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反流相关性胆囊病:对76例胰管与胆总管超Oddi联合(胰胆合流异常)患者的胆囊进行分析,阐明了作为癌前病变的黏膜增生的特定诊断模式。

Reflux-Associated Cholecystopathy: Analysis of 76 Gallbladders From Patients With Supra-Oddi Union of the Pancreatic Duct and Common Bile Duct (Pancreatobiliary Maljunction) Elucidates a Specific Diagnostic Pattern of Mucosal Hyperplasia as a Prelude to Carcinoma.

作者信息

Muraki Takashi, Memis Bahar, Reid Michelle D, Uehara Takeshi, Ito Tetsuya, Hasebe Osamu, Okaniwa Shinji, Horigome Naoto, Hisa Takeshi, Mittal Pardeep, Freedman Alexa, Maithel Shishir, Sarmiento Juan M, Krasinskas Alyssa, Koshiol Jill, Adsay Volkan

机构信息

Departments of *Pathology and Laboratory Medicine **Radiology ‡‡Surgery, Emory University School of Medicine ††Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA Departments of †Gastroenterology ‡Pathology, Shinshu University Hospital §Department of Gastroenterology, Nagano Municipal Hospital Departments of ∥Gastroenterology ¶Department of Surgery, Iida Municipal Hospital #Department of Gastroenterology, Saku Center Hospital, Nagano, Japan §§Division of Cancer Epidemiology and Genetics, National Institute of Health, Bethesda, MD.

出版信息

Am J Surg Pathol. 2017 Sep;41(9):1167-1177. doi: 10.1097/PAS.0000000000000882.

Abstract

Pancreaticobiliary maljunction (PBM) is the anomalous union of the main pancreatic duct and common bile duct outside the Oddi-sphincter, allowing the reflux of pancreatic juice to the gallbladder. There is only limited awareness and understanding of the pathologic correlates of this condition, mostly from Japan; this entity is largely unrecognized in the West. In this study, 76 gallbladders from patients with PBM (64 from Japan; 12 from the United States) were analyzed and contrasted with 66 from non-PBM patients. These were predominantly females (54 vs. 22), mean age, 53 (range: 14 to 81). Cholelithiasis was uncommon (16% vs. 80% in non-PBM, P<0.01) whereas cholesterolosis was more common (49% vs. 29%, P=0.02) suggesting an altered chemical milieu. There was a distinctive diffuse mucosal hyperplasia (82% vs. 42%, P<0.01) with markedly elongated folds (mean: 1.1 vs. 0.7 mm, P<0.01) composed of compact villoglandular proliferation, often showing broad-based pushing into muscle, accompanied by prominent and more complex Rokitansky-Aschoff sinus formation (2.0 vs. 1.0/cm, P<0.01) at the base. At the tips, this villiform hyperplasia displayed frequent horizontal bridging of the folds (68% vs. 47%, P=0.01), bulbous dilatation (52% vs. 21%, P<0.01) as well as deposition of a peculiar amyloid-like hyaline material (56% vs. 15%, P<0.01). Despite paucity of inflammation and gallstones, findings attributed to mucosal injury were common including: pyloric gland metaplasia (70% vs. 48%, P=0.01) and intestinal metaplasia (24% vs. 6%, P<0.01). Invasive gallbladder carcinoma was present in 22 (29%) of the cases with 6 of these (27%) arising in association with intracholecystic papillary tubular neoplasm. Five cases had bile duct carcinoma at the time of cholecystectomy and 1 developed it 4 years after. In conclusion, gallbladders with patients with PBM display a distinctive pattern of mucosal hyperplasia with distinguishing features, which in constellation render it a microscopically diagnosable specific entity. We propose to refer to this entity as "reflux-associated cholecystopathy." Recognition of the pathologic characteristics of this entity is important so that investigation for, as well as treatment and prevention of, PBM-associated complications (biliary tract cancers and pancreatitis) can be instituted. This group also offers a distinct model of carcinogenesis (chemical rather than inflammatory) in the gallbladder for cancer researchers to scrutinize.

摘要

胰胆管合流异常(PBM)是指主胰管与胆总管在Oddi括约肌外异常汇合,使得胰液反流至胆囊。目前对于这种疾病病理相关性的认识和理解非常有限,大多来自日本;在西方,这一实体在很大程度上未被认识。在本研究中,对76例PBM患者的胆囊(64例来自日本,12例来自美国)进行了分析,并与66例非PBM患者的胆囊进行对比。这些患者以女性为主(54例对22例),平均年龄53岁(范围:14至81岁)。胆石症并不常见(16%对非PBM患者中的80%,P<0.01),而胆固醇沉着症更为常见(49%对29%,P=0.02),提示化学环境发生改变。存在一种独特的弥漫性黏膜增生(82%对42%,P<0.01),褶皱明显延长(平均:1.1对0.7mm,P<0.01),由紧密的绒毛腺增生组成,常呈宽基底向肌层内推挤,同时在基底处伴有显著且更复杂的罗-阿窦形成(2.0对1.0/cm,P<0.01)。在顶端,这种绒毛状增生表现为褶皱频繁水平桥接(68%对47%,P=0.01)、球样扩张(52%对21%,P< /0.01)以及一种特殊的淀粉样透明物质沉积(56%对15%,P<0.01)。尽管炎症和胆结石较少,但归因于黏膜损伤的发现很常见,包括:幽门腺化生(70%对48%,P=0.01)和肠化生(24%对6%,P<0.01)。22例(29%)病例存在浸润性胆囊癌,其中6例(27%)与胆囊内乳头状管状肿瘤相关。5例在胆囊切除时患有胆管癌,1例在4年后发生胆管癌。总之,PBM患者的胆囊呈现出一种具有独特特征的黏膜增生模式,这些特征共同使其在显微镜下成为可诊断的特定实体。我们建议将这一实体称为“反流相关性胆囊病”。认识这一实体的病理特征很重要,以便能够开展对PBM相关并发症(胆道癌和胰腺炎)的调查、治疗和预防。这一组病例也为癌症研究人员提供了一种独特的胆囊致癌模型(化学性而非炎症性)以供研究。

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