Skip to main content
Log in

Clinical, histologic, and immunopathologic features of primary biliary cirrhosis

  • Published:
Springer Seminars in Immunopathology Aims and scope Submit manuscript

Conclusions

This review of clinical and morphologic features of PBC deals with four processes in the evolution of the disease: (1) etiologic and predisposing features; (2) injury of bile ducts and secondarily of hepatocytes; (3) precholestasis and cholestasis; and (4) hepatic derangement not of a biliary nature. It further refers to four stages in the evolution of PBC — ductal, ductular, scarring, and cirrhotic stage — with extensive transitions between each other and recurrence of previous stages in later ones. Probably a different immunologic process is responsible for the initial and continuing bile duct injury and for a secondary “hepatitic” component as well as for the periductular fibrosis. The further evolution of PBC, however, appears to be dominated by the cholestatic consequences of mechanical fibrotic interference with biliary secretion, mainly in the periportal area. Assisted by progression of the “ hepatitic” process, it results to varying degrees in destruction of the hepatic architecture, potentially terminating in cirrhosis. But PBC is not a primary cholestatic disease; frank cholestasis is clinically and histologically a relatively late phenomenon in a disease still mysterious and with a potentially long evolution. Cirrhosis, which is the conventional name of the disease, is only present or even in development during a short terminal fraction of the total life span of the disease.

Although PBC is a relatively rare disease, even if now more readily recognized, it nevertheless serves as a useful experiment of nature for clarifying the pathology of liver disease in general and its immunologic aspects in particular.

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.

Similar content being viewed by others

References

  1. Ahrens EH, Payne MA, Kunkel HG, Eisenmenger WJ, Blondheim, SJ (1950) Primary biliary cirrhosis. Medicine 29: 299

    PubMed  Google Scholar 

  2. Alarcon-Segovia D, Diaz-Jouanen E, Fishbein E, (1974) Features of Sjögren's syndrome in primary biliary cirrhosis. Ann Intern Med 79: 31

    Google Scholar 

  3. Baggenstoss AH, Foukd WT, Butt HR, Bahn RC (1964) The pathology of primary biliary cirrhosis with emphasis on histogenesis. Am J Clin Pathol 42: 259

    PubMed  Google Scholar 

  4. Baggenstoss AH, Soloway RD, Summerskill WHJ, Elveback LR, Schoenfield LJ (1972) Chronic active liver disease: The range of histologic lesions, their response to treatment and evolution. Hum Pathol 3: 183

    PubMed  Google Scholar 

  5. Bagheri SA, Bolt MG, Boyer JL, Palmer RH (1978) Stimulation of thymidine incorporation in mouse liver and biliary tract epithelium by lithocholate and deoxycholate. Gastroenterology 74: 188

    PubMed  Google Scholar 

  6. Bermann MD, Rabin L, O'Donnell J, Gratwohl AA, Graw RG Jr, Deisseroth AB, Jones EA (1980) The liver in long-term survivors of marrow transplant — chronic graft-versus-host disease. J Clin Gastroenterol 2: 53

    PubMed  Google Scholar 

  7. Bloomer JR, Allen RM, Klatskin G (1976) Serum bile acids in primary biliary cirrhosis. Arch Intern Med 136: 57

    PubMed  Google Scholar 

  8. Bodenheimer HC Jr, Schaffner F (1979) Primary biliary cirrhosis and the immune system. Am J Gastroenterol 72: 285

    PubMed  Google Scholar 

  9. Chamuleay RAFM, Van Berge Henegouwen GP, Bronkhorst FB, Brandt KH (1975) Primary biliary cirrhosis in sisters. Neth J Med 18: 170

    PubMed  Google Scholar 

  10. Chedid A, Spellberg MA, DeBeer RA (1974) Ultrastructural aspects of primary biliary cirrhosis and other types of cholestatic liver disease. Gastroenterology 7: 858

    Google Scholar 

  11. Child DL, Mathews JA, Thompson RPH (1977) Arthritis and primary biliary cirrhosis. Br Med J 2: 557

    Google Scholar 

  12. Chohan MR (1973) Primary biliary cirrhosis in twin sisters. Gut 14: 213

    PubMed  Google Scholar 

  13. Christensen E, Crowe J, Doniach D, Popper H, Ranek L, Rodes J, Tygstrup N, Williams R (1980) Clinical pattern and course of disease in primary biliary cirrhosis based on analysis of 236 patients. Gastroenterology 78: 236

    PubMed  Google Scholar 

  14. Crowe J, Christensen E, Smith M, Cochrane M, Ranek L, Watkinson G, Doniach D, Popper H, Tygstrup N, Williams R (1980) Azathioprine in primary biliary cirrhosis; A preliminary report of an international trial. Gastroenterology 78: 1005

    PubMed  Google Scholar 

  15. Crowe JP, Christensen E, Butler J, Wheeler P, Doniach D, Keenan J, Williams R (1980) Primary biliary cirrhosis: The prevalence of hypothyroidism and its relationship to thyroid autoantibodies and Sicca syndrome. Gastroenterology 78: 1437

    PubMed  Google Scholar 

  16. Denk H, Franke WW, Eckerstorfer R, Schmid E, Kerjaschki D (1979) Formation and involution of Mallory bodies (“alcoholic hyalin”) in murine and human liver revealed by immunofluorescence microscopy with antibodies to prekeratin. Proc Natl Acad Sci USA 76: 4112

    PubMed  Google Scholar 

  17. Dickson ER, Fleming RC, Ludwig J (1979) Primary biliary cirrhosis. In: Popper H, Schaffner F (eds) Progress in liver diseases, vol VI. Grune and Stratton, New York, p 487

    Google Scholar 

  18. Douglas JG, Finlayson NDC (1979) Are increased individual susceptibility and environmental factors both necessary for the development of primary biliary cirrhosis? Br Med J II: 419

    Google Scholar 

  19. Eppinger H, Kaunitz H, Popper H (1935) Die seriöse Entzuendung. Eine Permeabilitäts-Pathologie. Springer, Wien, p 145

    Google Scholar 

  20. Epstein O, Arborgh B, Wroblewski R, Saciv M, Scheuer PJ, Sherlock S (1979) Is copper hepatotoxic in primary biliary cirrhosis? Gastroenterology 77: A10

    Google Scholar 

  21. Epstein P, Thomas HC, Sherlock S (1980) Primary biliary cirrhosis is a “dry gland” syndrome with features of chronic graft versus host (GVH) disease. Lancet I: 1166

    Google Scholar 

  22. Ercilla G, Pares A, Arriaga F, Bruguera M, Castillo R, Rodes J, Vives J (1979) Primary biliary cirrhosis associated with HLA-DRw3. Tissue Antigens 14: 449

    PubMed  Google Scholar 

  23. Fee HJ, Gewirtz H, Schiller J, Longmire WP (1977) Sclerosing cholangitis and primary biliary cirrhosis — a disease spectrum? Ann Surg 186: 589

    PubMed  Google Scholar 

  24. Fox RA, James DG, Scheuer PJ, Sharma O, Sherlock S (1969) Impaired delayed hypersensitivity in primary biliary cirrhosis. Lancet I: 959

    Google Scholar 

  25. Fox RA, Scheuer PJ, Sherlock S (1973) Asymptomatic primary biliary cirrhosis. Gut 14: 444

    PubMed  Google Scholar 

  26. Galbraith RM, Eddleston ALWF, Smith MGM, Williams R, McSween RNM, Watkinson G, Dick H, Kennedy LA, Batchelor JR (1974) Histocompatibility antigens in active chronic hepatitis and primary biliary cirrhosis. Br Med J. II: 604

    Google Scholar 

  27. Galbraith RM, Smith M, Mackenzie RM, Tee DE, Doniach D, Williams R (1974) High prevalence of seroimmunologic abnormalities in relatives of patients with active chronic hepatitis or primary biliary cirrhosis. N Engl J Med 290: 63

    PubMed  Google Scholar 

  28. Gerber MA, Orr W, Denk H, Schaffner F, Popper H (1973) Hepatocellular hyalin in cholestasis and cirrhosis: Its diagnostic significance. Gastroenterology 63: 89

    Google Scholar 

  29. Geubel AP, Baggenstoss AH, Summerskill WHJ (1976) Response to treatment can differentiate chronic active liver disease with cholangitic features from the primary biliary cirrhosis syndrome. Gastroenterology 71: 444

    PubMed  Google Scholar 

  30. Ghent CN, Bloomer JR, Klatskin G (1977) Elevations in skin tissue levels of bile acids in human cholestasis: Relation to serum levels and to pruritus. Gastroenterology 73: 1125

    PubMed  Google Scholar 

  31. Glober GA, Wilkerson JA (1968) Biliary cirrhosis following the administration of methyltestosterone. JAMA 204: 170

    PubMed  Google Scholar 

  32. Goldfischer S, Popper H, Sternlieb I (1980) The Significance of variations in the distribution of copper in liver disease. Am J Pathol 99: 715

    PubMed  Google Scholar 

  33. Golding PL, Bown R, Mason AMS, Taylor E (1970) “Sicca complex” in liver disease. Br Med J II: 340

    Google Scholar 

  34. Golding PL, Mason AMS (1971) Renal tubular acidosis and autoimmune liver disease. Gut 12: 153

    PubMed  Google Scholar 

  35. Hanger FM, Gutman AB (1940) Postarsphenamine jaundice apparently due to obstruction of intrahepatic biliary tract. JAMA 115: 263

    Google Scholar 

  36. Hanik L, Eriksson S (1977) Presymptomatic primary biliary cirrhosis. Acta Med Scand 202: 277

    PubMed  Google Scholar 

  37. Henning HV, Vogel HM, Ihlenfeld J, Buchegger K, Luders CJ (1975) Leberschaden unter N-propylajmalin-bitartrat (NPAB). Z Gastroenterol 13: 501

    PubMed  Google Scholar 

  38. Herlong HF, Russel RM, Garrett M, Maddrey WC (1979) Vitamin A deficiency in primary biliary cirrhosis: An additional role for zinc. Gastroenterology 77: A16

    Google Scholar 

  39. Ishak KC, Irey NS (1972) Hepatic injury associated with the phenothiazines: Clinicopathologic and follow-up study of 36 patients. Arch Pathol 93: 283

    PubMed  Google Scholar 

  40. Jain S, Scheuer PJ, Samourian S, McGee JO D, Sherlock S (1977) A controlled trial of D-penicillamine therapy in primary biliary cirrhosis. Lancet I: 831

    Google Scholar 

  41. Jones WA, Tisdale WA (1963) Posthepatitic cirrhosis clinically simulating biliary obstruction (so-called primary biliary cirrhosis). N Engl J Med 268: 629

    Google Scholar 

  42. Kerr JFR, Cooksley WGE, Searle J, Halliday JW, Halliday WJ, Holder L, Roberts I, Burnett W, Powell LW (1979) The nature of piecemeal necrosis in chronic active hepatitis. Lancet II: 827

    Google Scholar 

  43. Kew MC, Varma RR, Dos Santos HA, Scheuer PJ, Sherlock S (1971) Portal hypertension in primary biliary cirrhosis. Gut 12: 830

    PubMed  Google Scholar 

  44. Klion FM, Schaffner F (1966) Electron microscopic observations in primary biliary cirrhosis. Arch Pathol 81: 152

    PubMed  Google Scholar 

  45. Klöppel G, Seifert G, Lindner H, Dammermann R, Sack HJ, Berg PA (1977) Histopathological features in mixed types of chronic aggressive hepatitis and primary biliary cirrhosis: Correlation of liver histology with mitochondrial antibodies of different specificity. Virchows Arch [Pathol Anat] 373; 143

    Google Scholar 

  46. Klouda PT, Mamos J, Acheson EJ, Dyer PA, Goldby FS, Harris R, Lawler W, Mallick NP, Williams G (1979) Strong association between idiopathic membranous nephropathy and HLA-DRW3. Lancet II: 770

    Google Scholar 

  47. Krasner N, Johnson PJ, Portmann B, Watkinson RN, MacSween M, Williams R (1979) Hepatocellular carcinoma in primary biliary cirrhosis: Report of four cases. Gut 20: 255

    PubMed  Google Scholar 

  48. Krawitt EL, Grundman MJ, Mawer EB (1977) Absorption, hydroxylation, and excretion of vitamin D, in primary biliary cirrhosis. Lancet II: 17

    Google Scholar 

  49. LaBreque DR, Klatskin G (1980) The various histopathologic presentations of sclerosing cholangitis. Gastroenterology 78: 1310

    Google Scholar 

  50. Landing BH (1974) Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst — the concept of infantile obstructive cholangiopathy. Prog Pediatr Surg 6: 113

    PubMed  Google Scholar 

  51. Lebrec D, Sicot C, Degott C, Benhamou JP (1976) Portal hypertension and primary biliary cirrhosis. Digestion 14: 220

    PubMed  Google Scholar 

  52. Legge DA, Carlson HC, Dickson ER, Ludwig J (1971) Cholangiographic findings in cholangiolitic hepatitis: Syndrome of primary biliary cirrhosis. Am J Roentgenol 113: 16

    Google Scholar 

  53. Levy VG, Opolon P, Caroli J (1964) Cirrhoses biliaires primitives. Contribution au diagnostic. Etude anatomopathologique par la méthode de reconstruction. Sem Hop Paris 40: 1749

    PubMed  Google Scholar 

  54. Logan RFA, Ferguson A, Finlayson NDC, Weir DG (1978) Primary biliary cirrhosis and coeliac disease: An association? Lancet I: 4

    Google Scholar 

  55. Long RG, Scheuer PJ, Sherlock S (1977) Presentation and course of asymptomatic primary biliary cirrhosis. Gastroenterology 72: 1204

    PubMed  Google Scholar 

  56. Long RG, Varghese Z, Meinhard EA, Skinner RK, Wills MR, Sherlock S (1978) Parenteral 1,25-dihydroxycholecalciferol in hepatic osteomalacia. Br Med J I: 75

    Google Scholar 

  57. Ludwig J, Dickson ER, McDonald GSA (1978) Staging of chronic nonsuppurative destructive cholangitis (syndrome of primary biliary cirrhosis) Virchows Arch [Pathol Anat] 379: 103

    Google Scholar 

  58. Ludwig J, McDonald GSA, Dickson ER, Elveback LR, McGall JT (1979) Copper stains and the syndrome of primary cirrhosis: Evaluation of staining methods and their usefulness for diagnosis and trials of penicillamine treatment. Arch Pathol Lab Med 103: 467

    PubMed  Google Scholar 

  59. MacSween RNM (1973) Mallory's (“alcoholic”) hyalin in primary biliary cirrhosis. J Clin Pathol 26: 340

    PubMed  Google Scholar 

  60. Marx WJ, O'Connell DJ (1979) Arthritis of primary biliary cirrhosis. Arch Intern Med 139: 213

    PubMed  Google Scholar 

  61. Matsuda Y, Baraona E, Salaspuro M, Lieber CS (1979) Effects of ethanol on liver microtubules and Golgi apparatus. Possible role in altered hepatic secretion of plasma proteins. Lab Invest 41: 455

    PubMed  Google Scholar 

  62. Miller F, Lane B, Soterakis J, D'Angelo WA (1979) Primary biliary cirrhosis and scleroderma. Arch Pathol Lab Med 103: 505

    PubMed  Google Scholar 

  63. Murray-Lyon IM, Thompson RPH, Ansell ID, Williams R (1970) Scleroderma and primary biliary cirrhosis. Br Med J III: 258

    Google Scholar 

  64. Nakanuma Y, Karino T, Ohta G (1979) Orcein positive granules in the hepatocytes in chronic intrathepatic cholestasis. Virchows Arch [Pathol Anat] 382: 21

    Google Scholar 

  65. Nakanuma Y, Ohta G (1979) Histometric and serial section observations of the intrahepatic bile ducts in primary biliary cirrhosis. Gastroenterology 76: 1326

    PubMed  Google Scholar 

  66. Paronetto F, Popper H (1976) Hetero-iso- and autoimmune phenomena in the liver. In: Miescher PA, Müller-Eberhard HJ (eds) Textbook of immunopathology, vol 2. Grune and Stratton, New York, p 789

    Google Scholar 

  67. Popper H (1978) The problem of histologic evaluation of primary biliary cirrhosis. Virchows Arch [Pathol Anat] 379: 99

    Google Scholar 

  68. Popper H, Schaffner F (1970) Pathophysiology of cholestasis. Hum Pathol 1: 1

    PubMed  Google Scholar 

  69. Popper H, Schaffner F (1970) Nonsuppurative destructive chronic cholangitis and chronic hepatitis In: Popper H, Schaffner F (eds) Progress in liver diseases, vol III. Grune and Stratton, New York, p 336

    Google Scholar 

  70. Potter BJ, Elias E, Jones EA (1976) Hypercatabolism of the third component of complement in patients with primary biliary cirrhosis. J Lab Clin Med 88: 427

    PubMed  Google Scholar 

  71. Potter BJ, Elias E, Thomas HC, Sherlock S (1980) Complement metabolism in chronic liver disease. Catabolism of Clq in chronic active liver disease and primary biliary cirrhosis. Gastroenterology 78: 1034

    PubMed  Google Scholar 

  72. Poulsen H, Christoffersen P (1972) Abnormal bile duct epithelium in chronic aggressive hepatitis and cirrhosis: A review of morphology and clinical, biochemical, and immunologic features. Hum Pathol 3: 217

    PubMed  Google Scholar 

  73. Read AE, Harrison CV, Sherlock S (1961) Chronic chlorpromazine jaundice: With particular reference to its relationship to primary biliary cirrhosis. Am J Med 31: 249

    PubMed  Google Scholar 

  74. Reed JS, Meredith SC, Nemchausky BA, Rosenberg IH, Boyer JL (1980) Bone disease in primary biliary cirrhosis: Reversal of osteomalacia with oral 25-hydroxyvitamin D. Gastroenterology 78: 512

    PubMed  Google Scholar 

  75. Reynolds TB, Denison EK, Frankl HD, Liebermann FL, Peters RL (1971) Primary biliary cirrhosis with scleroderma, Raynaud's phenomenon and telangiectasia. Am J Med 50: 302

    PubMed  Google Scholar 

  76. Riemann JF, Schmidt H, Zimmermann W (1979) Frühveränderungen bei chronisch-destruktiver, nicht eitriger Cholangitis. Z Gastroenterol 17: 617

    Google Scholar 

  77. Rubin E, Schaffner F, Popper H (1965) Primary biliary cirrhosis. Chronic nonsuppurative destructive cholangitis. Am J Pathol 46: 387

    PubMed  Google Scholar 

  78. Rudzki C, Ishak KG, Zimmerman HJ (1975) Chronic intrahepatic cholestasis of sarcoidosis. Am J Med 59: 373

    PubMed  Google Scholar 

  79. Salaspuro MP, Sipponen P, Ikkala E, Kolho L, Makkonen HM, Miettinen TA, Räsänen JA, Siurala M (1976) Clinical correlations and significance of orcein positivity in chronic active hepatitis and primary biliary cirrhosis. Ann Clin Res 8: 206

    PubMed  Google Scholar 

  80. Schaffner F (1975) Primary biliary cirrhosis. Clin Gastroenterol 4: 351

    PubMed  Google Scholar 

  81. Scheuer PJ (1973) Liver biopsy interpretation. Williams and Wilkins, Baltimore, p 33

    Google Scholar 

  82. Shapiro JM, Smith H, Schaffner F (1979) Serum bilirubin: A prognostic factor in primary biliary cirrhosis. Gut 20: 137

    PubMed  Google Scholar 

  83. Sherlock S (1976) Primary biliary cirrhosis. In: Popper H, Schaffner F (eds) Progress in liver diseases, vol. V Grune and Stratton, New York, p 559

    Google Scholar 

  84. Sipponen P (1976) Orcein positive hepatocellular material in long-standing biliary diseases. I. Histochemical characteristics. Scand J Gastroenterol 11: 545

    PubMed  Google Scholar 

  85. Sipponen P (1976) Orcein positive hepatocellular material in long-standing biliary diseases. II. Ultrastructural studies. Scand J Gastroenterol 11: 553

    PubMed  Google Scholar 

  86. Sipponen P, Salaspuro MP, Makkonen HM (1975) Orcein positive hepatocellular material in histological diagnosis of primary biliary cirrhosis. Ann Clin Res 7: 273

    PubMed  Google Scholar 

  87. Stanley NN, Fox RA, Whimster WF, Sherlock S, James GD (1972) Primary biliary cirrhosis or sarcoidosis — or both. N Engl J Med 287: 1282

    PubMed  Google Scholar 

  88. Summerfield JA, Elias E, Dick R, Sherlock S (1974) The biliary system in primary biliary cirrhosis. A study by endoscopic retrograde cholangiopancreatography. Digestion 10: 381

    Google Scholar 

  89. Thomas HC, Potter BJ, Sherlock S (1977) Is primary biliary cirrhosis an immune complex disease? Lancet II: 1261

    Google Scholar 

  90. Tong MJ, Nies KM, Reynolds TB, Quismorio FP (1976) Immunological studies in familial primary biliary cirrhosis. Gastroenterology 71: 305

    PubMed  Google Scholar 

  91. Wiesner RH, Barham SS, Dickson ER (1980) Hepatic copper: Elevation, subcellular distribution, and progression of primary biliary cirrhosis. Gastroenterology 78: 1326

    Google Scholar 

  92. Zeegen R, Stansfeld AG, Dawson AM, Hunt AH (1969) Bleeding oesophageal varices as the presenting feature in primary biliary cirrhosis. Lancet II: 9

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Original observations were supported in part by National Institutes of Health, National Institute of Environmental Health Sciences Grant No. 2 P30 E500928 06

Rights and permissions

Reprints and permissions

About this article

Cite this article

Popper, H., Paronetto, F. Clinical, histologic, and immunopathologic features of primary biliary cirrhosis. Springer Semin Immunopathol 3, 339–354 (1980). https://doi.org/10.1007/BF02054109

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02054109

Keywords

Navigation