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Oddi 括约肌功能障碍。

Sphincter of Oddi dysfunction.

机构信息

Service de gastroentérologie, Hôpital Nord, Chemin des Bourrelys, 13915 Marseille cedex 20, France.

Service de gastroentérologie, Hôpital Nord, Chemin des Bourrelys, 13915 Marseille cedex 20, France.

出版信息

J Visc Surg. 2022 Mar;159(1S):S16-S21. doi: 10.1016/j.jviscsurg.2022.01.008. Epub 2022 Feb 4.

Abstract

Sphincter of Oddi dysfunction (SOD) is a benign non-tumoral disorder of the major papilla. It occurs mainly after cholecystectomy but can also occur before surgery. Biliary pain and biliary colic are the most frequent symptoms although recurrent pancreatic pain or pancreatitis can also be presenting symptoms. In about half of the cases, there is a fibrotic stricture of the sphincter of Oddi, probably secondary to the passage of biliary stones, while in the remaining half, the syndrome is due to ampullary motility disorders. The diagnosis of SOD first requires exclusion of choledocholithiasis or ampullary tumor, by means of ERCP, endoscopic ultrasound or magnetic resonance imaging. Findings on biliary manometry will establish the diagnosis, but this technique is performed less and less often because its high risk of inducing pancreatitis discourages its use as a diagnostic procedure. Biliary scintigraphy offers a risk-free alternative albeit with lower sensitivity. Medical treatment relies on the administration of trimebutine and nitroglycerine when pain occurs. Their efficacy is moderate. Sometimes patients are referred for endoscopic sphincterotomy. Endoscopic treatment should be performed only for patients with biliary pain associated with hepatic function disorders and/or bile duct dilatation. Practicians and patients should be aware that endoscopic sphincterotomy in this clinical setting is associated with a high risk of pancreatitis and its efficacy is limited in patients with pain but without laboratory anomalies or dilatation of the biliary duct (type III Milwaukee classification). Patients with Milwaukee classification type III disorders have mostly functional complaints or psychosocial disabilities and require only medical management.

摘要

Oddi 括约肌功能障碍(SOD)是一种主要乳头的良性非肿瘤性疾病。它主要发生在胆囊切除术后,但也可发生在手术前。胆绞痛和胆绞痛是最常见的症状,尽管复发性胰痛或胰腺炎也可能是首发症状。在大约一半的病例中,Oddi 括约肌存在纤维性狭窄,可能继发于胆管结石的通过,而在另一半病例中,该综合征是由于壶腹运动障碍引起的。SOD 的诊断首先需要通过 ERCP、内镜超声或磁共振成像排除胆总管结石或壶腹肿瘤。胆道测压可确立诊断,但由于其诱发胰腺炎的高风险,该技术的应用越来越少,因为它不适合作为诊断程序。胆道闪烁显像提供了一种无风险的替代方法,尽管其敏感性较低。当疼痛发生时,药物治疗依赖于曲美布汀和硝酸甘油的应用。它们的疗效是中等的。有时患者会接受内镜下括约肌切开术。只有当肝功能障碍和/或胆管扩张与胆绞痛相关时,才应进行内镜治疗。临床医生和患者应意识到,在这种临床情况下,内镜下括约肌切开术与胰腺炎的高风险相关,并且对于仅有疼痛但无实验室异常或胆管扩张(Milwaukee 分类 III 型)的患者,其疗效有限。Milwaukee 分类 III 型疾病的患者大多有功能性投诉或社会心理障碍,仅需药物治疗。

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