| Literature DB >> 26504881 |
Bashar Mohamad1, Amit Bhatt2, Arthi Kumaravel2, Federico Aucejo3, Sunguk Jang2, Tyler Stevens2, John Vargo2, Mansour Parsi2.
Abstract
We present a 42-year-old man with a 1-month history of painless jaundice, dark urine, clay-colored stools, and a 13.5-kg weight loss. Laboratory tests revealed elevated liver enzymes and CA19-9. Imaging showed dilation of both the intra- and extrahepatic bile ducts, narrowing of the bile duct at the junction of the common bile duct and common hepatic duct, and a hypoechoic mass involving the neck of the gallbladder and the muscularis propria of the duodenum. Examination of the resected gallbladder and perihilar nodes ruled out malignancy and revealed a diffuse inflammatory infiltrate of giant histiocytes with clear, lipid-containing cytoplasm (xanthoma cells), consistent with xanthogranulomatous cholecystitis.Entities:
Year: 2015 PMID: 26504881 PMCID: PMC4612761 DOI: 10.14309/crj.2015.100
Source DB: PubMed Journal: ACG Case Rep J ISSN: 2326-3253
Figure 1ERCP of bile duct narrowing at the junction of the common bile and common hepatic ducts, with dilation of the biliary tree proximal to the narrowing.
Figure 2EUS view of hypoechoic mass involving (A) the neck of the gallbladder and (B) the muscularis propria layer of the duodenum.
Figure 3Pathologic examination of resected gallbladder showing a diffuse inflammatory infiltrate of giant histiocytes with clear, lipid-containing cytoplasm (xanthoma cells).