Finsterer- Bancroft-Plenk手术与Bouveret综合征:罕见的关联。

IF 1.8
Philipe Franco do Amaral Tafner, Giulia Trucolo de Brito, Joao Guilherme Oliveira Vaz, Bruna Mattos Vanetti de Albuquerque, Ana Carolina Arantes, Ary Augusto de Castro Macedo, Valdir Tercioti Junior, João de Souza Coelho Neto, Nelson Adami Andreollo, Luiz Roberto Lopes
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引用次数: 0

摘要

消化性溃疡疾病(PUD)表现出不同的发展和严重程度。胃脘痛是患者最重要的主诉,并可能伴有其他并发症,如出血、穿孔和狭窄,并伴有合并症。Bouveret综合征是一种罕见的综合征,具有非特异性症状和长期的发展,其特征是由大胆结石通过胆囊-十二指肠瘘迁移而引起十二指肠梗阻。目前被称为Finsterer-Bancroft-Plenk技术,保留胃窦并去除胃窦黏膜,并伴有部分胃切除术。Finsterer-Bancroft-Plenk技术仍然是一种手术选择,面对继发于PUD的复杂十二指肠狭窄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Finsterer- Bancroft-Plenk operation and Bouveret's syndrome: a rare association.

Peptic ulcer disease (PUD) presents different spectrums of evolution and severity. Epigastric pain is the patient's most important complaint and may be associated with other complications, such as bleeding, perforations and stenosis, associated with comorbidities. Bouveret syndrome is a rare syndrome with nonspecific symptoms and prolonged evolution, characterizing duodenal obstruction by a large gallstone migrated through a cholecystoduodenal fistula. It is currently known as the Finsterer-Bancroft-Plenk technique, the preservation of the antrum and removal of the antral mucosa associated by partial gastrectomy. The Finsterer-Bancroft-Plenk technique is still a surgical option in the face of complex duodenal stenoses secondary to PUD.

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