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伴有正常及相对较长共同通道的胰胆反流导致儿童胆结石和急性胰腺炎

Pancreaticobiliary Reflux with Normal and Relatively Long Common Channels Causing Cholelithiasis and Acute Pancreatitis in Children.

作者信息

Kouchi Katsunori, Takenouchi Ayako, Matsuoka Aki, Yoshizawa Hiroko, Nakata Chikako

机构信息

Department of Pediatric Surgery, Tokyo Women's Medical University, Tokyo 162-8666, Japan.

Department of Pediatric Surgery, Chiba University, Chiba 263-8522, Japan.

出版信息

J Clin Med. 2024 Dec 16;13(24):7650. doi: 10.3390/jcm13247650.

Abstract

Pancreaticobiliary maljunction (PBMJ) has a long common channel (CC) that causes pancreaticobiliary reflux (PBR), which has been implicated in gallstones, cholangiocarcinoma, and pancreatitis. By contrast, PBR has occurred in cases with normal and longer CCs than normal but shorter than PBMJ. This pathophysiology has been primarily reported in adults and rarely in children. We sometimes observe this pathophysiology in children with pancreatitis and cholelithiasis. Herein, we report the clinical figures on the diagnosis of children with PBR in normal and relatively long CCs. This study included seven children who complained of refractory pancreatitis and cholelithiasis diagnosed with PBR in normal and relatively long CCs at our institution from August 2018 to September 2024. We measured the lengths of their CCs and sphincter of Oddi muscles via endoscopic retrograde cholangiopancreatography (ERCP) and cholangiography. In addition, amylase and lipase levels in bile juice were measured. All seven children demonstrated elevated amylase and lipase levels in bile juice obtained from gallbladder drainage and/or the common bile duct. ERCP and cholangiography indicated 2.2-5.5-mm lengths of CCs in their cases, which are normal lengths in two cases and relatively longer (0.3-1.1 mm: mean 0.6 mm) than the normal upper limit of CC in children in five cases, with their CCs shorter than the sphincters of Oddi. All children underwent extrahepatic bile duct resection and bilio-jejunal anastomosis, demonstrating no clinical symptom recurrence postoperatively. Some children with cholelithiasis and pancreatitis exhibit normal and relatively long CCs, causing PBR and inducing gastrointestinal diseases. Careful investigation by ERCP and cholangiography focused on the CC length, and pancreatic enzyme level assessments in bile juice are useful for diagnosing PBR in children with cholelithiasis and refractory pancreatitis.

摘要

胰胆管合流异常(PBMJ)具有一个长的共同通道(CC),可导致胰胆管反流(PBR),这与胆结石、胆管癌和胰腺炎有关。相比之下,在CC正常且比正常长但比PBMJ短的情况下也会发生PBR。这种病理生理学主要在成人中报道,在儿童中很少见。我们有时在患有胰腺炎和胆石症的儿童中观察到这种病理生理学。在此,我们报告了在正常和相对较长的CC中诊断儿童PBR的临床数据。本研究纳入了7名儿童,他们在2018年8月至2024年9月期间在我们机构被诊断为患有PBR的难治性胰腺炎和胆石症,其CC正常且相对较长。我们通过内镜逆行胰胆管造影(ERCP)和胆管造影测量了他们的CC长度和Oddi括约肌长度。此外,还测量了胆汁中的淀粉酶和脂肪酶水平。所有7名儿童从胆囊引流和/或胆总管获取的胆汁中淀粉酶和脂肪酶水平均升高。ERCP和胆管造影显示,他们病例中的CC长度为2.2 - 5.5毫米,其中2例为正常长度,5例比儿童CC正常上限相对更长(0.3 - 1.1毫米,平均0.6毫米),且他们的CC比Oddi括约肌短。所有儿童均接受了肝外胆管切除和胆肠吻合术,术后均未出现临床症状复发。一些患有胆石症和胰腺炎的儿童表现出正常且相对较长的CC,导致PBR并引发胃肠道疾病。通过ERCP和胆管造影仔细检查CC长度,并评估胆汁中的胰酶水平,对于诊断患有胆石症和难治性胰腺炎的儿童的PBR很有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d1/11677763/164ff1482d8a/jcm-13-07650-g001.jpg

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