Case Reports in Transplantation

Case Reports in Transplantation / 2013 / Article

Case Report | Open Access

Volume 2013 |Article ID 314292 |

Yinka K. Davies, Cynthia J. Tsay, Dario V. Caccamo, Kathleen M. Cox, Ricardo O. Castillo, Kenneth L. Cox, "Successful Treatment of Recurrent Primary Sclerosing Cholangitis after Orthotopic Liver Transplantation with Oral Vancomycin", Case Reports in Transplantation, vol. 2013, Article ID 314292, 5 pages, 2013.

Successful Treatment of Recurrent Primary Sclerosing Cholangitis after Orthotopic Liver Transplantation with Oral Vancomycin

Academic Editor: J. Kaneko
Received24 Dec 2012
Accepted22 Jan 2013
Published24 Feb 2013


Primary sclerosing cholangitis (PSC) is a progressive, cholestatic disease of the liver that is marked by inflammation of the bile ducts and damage to the hepatic biliary tree. Approximately 60–70% of patients also have inflammatory bowel disease and progression of PSC can lead to ulcerative colitis and cirrhosis of the liver. Due to limited understanding of the etiology and mechanism of PSC, the only existing treatment option is orthotopic liver transplantation (OLT); however, recurrence of PSC, after OLT is estimated to be between 5% and 35%. We discuss the successful treatment of a pediatric patient, with recurrent PSC, after OLT with oral Vancomycin.

1. Introduction

Primary sclerosing cholangitis (PSC) is a progressive inflammatory disease, of unknown etiology and with significant morbidity and mortality, which damages the intra- and/or extrahepatic biliary tree leading to portal hypertension and cirrhosis of the liver. The clinical course is variable including hepatobiliary carcinoma, especially cholangiocarcinoma in 6–20% of patients [16]. Additionally, it is estimated that 60–70% of people with PSC have inflammatory bowel disease [7, 8]. Orthotopic liver transplantation (OLT) is the only treatment option for patients with end-stage liver disease due to the progressive damage caused from PSC [9, 10]. The recurrence of PSC in the new graft is estimated to be between 5–35% [1113]. We report the successful treatment of a patient after OLT, who had shown recurrence of disease, with oral Vancomycin.

2. Case Report

A 12-year-old girl presented with a three-week history of jaundice and lethargy, with periumbilical pain every other day. There had been no recent travel or sick contacts. Screening tests revealed platelet level was low (89 K/uL; normal range 150 to 400). Antinuclear Antibody (ANCA) was positive with a homogeneous pattern, and Antinuclear Antibody Titer was elevated (640; normal range <40). Serum copper was normal at 1065 ug/L and ceruloplasmin was normal at 24 mg/dL. γ-Glutamyl transpeptidase (GGT) level was elevated (139 U/L; reference range from 5 to 36). C-Reactive Protein (CRP) was elevated at 2.80 mg/dL; reference range was from 0.0 to 0.5. PTT was elevated at 48.6 sec; normal range was from 23.3 to 33.8. Prothrombin Time was elevated at 21.0 sec; normal range was from 11.8 to 14.2. INR was increased to 1.9 sec; normal range was from 0.9 to 1.1. Erythrocyte sedimentation rate (ESR) was elevated at 107 mm/hr; bilirubin was elevated at 3.5 mg/dL, and ammonia was elevated at 55 umol/L. Patient underwent an open liver biopsy, which demonstrated the hepatic parenchyma being completely replaced by extensive compartmentalizing fibrosis and regenerative nodules. There was marked bile duct proliferation in the fibrotic areas. The fibrous septae showed a dense inflammatory infiltrate that consisted predominantly of small lymphocytes admixed with plasma cells and neutrophils. There was prominent interface hepatitis at the periphery of the inflamed septae. There was also a component of acute cholangitis showing focal bile duct infiltration and destruction by inflammatory cells, but most of the bile ducts were intact. There was minimal intrahepatocytic cholestasis, but no significant cholestasis was present in the large bile ducts (Figures 1(a) and 1(b)). She underwent colonoscopy and colonic biopsies which demonstrated focal cryptitis, occasional crypt abscesses, and some crypt distortion, mainly in the descending and sigmoid colon, correlating with her serologic marker ANCA, elevated at 640 (Figures 1(g) and 1(h)) consistent with ulcerative colitis. The patient was diagnosed with primary sclerosing cholangitis with inflammatory bowel disease (ulcerative colitis).

She underwent an orthotopic liver transplant three months later with postoperative complications consisting of hypertension. She was discharged home on postoperative day ten. Her postoperative medications included Prograf (Tacrolimus), CellCept (Mycophenolate), Prednisone, Actigall (Ursodiol), Magnesium, Septra (Trimethoprim and Sulfamethoxazole), and Valcyte (Valganciclovir). Over the next three years she did well weaning off everything except Prograf and CellCept. On routine labs (three years after transplant) she was found to have an elevated alkaline phosphatase level (204 U/L; normal range from 50 to 136). Her aspartate aminotransferase (AST) was elevated (267 U/L; normal range from 15 to 37). Her alanine aminotransferase (ALT) was elevated (290 U/L; normal range from 30 to 65). Her GGT was also elevated (309 U/L; normal range from 5 to 55). Her sedimentation rate was elevated (25 mm/hr; normal range from 0 to 20). EBV and CMV titers were negative and she had a therapeutic Prograf level of 7.9.

The patient underwent liver biopsy to distinguish between liver rejection or recurrence of primary sclerosing cholangitis. The transplanted liver biopsy demonstrated prominent portal inflammation consisting of large numbers of plasma cells and lymphocytes and rare neutrophils and eosinophils. There was prominent interface inflammation with occasional acidophil bodies near the limiting plate. There was mild to moderate bile ductular proliferation with very prominent lymphocytic infiltration of the bile ducts. Some of the bile ductules showed branching and there was concentric inflammation and “onion skin” fibrosis around bile ductules. Overall, the lobular parenchyma was unremarkable. There was lymphocytic endothelialitis. Trichrome stain demonstrated little periportal fibrosis and no evidence of bridging fibrosis. Iron stain was unremarkable. The biopsy was compatible with recurrent primary sclerosing cholangitis (Figures 1(c) and 1(d)). The lack of eosinophils in the portal infiltrate was more consistent with recurrent disease rather than acute rejection.

She was treated for recurrent primary sclerosing cholangitis. Her immunosuppressant medication remained the same and oral Vancomycin was added to the regimen. She received 500 mg orally three times a day of Vancomycin. During the course of her treatment with oral Vancomycin, liver enzymes (AST, ALT, GGT, ESR, and CRP) returned to normal values (Figure 2). The patient is currently on Vancomycin and remains well, to date, with normal laboratory values. Her repeat liver biopsy after three years from the recurrence of her primary sclerosing cholangitis showed no evidence of onion skin around the large bile duct and no inflammation of the bile ducts (Figures 1(e) and 1(f)). Comparison of biopsy photos before and after Vancomycin reveals a return to normal liver structure and anatomy (Figure 3).

3. Discussion

In this paper, we describe the successful use of oral Vancomycin in the treatment of recurrent PSC, after OLT. Currently, there is no universally accepted treatment for PSC; progressive cirrhosis of the liver inevitably leads to the need for liver transplantation in most patients. The majority of available therapeutic options, such as immunosuppressants, corticoid steroids, and ursodeoxycholic acid (UDCA), deal with complications resulting from PSC and do not inhibit progressive damage from the disease itself [14]. Studies have demonstrated that while UDCA can lead to improvements in biochemical markers, the potential for PSC recurrence requiring OLT is relatively high [15, 16]. Therefore, liver transplantation is the only life-extending option for individuals with advanced stage liver disease. Most data regarding PSC deals with adult cases, and some evidence has shown that the course of the disease in adolescents may follow a unique clinical course, notably an elevation in autoimmune features such as elevated antinuclear antibodies [17]. While juvenile PSC is rare, it contributes to around 2% of pediatric LT annually. The limited number of effective treatment options is primarily due to the unknown pathogenesis of PSC, although some speculate that the primary disease agent is from an enteric bacterial infection.

Previous studies have demonstrated that oral Vancomycin is a viable treatment for early stage PSC, before extensive cirrhosis of the liver is present [18, 19]. An extended clinical study demonstrated that long-term treatment with oral Vancomycin in fourteen juvenile PSC with IBD cases led to the normalization of liver blood markers and reversal of histological abnormalities. However, relapse in GGT and ALT occurred after treatment was suspended [19]. Oral Vancomycin is an immunomodulating bacteria glycopeptide antibiotic that is used to treat gram-positive infections with staphylococcal and has been shown to be poorly absorbed systemically [20, 21]. Vancomycin could also be acting as an anti-inflammatory agent, suggesting that PSC could be an autoimmune disease.

The successful use of oral Vancomycin in reversing the effects of early stage PSC can help develop current understanding regarding the mechanism of the disease. Ongoing clinical trials can potentially lead to new information in regard to the etiology and pathology of the disease. Specifically, this case demonstrates that oral Vancomycin was effective in a case of recurrent PSC after OLT, suggesting that the disease mechanism is not confined within the liver and has external causes—potentially from the backflow of gut bacteria or the spread of gut bacteria through the blood. However, larger cohorts of children with PSC are needed for a more thorough, longitudinal investigation regarding the mechanism, pathogenesis, and treatment of juvenile PSC.


  1. A. Wee, J. Ludwig, and R. J. Coffey, “Hepatobiliary carcinoma associated with primary sclerosing cholangitis and chronic ulcerative colitis,” Human Pathology, vol. 16, no. 7, pp. 719–726, 1985. View at: Google Scholar
  2. C. B. Rosen, D. M. Nagorney, R. H. Wiesner, R. J. Coffey, and N. F. LaRusso, “Cholangiocarcinoma complicating primary sclerosing cholangitis,” Annals of Surgery, vol. 213, no. 1, pp. 21–25, 2001. View at: Google Scholar
  3. J. M. Farrant, K. M. Hayllar, M. L. Wilkinson et al., “Natural history and prognostic variables in primary sclerosing cholangitis,” Gastroenterology, vol. 100, no. 6, pp. 1710–1717, 1991. View at: Google Scholar
  4. U. Broomé, R. Olsson, L. Lööf et al., “Natural history and prognostic factors in 305 Swedish patients with primary sclerosing cholangitis,” Gut, vol. 38, no. 4, pp. 610–615, 1996. View at: Google Scholar
  5. C. Y. Ponsioen, S. M. E. Vrouenraets, W. Prawirodirdjo et al., “Natural history of primary sclerosing cholangitis and prognostic value of cholangiography in a Dutch population,” Gut, vol. 51, no. 4, pp. 562–566, 2002. View at: Publisher Site | Google Scholar
  6. J. J. W. Tischendorf, P. N. Meier, C. Stabburg et al., “Characterization and clinical course of hepatobiliary carcinoma in patients with primary sclerosing cholangitis,” Scandinavian Journal of Gastroenterology, vol. 41, pp. 1227–1234, 2000. View at: Google Scholar
  7. J. J. W. Tischendorf, H. Hecker, M. Kruger, M. P. Manns, and P. N. Meier, “Characterization, outcome and prognosis in 273 patients with primary sclerosing cholangitis,” The New England Journal of Medicine, vol. 310, pp. 899–903, 1984. View at: Google Scholar
  8. R. H. Wiesner, P. M. Grambsch, E. R. Dickson et al., “Primary sclerosing cholangitis: natural history, prognostic factors and survival analysis,” Hepatology, vol. 10, no. 4, pp. 430–436, 1989. View at: Google Scholar
  9. R. Olsson, A. Danielsson, G. Jarnerot et al., “Prevalence of primary sclerosing cholangitis in patients with ulcerative colitis,” Gastroenterology, vol. 100, no. 5, pp. 1319–1323, 1991. View at: Google Scholar
  10. K. M. Abu-Elmagd, M. Malinchoc, E. R. Dickson et al., “Efficacy of hepatic transplantation in patients with primary sclerosing cholangitis,” Surgery Gynecology and Obstetrics, vol. 177, no. 4, pp. 335–344, 1993. View at: Google Scholar
  11. K. M. Abu-Elmagd, R. Selby, S. Iwatsuki et al., “Cholangiocarcinoma and sclerosing cholangitis: clinical characteristics and effect on survival after liver transplantation,” Transplantation Proceedings, vol. 25, no. 1, pp. 1124–1125, 1993. View at: Google Scholar
  12. B. Nashan, H. J. Schlitt, G. Tusch et al., “Biliary malignancies in primary sclerosing cholangitis: timing for liver transplantation,” Hepatology, vol. 23, no. 5, pp. 1105–1111, 1996. View at: Publisher Site | Google Scholar
  13. B. Brandsaeter, H. Isoneimi, U. Broome et al., “Liver transplantation for primary sclerosing cholangitis, predictors and consequences of hepatobiliary malignancy,” Journal of Hepatology, vol. 40, pp. 815–822, 2004. View at: Google Scholar
  14. R. Chapman, J. Fevery, A. Kalloo et al., “Diagnosis and management of primary sclerosing cholangitis,” Hepatology, vol. 51, no. 2, pp. 660–678, 2010. View at: Publisher Site | Google Scholar
  15. N. L. Nikolaidis, O. I. Giouleme, K. A. Tziomalos et al., “Small-duct primary sclerosing cholangitis: a single-center seven-year experience,” Digestive Diseases and Sciences, vol. 50, no. 2, pp. 324–326, 2005. View at: Publisher Site | Google Scholar
  16. A. E. Feldstein, J. Perrault, M. El-Youssif, K. D. Lindor, D. K. Freese, and P. Angulo, “Primary sclerosing cholangitis in children: a long-term follow-up study,” Hepatology, vol. 38, no. 1, pp. 210–217, 2003. View at: Publisher Site | Google Scholar
  17. G. Mieli-Vergani and D. Vergani, “Unique features of primary sclerosing cholangitis in children,” Current Opinion in Gastroenterology, vol. 26, no. 3, pp. 265–268, 2010. View at: Publisher Site | Google Scholar
  18. K. L. Cox and K. M. Cox, “Oral vancomycin: treatment of primary sclerosing cholangitis in children with inflammatory bowel disease,” Journal of Pediatric Gastroenterology and Nutrition, vol. 27, no. 5, pp. 580–583, 1998. View at: Publisher Site | Google Scholar
  19. Y. K. Davies, K. M. Cox, B. A. Abdullah, A. Safta, A. B. Terry, and K. L. Cox, “Long-term treatment of primary sclerosing cholangitis in children with oral vancomycin: an immunomodulating antibiotic,” Journal of Pediatric Gastroenterology and Nutrition, vol. 47, no. 1, pp. 61–67, 2008. View at: Publisher Site | Google Scholar
  20. M. Siedlar, A. Szczepanik, J. Wiȩckiewicz, A. Pituch-Noworolska, and M. Zembala, “Vancomycin down-regulates lipopolysaccharide-induced tumour necrosis factor alpha (TNFα) production and TNFα-mRNA accumulation in human blood monocytes,” Immunopharmacology, vol. 35, no. 3, pp. 265–271, 1997. View at: Publisher Site | Google Scholar
  21. G. Di Febo, C. Calabrese, and F. Matassoni, “New trends in non-absorbable antibiotics in gastrointestinal disease,” Italian Journal of Gastroenterology, vol. 24, no. 9, pp. 10–13, 1992. View at: Google Scholar

Copyright © 2013 Yinka K. Davies et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles