Skip to main content
Log in

An extremely rare case of symptomatic right hepatic duct diverticulum located outside the liver

  • Case Study
  • Published:
Pediatric Surgery International Aims and scope Submit manuscript

Abstract

Symptomatic hepatic duct diverticulum located outside the liver is extremely rare, with only one reported case. We encountered this anomaly and present our experience, focusing on surgical management. A 17-year-old-girl was referred to our institute because of recurrent right upper quadrant pain. At presentation, serum amylase, lipase, bilirubin, and transaminases were normal. White blood cell count and C-reactive protein were slightly raised. Ultrasonography and magnetic resonance cholangiopancreatography (MRCP) revealed a diverticulum-like lesion on the right side of the bile duct system appearing to overlap the gallbladder. The provisional diagnosis was type II choledochal cyst. Pancreaticobiliary malunion (PBMU) could not be confirmed on MRCP. The origin of the lesion could not be identified initially at laparotomy, but after repeated intraoperative cholangiography (IC) studies, the lesion was found to originate from a normal-sized right hepatic duct via a narrow duct. It was relatively easy to ligate the narrow duct and treat the lesion smoothly. IC also showed that the common bile duct was not dilated and that PBMU was absent. Histopathology showed the lesion to be a diverticulum of the bile duct epithelium. This is only the second report of a symptomatic hepatic duct diverticulum located outside the liver. Based on our experience, IC is particularly useful for the complete understanding of anomalous hepatobiliary duct anatomy and for planning surgical treatment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

References

  1. Schey WL, Pinsky SM, Lipschutz HS et al (1977) Hepatic duct diverticulum simulating a choledochal cyst. Am J Roentgenol 128:318–320

    CAS  Google Scholar 

  2. Todani T, Watanabe Y, Narusue M et al (1977) Congenital bile duct cysts: classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst. Am J Surg 134:263–269

    Article  PubMed  CAS  Google Scholar 

  3. Maxwell JW, Jackson FC, Davis WC et al (1967) Hepatodochal diverticulum. Am Surg 33:153–158

    PubMed  Google Scholar 

  4. Flowers MB, Ho KJ (1998) A rare common hepatic duct diverticulum causing fatal biliary obstruction and sepsis. Arch Pathol Lab Med 122:197–198

    PubMed  CAS  Google Scholar 

  5. Meyers C, Reynes CJ, Freeark RJ (1976) Diverticulum of the hepatic duct: a rare anomaly. Radiology 119:38

    PubMed  CAS  Google Scholar 

  6. Eisendrath DN (1920) Operative injury of the common and hepatic bile ducts. Surg Gynec Obstet 31:1–18

    Google Scholar 

  7. Ikematsu Y, Eto T, Matsumoto T et al (1994) Biliary diverticulum with pancreaticobiliary maljunction. Hepatogastroenterology 41:70–72

    PubMed  CAS  Google Scholar 

  8. Sato R, Fujii T, Chiba A, et al (2002) A case of Alonso-Lej’s type II, congenital cystic dilatation of the common bile duct (in Japanese). Gastroenterol Endosc 44:1191–1197

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Atsuyuki Yamataka.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kaneyama, K., Yamataka, A., Urao, M. et al. An extremely rare case of symptomatic right hepatic duct diverticulum located outside the liver. Ped Surgery Int 21, 1023–1026 (2005). https://doi.org/10.1007/s00383-005-1527-1

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00383-005-1527-1

Keywords

Navigation