¨A síndrome de Bouveret é uma forma rara de ileus biliar, em que a obstrução ocorre a nível duodenal. A raridade desta síndrome, associada a manifestações clínicas inespecíficas, contribui para que esta síndrome permaneça um importante desafio diagnóstico. Os sintomas clínicos não são específicos e é mais comumente apresentado com náuseas, vômitos, saciedade precoce e dor abdominal. A dor abdominal, as náuseas e os vómitos pós-prandiais de início súbito são os sintomas mais frequentes. Os achados radiológicos típicos compreendem a tríade de Rigler [presença de obstrução do intestino delgado e dilatação do estômago, pneumobilia (ar na árvore biliar) e cálculos ectópicos], que pode ser detectada em radiografias abdominais simples ou tomografia computadorizada abdominal, mas nem sempre está presente . A tomografia computadorizada também pode demonstrar a presença de fístula colecisteto-duodenal administrando material de contraste oral ou aéreo. A remoção do cálculos baixos impactados através da enterotomia ou gastrotomia ou litotripsia endoscópica é o tratamento usual. Em particular, as opções de tratamento não cirúrgico incluem litotripsia endoscópica mecânica, eletrohidráulica ou a laser e litotripsia de onda de choque extracorpórea, isoladas ou combinadas. No entanto, existe a possibilidade de migração distal de fragmentos, o que pode causar íleo distal e eventualmente requer remoção cirúrgica¨

 

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Successful endoscopic treatment of Bouveret syndrome in a patient with choledochoduodenal fistula complicating duodenal ulcer

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Bouveret´s syndrome: revising gallstone obstruction of he duodenum

Dilip Dan, Don W. Collure, Eddie L. Hoover

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■ by Dr Paulo Fernando Leite

Cardiologia – Centro Médico Unimed BH

Rua Gonçalves Dias 202

Belo Horizonte/MG/Brasil

31 30033306       /   40204020

CRMMG: 7026

Email: pfleite1873@gmail.com