deglutição / Constrição Patológica / Esfíncter Esofágico Inferior / Dilatação / Dispepsia / Estenose Esofágica / Esôfago Limite: Adulto / Humanos / Masculino Idioma: Coreano Revista: Korean Journal of Gastrointestinal Endoscopy Ano de publicação: 2003 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Peristaltismo / Relaxamento / Tórax / Transtornos de Deglutição / Constrição Patológica / Esfíncter Esofágico Inferior / Dilatação / Dispepsia / Estenose Esofágica / Esôfago Limite: Adulto / Humanos / Masculino Idioma: Coreano Revista: Korean Journal of Gastrointestinal Endoscopy Ano de publicação: 2003 Tipo de documento: Artigo