Cholangiopathies from a Pathologist‘s Perspective: The Role of Liver Biopsy in Routine Diagnostic Practice
Authors:
Ivana Jusková 1,2; Andrea Vajsová 1,3; Ondřej Fabián 1,4; Eva Sticová 1,5
Authors‘ workplace:
Pracoviště klinické a transplantační patologie, Institut klinické a experimentální medicíny, Praha
1; Ústav histologie 3. lékařské fakulty Univerzity Karlovy, Praha
2; Ústav patologie 1. lékařské fakulty Univerzity Karlovy a Všeobecné fakultní nemocnice, Praha
3; Ústav patologie a molekulární medicíny 3. lékařské fakulty Univerzity Karlovy a Fakultní Thomayerovy nemocnice, Praha
4; Ústav patologie 3. lékařské fakulty Univerzity Karlovy a Fakultní nemocnice Královské Vinohrady, Praha
5
Published in:
Čes.-slov. Patol., 61, 2025, No. 3, p. 118-134
Category:
Reviews Article
Overview
The biliary tree comprises a three-dimensional network of intrahepatic and extrahepatic ducts lined by biliary epithelium (cholangiocytes). The bile ducts and cholangiocytes may be affected by a broad spectrum of disorders collectively referred to as cholangiopathies. These conditions are classified based on anatomical aspects (predominantly affecting small or large bile ducts), aetiopathogenesis (immune-mediated, toxic and drug-induced, ischaemic, infectious, genetically determined, or neoplastic), and the predominant morphological pattern of injury (inflammatory or non-inflammatory). While abnormalities in medium-sized and large bile ducts are typically detected using radiological methods, the diagnosis of small duct cholangiopathies continues to rely primarily on histopathological evaluation of liver tissue.
This review summarises the key morphological features of the most clinically significant cholangiopathies, focusing on histopathological changes observed in liver biopsy.
Keywords:
Bile ducts – cholangitis – cholangiocytes – cholangiopathies – liver biopsy
Sources
- de Jong IEM, van den Heuvel MC, Wells RG, Porte RJ. The heterogeneity of the biliary tree. J Hepatol 2021; 75(5): 1236-1238.
- Banales JM, Huebert RC, Karlsen T, Strazzabosco M, LaRusso NF, Gores GJ. Cholangiocyte pathobiology. Nat Rev Gastroenterol Hepatol 2019; 16(5): 269-281.
- Glaser S, Francis H, Demorrow S, Lesage G, Fava G, Marzioni M, Venter J, Alpini G. Heterogeneity of the intrahepatic biliary epithelium. World J Gastroenterol 2006; 12(22): 3523-3536.
- Lazaridis KN, Strazzabosco M, Larusso NF. The cholangiopathies: disorders of biliary epithelia. Gastroenterology 2004; 127(5): 1565-1577.
- Boyer JL. Bile formation and secretion. Comprehensive Physiology. 2013;3(3):1035–1078.
- Nakanuma Y. Tutorial review for understanding of cholangiopathy. Int J Hepatol 2012; 2012 : 547840.
- Menon S, Holt A. Large-duct cholangiopathies: aetiology, diagnosis and treatment. Frontline Gastroenterol 2019; 10(3): 284-291.
- Sticova E, Fabian O. Morphological aspects of small-duct cholangiopathies: A minireview. World J Hepatol 2023; 15(4): 538-553.
- Zen Y, Hubscher SG, Nakanuma Y. Bile Duct Diseases. In: Burt AD, Ferrell LD, Hübscher SG, eds. MacSween‘s Pathology of the Liver. 7th ed. London: Elsevier; 2017 : 516-593.
- Masia R, Pratt DS, Misdraji J. A histopathologic pattern of centrilobular hepatocyte injury suggests 6-mercaptopurine-induced hepatotoxicity in patients with inflammatory bowel disease. Arch Pathol Lab Med 2012; 136(6): 618–622.
- Di Guardo G. Lipofuscin, lipofuscin-like pigments and autofluorescence. Eur J Histochem 2015; 59(1): 1–2.
- Goldfischer S, Bernstein J. Lipofuscin (aging) pigment granules of the newborn human liver. J Cell Biol 1969; 42(1): 253–261.
- Zhao J, Yue P, Mi N, et al. Biliary fibrosis is an important but neglected pathological feature in hepatobiliary disorders: from molecular mechanisms to clinical implications. Med Rev 2024; 4(4): 326-365.
- Penz-Österreicher M, Österreicher CH, Trauner M. Fibrosis in autoimmune and cholestatic liver disease. Best Pract Res Clin Gastroenterol 2011; 25(2): 245-258.
- Neuberger J, Patel J, Caldwell H, et al. Guidelines on the use of liver biopsy in clinical practice from the British Society of Gastroenterology, the Royal College of Radiologists and the Royal College of Pathology. Gut 2020;69(8): 1382-1403.
- Reau NS, Jensen DM. Vanishing bile duct syndrome. Clin Liver Dis 2008; 12(1): 203-217.
- Bessone F, Hernández N, Tanno M, Roma MG. Drug-Induced Vanishing Bile Duct Syndrome: From Pathogenesis to Diagnosis and Therapeutics. Semin Liver Dis 2021; 41(3): 331-348.
- Karlsen TH, Folseraas T, Thorburn D, Vesterhus M. Primary sclerosing cholangitis a comprehensive review. J Hepatol 2017; 67(6): 1298-1323.
- Williamson KD, Chapman RW. Primary sclerosing cholangitis: a clinical update. Br Med Bull 2015; 114(1): 53-64.
- Kim YS, Hurley EH, Park Y, Ko S. Primary sclerosing cholangitis (PSC) and inflammatory bowel disease (IBD): a condition exemplifying the crosstalk of the gut-liver axis. Exp Mol Med 2023; 55(7): 1380-1387.
- Beheshti-Maal A, Tamimi A, Iravani S, et al. PSC associated inflammatory bowel disease: a distinct entity. Expert Rev Gastroenterol Hepatol 2022; 16(2): 129-139.
- van Munster KN, Bergquist A, Ponsioen CY. Inflammatory bowel disease and primary sclerosing cholangitis: One disease or two? J Hepatol 2024; 80(1): 155-168.
- Gidwaney NG, Pawa S, Das KM. Pathogenesis and clinical spectrum of primary sclerosing cholangitis. World J Gastroenterol 2017; 23(14): 2459–2469.
- Tow CY, Chung E, Kaul B, Bhalla A, Fortune BE. Diagnostic Tests in Primary Sclerosing Cholangitis: Serology, Elastography, Imaging, and Histology. Clin Liver Dis 2024; 28(1): 157-169.
- Cazzagon N, Sarcognato S, Catanzaro E, et al. Primary Sclerosing Cholangitis: Diagnostic Criteria. Tomography 2024; 10(1): 47-65.
- Ponsioen CY. Diagnosis, Differential Diagnosis, and Epidemiology of Primary Sclerosing Cholangitis. Dig Dis 2015; 33 Suppl 2 : 134-139.
- Gardner CS, Bashir MR, Marin D, et al. Diagnostic performance of imaging criteria for distinguishing autoimmune cholangiopathy from primary sclerosing cholangitis and bile duct malignancy. Abdom Imaging 2015; 40(8): 3052-3061.
- Boberg KM, Chapman RW, Hirschfield GM, et al. Overlap syndromes: the International Autoimmune Hepatitis Group (IAIHG) position statement on a controversial issue. J Hepatol 2011; 54(2): 374-385.
- Karadag Soylu N. Histopathology of Wilson Disease. In: Liver Pathology. IntechOpen; 2021.
- Carey EJ, Ali AH, Lindor KD. Primary biliary cirrhosis. Lancet 2015; 386(10003): 1565-1575.
- Trivella J, John BV, Levy C. Primary biliary cholangitis: Epidemiology, prognosis, and treatment. Hepatol Commun 2023; 7(6): e0179.
- Shah SK, Bowlus CL. Autoimmune Markers in Primary Biliary Cholangitis. Clin Liver Dis 2024; 28(1): 93-101.
- Tanaka A, Ma X, Takahashi A, Vierling JM. Primary biliary cholangitis. Lancet 2024; 404(10457): 1053-1066.
- Tan D, Goodman ZD. Liver Biopsy in Primary Biliary Cholangitis: Indications and Interpretation. Clin Liver Dis 2018; 22(3): 579-588.
- Liu HL, Yang AY, Xiong QF, et al. Aberrant cytokeratin 7 expression by hepatocytes can predict the ductopenia grade in primary biliary cholangitis. BMC Gastroenterol 2022; 22(1): 443.
- Warnes TW, Roberts SA, Smith A, et al. Portal hypertension in primary biliary cholangitis: prevalence, natural history and histological correlates. Eur J Gastroenterol Hepatol 2021; 33(12): 1595-1602.
- Hu YF, Li SX, Liu HL, et al. Precirrhotic Primary Biliary Cholangitis with Portal Hypertension: Bile Duct Injury Correlate. Gut Liver 2024; 18(5): 867-876.
- Ludwig J, Dickson ER, McDonald GS. Staging of chronic nonsuppurative destructive cholangitis (syndrome of primary biliary cirrhosis). Virchows Arch A Pathol Anat Histopathol 1978; 379 : 103-112.
- Scheuer PJ, Lefkowitch JH. Liver biopsy interpretation. 7th ed. London: Saunders-Elsevier; 2006 : 69-84.
- Kakuda Y, Harada K, Sawada-Kitamura S, et al. Evaluation of a new histologic staging and grading system for primary biliary cirrhosis in comparison with classical systems. Hum Pathol 2013; 44(6): 1107-1117.
- Nakanuma Y, Zen Y, Harada K, et al. Application of a new histological staging and grading system for primary biliary cirrhosis to liver biopsy specimens: Interobserver agreement. Pathol Int 2010; 60(3): 167-174.
- Liang Y, Khandakar B, Hao Y, et al. Histology and clinical correlations in autoimmune hepatitis, primary biliary cholangitis, and autoimmune hepatitis-primary biliary cholangitis overlap syndrome. Ann Diagn Pathol 2023; 67 : 152178.
- Kobayashi M, Kakuda Y, Harada K, et al. Clinicopathological study of primary biliary cirrhosis with interface hepatitis compared to autoimmune hepatitis. World J Gastroenterol 2014; 20(13): 3597-3608.
- Chazouillères O. Overlap Syndromes. Dig Dis 2015; 33 Suppl 2 : 181-187.
- Sánchez-Oro R, Alonso-Muñoz EM, Martí Romero L. Review of IgG4-related disease. Gastroenterol Hepatol 2019; 42(10): 638-647.
- Vashi B, Khosroshahi A. IgG4-Related Disease with Emphasis on Its Gastrointestinal Manifestation. Gastroenterol Clin North Am 2019; 48(2): 291-305.
- Katz G, Stone JH. Clinical Perspectives on IgG4-Related Disease and Its Classification. Annu Rev Med 2022; 73 : 545-562.
- Zen Y. The Pathology of IgG4-Related Disease in the Bile Duct and Pancreas. Semin Liver Dis 2016; 36(3): 242-256.
- Lee HE, Zhang L. Immunoglobulin G4-related hepatobiliary disease. Semin Diagn Pathol 2019; 36(6): 423-433.
- Deshpande V, Zen Y, Chan JK, et al. Consensus statement on the pathology of IgG4-related disease. Mod Pathol 2012; 25(9): 1181-1192.
- Kamisawa T, Nakazawa T, Tazuma S, et al. Clinical practice guidelines for IgG4-related sclerosing cholangitis. J Hepatobiliary Pancreat Sci 2019; 26(1): 9-42.
- Tanaka A. IgG4-Related Sclerosing Cholangitis and Primary Sclerosing Cholangitis. Gut Liver 2019; 13(3): 300-307.
- Demetris AJ, Bellamy C, Hübscher SG, et al. 2016 Comprehensive Update of the Banff Working Group on Liver Allograft Pathology: Introduction of Antibody-Mediated Rejection. Am J Transplant 2016; 16(10): 2816-2835.
- Dumortier J, Conti F, Scoazec JY. Posttransplant immune-mediated cholangiopathies. Curr Opin Gastroenterol 2022; 38(2):98-103.
- Rastogi A, Nigam N, Gayatri R, et al. Biliary Epithelial Senescence in Cellular Rejection Following Live Donor Liver Transplantation. J Clin Exp Hepatol 2022; 12(6): 1420-1427.
- Trussoni CE, O‘Hara SP, LaRusso NF. Cellular senescence in the cholangiopathies: a driver of immunopathology and a novel therapeutic target. Semin Immunopathol 2022; 44(4):527-544.
- Quaglia A, Duarte R, Patch D, et al. Histopathology of graft versus host disease of the liver. Histopathology 2007; 50(6): 727-738.
- Chiba T, Yokosuka O, Goto S, et al. Clinicopathological features in patients with hepatic graft-versus-host disease. Hepatogastroenterology 2005; 52(66): 1849-1853.
- Jain R, Yadav D, Puranik N, et al. Sarcoidosis: Causes, Diagnosis, Clinical Features, and Treatments. J Clin Med 2020; 9(4): 1081.
- Nicolosi S, Chernovsky M, Angoni D, et al. Gastrointestinal Manifestations of Sarcoidosis: A State-of-the-Art, Comprehensive Review of the Literature-Practical Clinical Insights and Many Unmet Needs on Diagnosis and Treatment. Pharmaceuticals (Basel) 2024; 17(9): 1106.
- Rossi G, Ziol M, Roulot D, et al. Hepatic Sarcoidosis: Current Concepts and Treatments. Semin Respir Crit Care Med 2020; 41(5): 652-658.
- Chen C, Luo N, Dai F, et al. Advance in pathogenesis of sarcoidosis: Triggers and progression. Heliyon 2024; 10(5): e27612.
- Miedema J, Cinetto F, Smed-Sörensen A, Spagnolo P. The immunopathogenesis of sarcoidosis. J Autoimmun 2024; 103247.
- Kahi CJ, Saxena R, Temkit M, et al. Hepatobiliary disease in sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 2006; 23(2): 117-123.
- Tana C, Donatiello I, Caputo A, et al. Clinical Features, Histopathology and Differential Diagnosis of Sarcoidosis. Cells 2021; 11(1): 59.
- Kumar SN, Prasad TS, Narayan PA, Muruganandhan J. Granuloma with langhans giant cells: An overview. J Oral Maxillofac Pathol 2013; 17(3): 420-423.
- Valeyre D, Brauner M, Bernaudin JF, et al. Differential diagnosis of pulmonary sarcoidosis: a review. Front Med (Lausanne) 2023; 10 : 1150751.
- Visentin M, Lenggenhager D, Gai Z, Kullak-Ublick GA. Drug-induced bile duct injury. Biochim Biophys Acta Mol Basis Dis 2018; 1864(4): 1498-1506.
- Salas-Silva S, Simoni-Nieves A, Lopez-Ramirez J, et al. Cholangiocyte death in ductopenic cholestatic cholangiopathies: Mechanistic basis and emerging therapeutic strategies. Life Sci 2019; 218 : 324-339.
- Scoazec JY. Drug-induced bile duct injury: new agents, new mechanisms. Curr Opin Gastroenterol 2022; 38(2): 83-88.
- LiverTox. Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012. Available from: https://www.ncbi.nlm.nih. gov/books/NBK547852/
- Zen Y, Yeh MM. Hepatotoxicity of immune checkpoint inhibitors: a histology study of seven cases in comparison with autoimmune hepatitis and idiosyncratic drug-induced liver injury. Mod Pathol 2018; 31(6): 965-973.
- Zen Y, Yeh MM. Checkpoint inhibitor-induced liver injury: A novel form of liver disease emerging in the era of cancer immunotherapy. Semin Diagn Pathol 2019; 36(6): 434-440.
- Zen Y, Chen YY, Jeng YM, et al. Immune-related adverse reactions in the hepatobiliary system: second-generation check-point inhibitors highlight diverse histological changes. Histopathology 2020; 76(3): 470-480.
- Shatila M, Zhang HC, Shirwaikar Thomas A, et al. Systematic review of immune checkpoint inhibitor-related gastrointestinal, hepatobiliary, and pancreatic adverse events. J Immunother Cancer 2024; 12(11): e009742.
- Velayudham LS, Farrell GC. Drug-induced cholestasis. Expert Opin Drug Saf 2003; 2(3): 287-304.
- Kubitz R, Dröge C, Kluge S, et al. Genetic variations of bile salt transporters. Drug Discov Today Technol 2014; 12: e55-67.
- Vitale G, Mattiaccio A, Conti A, et al. Molecular and Clinical Links between Drug-Induced Cholestasis and Familial Intrahepatic Cholestasis. Int J Mol Sci 2023; 24(6): 5823.
- Luo Z, Jegga AG, Bezerra JA. Gene-disease associations identify a connectome with shared molecular pathways in human cholangiopathies. Hepatology 2018; 67(2): 676-689.
- Fabris L, Fiorotto R, Spirli C, et al. Pathobiology of inherited biliary diseases: a roadmap to understand acquired liver diseases. Nat Rev Gastroenterol Hepatol 2019; 16(8): 497-511.
- Drenth JP, Chrispijn M, Bergmann C. Congenital fibrocystic liver diseases. Best Pract Res Clin Gastroenterol 2010; 24(5): 573-584.
- Hellen DJ, Karpen SJ. Genetic Contributions to Biliary Atresia: A Developmental Cholangiopathy. Semin Liver Dis 2023; 43(3): 323-335.
- Wood W, Tinich T, Lazar L, Schooler GR, Sathe M. Cystic fibrosis hepatobiliary involvement: an update on imaging in diagnosis and monitoring. Pediatr Radiol 2024; 54(9): 1416-1427.
- Hadchouel M, Gautier M. Histopathologic study of the liver in the early cholestatic phase of alpha-1-antitrypsin deficiency. J Pediatr 1976; 89(2): 211-215.
- Desmet VJ. Ludwig symposium on biliary disorders--part I. Pathogenesis of ductal plate abnormalities. Mayo Clin Proc 1998; 73(1): 80–89.
- Desmet VJ. Congenital diseases of intrahepatic bile ducts: variations on the theme “ductal plate malformation.” Hepatology 1992; 16(4): 1069–1083.
- Kothari TH, Khara SS, Kothari DB, Schiano T. Caroli Disease. Consultant 2024; 48(5): 391.
- Hildebrandt F, Benzing T, Katsanis N. Ciliopathies. N Engl J Med 2011; 364(16): 1533-1543.
- Gunay-Aygun M. Liver and kidney disease in ciliopathies. Am J Med Genet C Semin Med Genet 2009; 151C(4): 296-306.
- Perugorria MJ, Bujanda L, Banales JM. More insight into the diversity of cholangiocyte ciliopathies. J Hepatol 2016; 65(6): 1083-1085.
- Kotha S, Berry P. Hepatic, pancreatic and renal manifestations of a ciliopathy. Hepatobiliary Pancreat Dis Int 2021; 20(4): 394-395.
- Roediger R, Dieterich D, Chanumolu P, et al. Polycystic Kidney/Liver Disease. Clin Liver Dis 2022; 26(2): 229-243.
- Antala S, Taylor SA. Biliary Atresia in Children: Update on Disease Mechanism, Therapies, and Patient Outcomes. Clin Liver Dis 2022; 26(3): 341-354.
- Quelhas P, Cerski C, Dos Santos JL. Update on Etiology and Pathogenesis of Biliary Atresia. Curr Pediatr Rev 2022; 19(1): 48-67.
- Davenport M, Gonde C, Redkar R, et al. Immunohistochemistry of the liver and biliary tree in extrahepatic biliary atresia. J Pediatr Surg 2001; 36(7): 1017-1025.
- Muthukanagarajan SJ, Karnan I, Srinivasan P, et al. Diagnostic and Prognostic Significance of Various Histopathological Features in Extrahepatic Biliary Atresia. J Clin Diagn Res 2016; 10(6): EC23-27.
- Vij M, Rela M. Biliary atresia: pathology, etiology and pathogenesis. Future Sci OA 2020; 6(5): FSO466.
- Higashio A, Yoshioka T, Kanamori Y, et al. Relationships Between Histopathological Findings in the Liver and Prognosis in Patients With Biliary Atresia. Clin Pathol 2022; 15 : 2632010X221132686.
- Kohut TJ, Gilbert MA, Loomes KM. Alagille Syndrome: A Focused Review on Clinical Features, Genetics, and Treatment. Semin Liver Dis 2021; 41(4): 525-537.
- Mašek J, Andersson ER. Jagged-mediated development and disease: Mechanistic insights and therapeutic implications for Alagille syndrome. Curr Opin Cell Biol 2024; 86 : 102302.
- Spinner NB, Loomes KM, Krantz ID, et al. Alagille Syndrome. In: Adam MP, Feldman J, Mirzaa GM, et al., eds. GeneReviews®. Seattle: University of Washington; 1993-2024.
- Herman HK, Abramowsky CR, Caltharp S, et al. Identification of Bile Duct Paucity in Alagille Syndrome: Using CK7 and EMA Immunohistochemistry as a Reliable Panel for Accurate Diagnosis. Pediatr Dev Pathol 2016; 19(1): 47-50.
- Gilbert MA, Loomes KM. Alagille syndrome and non-syndromic paucity of the intrahepatic bile ducts. Transl Gastroenterol Hepatol 2021; 6 : 22.
- Reichert MC, Lammert F. ABCB4 Gene Aberrations in Human Liver Disease: An Evolving Spectrum. Semin Liver Dis 2018; 38(4): 299-307.
- Sticova E, Jirsa M. ABCB4 disease: Many faces of one gene deficiency. Ann Hepatol 2020; 19(2): 126-133.
- Stättermayer AF, Halilbasic E, Wrba F, et al. Variants in ABCB4 (MDR3) across the spectrum of cholestatic liver diseases in adults. J Hepatol 2020; 73(3): 651-663.
- Hegarty R, Gurra O, Tarawally J, et al. Clinical outcomes of ABCB4 heterozygosity in infants and children with cholestatic liver disease. J Pediatr Gastroenterol Nutr 2024; 78(2): 339-349.
- Frider B, Castillo A, Gordo-Gilart R, et al. Reversal of advanced fibrosis after long-term ursodeoxycholic acid therapy in a patient with residual expression of MDR3. Ann Hepatol 2015; 14(5): 745-751.
- Morotti RA, Suchy FJ, Magid MS. Progressive familial intrahepatic cholestasis (PFIC) type 1, 2, and 3: a review of the liver pathology findings. Semin Liver Dis 2011; 31(1): 3-10.
- Girard M, Bizet AA, Lachaux A, et al. DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis. Hum Mutat 2016; 37(10): 1025-1029.
- Grammatikopoulos T, Sambrotta M, Strautnieks S, et al. Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis. J Hepatol 2016; 65(6): 1179-1187.
- Stanca CM, Fiel MI, Kontorinis N, et al. Chronic ductopenic rejection in patients with recurrent hepatitis C virus treated with pegylated interferon alfa-2a and ribavirin. Transplantation 2007; 84(2): 180-186.
- Dhingra S, Ward SC, Thung SN. Liver pathology of hepatitis C, beyond grading and staging of the disease. World J Gastroenterol 2016; 22(4): 1357-1366.
- Li Y, Ayata G, Baker SP, Banner BF. Cholangitis: a histologic classification based on patterns of injury in liver biopsies. Pathol Res Pract 2005; 201(8–9): 565–572.
- Uno S, Hase R, Kobayashi M, Shiratori T, Nakaji S, Hirata N, et al. Short-course antimicrobial treatment for acute cholangitis with Gram-negative bacillary bacteremia. Int J Infect Dis 2017; 55 : 81–85.
- Miura F, Takada T, Kawarada Y, Nimura Y, Wada K, Hirota M, et al. Flowcharts for the diagnosis and treatment of acute cholangitis and cholecystitis: Tokyo Guidelines. J Hepatobiliary Pancreat Surg 2007; 14(1): 27–34.
- Tonolini M, Bianco R. HIV-related/AIDS cholangiopathy: pictorial review with emphasis on MRCP findings and differential diagnosis. Clin Imaging 2013; 37(2): 219-226.
- Naseer M, Dailey FE, Juboori AA, et al. Epidemiology, determinants, and management of AIDS cholangiopathy: A review. World J Gastroenterol 2018; 24(7): 767-774.
- Alsharif NM, Souleiman MM, Gunaseelan L, et al. AIDS-Associated Cryptosporidial and Cytomegalovirus Cholangiopathy. Cureus 2024; 16(7): e63963.
- Da Cunha T, Wu GY. Cytomegalovirus hepatitis in immunocompetent and immunocompromised hosts. J Clin Transl Hepatol 2021; 9(1): 106–115.
- Demetris AJ, Jaffe R, Starzl TE. A review of adult and pediatric post-transplant liver pathology. Pathol Annu 1987; 22(Pt 2): 347–386.
- Roth NC, Kim A, Vitkovski T, et al. Post-COVID-19 Cholangiopathy: A Novel Entity. Am J Gastroenterol 2021; 116(5): 1077-1082.
- Yadlapati S, Jarrett SA, Baik D, et al. COVID-19 related biliary injury: A review of recent literature. World J Gastroenterol 2023; 29(14): 2127-2133.
- Veerankutty FH, Sengupta K, Vij M, et al. Post-COVID-19 cholangiopathy: Current understanding and management options. World J Gastrointest Surg 2023; 15(5): 788-798.
- Borges VFA, Cotrim HP, Andrade ARCF, et al. COVID-19-Related Cholangiopathy: Histological Findings. Diagnostics (Basel) 2024; 14(16): 1804.
- Deltenre P, Valla DC. Ischemic cholangiopathy. Semin Liver Dis 2008; 28(3): 235-246.
- Buis CI, Hoekstra H, Verdonk RC, et al. Causes and consequences of ischemic-type biliary lesions after liver transplantation. J Hepatobiliary Pancreat Surg 2006; 13(6): 517-524.
- Goria O, Archambeaud I, Lemaitre C, et al. Ischemic cholangiopathy: An update. Clin Res Hepatol Gastroenterol 2020; 44(4): 486-490.
- Gudnason HO, Björnsson ES. Secondary sclerosing cholangitis in critically ill patients: current perspectives. Clin Exp Gastroenterol 2017; 10 : 105-111.
- Martins P, Verdelho Machado M. Secondary Sclerosing Cholangitis in Critically Ill Patients: An Underdiagnosed Entity. GE Port J Gastroenterol 2020; 27(2): 103-114.
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