AI Article Synopsis

Article Abstract

Adenomyomatous hyperplasia is most commonly found in the stomach, gallbladder, duodenum, and jejunum, while it is rarely found in the extrahepatic bile duct. A 62-year-old woman was referred to our institution with a diagnosis of common bile duct (CBD) stenosis which had been detected by endoscopic retrograde cholangiopancreatography (ERCP). Abdominal computed tomography with contrast medium revealed a thickening of the wall of the lower CBD, and this lesion was weakly enhanced by contrast medium in the arterial phase. ERCP revealed a 15-mm-long stenosis of the lower CBD, but no malignant cells were detected by either bile cytology or brush cytology. Because CBD cancer could not be ruled out, pylorus-preserving pancreatoduodenectomy was performed. Histopathologically, multiple hyperplastic glands without cellular atypia were present in the lower CBD wall. An immunohistochemical study showed fibroblasts with positive staining for alpha-smooth muscle actin surrounding the glands. The lesion was diagnosed to be adenomyomatous hyperplasia of the CBD. When a diagnosis of adenomyomatous hyperplasia of the CBD is difficult to make both preoperatively and intraoperatively, then a radical surgical procedure, such as a pancreatoduodenectomy, may be an effective treatment alternative.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00595-007-3558-9DOI Listing

Publication Analysis

Top Keywords

adenomyomatous hyperplasia
16
bile duct
12
lower cbd
12
common bile
8
contrast medium
8
hyperplasia cbd
8
cbd
7
adenomyomatous
4
hyperplasia common
4
bile
4

Similar Publications

Adenomyomatous hyperplasia and adenomyoma are rare benign inflammatory pseudotumors of the gallbladder arising from Rokitansky-Aschoff sinuses. Occurrence of these hyperplastic conditions in the Vaterian and biliary system is extremely rare and is a concern for gastroenterologists and surgeons in distinguishing them from primary malignancies of the biliary system. Definitive diagnosis by imaging or cytopathological examination is difficult; thus, surgical resection becomes the only choice in such cases to relieve the obstruction.

View Article and Find Full Text PDF

Background: The relationship between adenomyomatous hyperplasia of the Vaterian system(AV) and cancer is unclear, some reports suggest that AV is often combined with mucosal glandular dysplasia, but it is not clear whether mucosal glandular dysplasia is a risk factor for carcinogenesis of AV. The aim of this study was to retrospective analysis of role of ductal glandular dysplasia as a risk factor in the development of carcinoma in AV.

Methods: A total of 328 cases who underwent surgery with a final pathological diagnosis of adenomyomatous hyperplasia (AH) in the Chinese PLA General Hospital in BeiJing, China, between January 2005 and December 2021 were retrospectively collected.

View Article and Find Full Text PDF
Article Synopsis
  • * A cystoscopy revealed an obstructed bladder neck and a large mass, leading to a transurethral subtotal resection; post-surgery, PSA levels were low and no complications were noted.
  • * The histopathological findings confirmed massive adenomyomatous hyperplasia and the absence of disease recurrence during 17 months of follow-up, highlighting the need for further investigation into treatment options for similar cases.
View Article and Find Full Text PDF
Article Synopsis
  • A 70-year-old man was hospitalized due to jaundice and abdominal pain, with tests showing elevated liver enzymes and amylase levels.
  • Imaging studies revealed a thickened bile duct and stenosis, leading to the discovery of adenocarcinoma through a biopsy.
  • After a pancreatoduodenectomy, the pathology indicated carcinoma in situ linked to adenomyomatous hyperplasia, a condition not previously reported in relation to bile duct or ampulla carcinoma.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!