
/* Sequence of slide descriptions */
desc1  = 'Slide 1  </font><br><font id=italictext>Primary Biliary Cirrhosis</font><br><font id=normaltext>                                                      A damaged medium-sized interlobular bile duct is surrounded by a dense mononuclear inflammatory infiltrate.  Lymphocytes focally infiltrate bile duct epithelium.                                                                                                                                                                                                                                              ';
desc2  = 'Slide 2  </font><br><font id=italictext>Primary Biliary Cirrhosis, Florid Duct Lesion</font><br><font id=normaltext>                                  Granulomatous destruction of bile ducts is a characteristic histologic hallmark of primary biliary cirrhosis, although granulomas are not seen in all cases and may be absent in late stages. Epithelioid macrophages may be loosely grouped in ill defined clusters or may form a sarcoid-like granuloma, as shown here.                                                                                      ';
desc3  = 'Slide 3  </font><br><font id=italictext>Primary Biliary Cirrhosis, Florid Duct Lesion</font><br><font id=normaltext>                                  The bile duct epithelium shows degenerative changes such as vacuolization and cytoplasmic granularity.                                                                                                                                                                                                                                                                                                         ';
desc4  = 'Slide 4  </font><br><font id=italictext>Primary Sclerosing Cholangitis</font><br><font id=normaltext>                                                 Concentric periductal "onion-skinning" fibrosis with atrophy and injury to bile duct epithelium is the classic lesion seen in primary sclerosing cholangitis, but this pattern of ductal injury is not seen in all cases and may be absent in needle biopsy specimens.                                                                                                                                         ';
desc5  = 'Slide 5  </font><br><font id=italictext>Sclerosing Cholangitis Associated with Primary Immunodeficiency</font><br><font id=normaltext>                Sclerosing cholangitis-type changes may be seen in patients with immunodeficiencies, as in this case of common variable immunodeficiency. Such lesions are also seen in patients with AIDS. Various infectious agents such as Cryptosporidium, cytomegalovirus, and microsporidium have been implicated etiologic agents, although none was identified in this case.                                           ';
desc6  = 'Slide 6  </font><br><font id=italictext>Sclerosing Cholangitis Associated with Primary Immunodeficiency</font><br><font id=normaltext>                The interlobular bile duct shows degenerative changes, such as pyknosis, and is surrounded by loose concentric fibrosis.                                                                                                                                                                                                                                                                                       ';
desc7  = 'Slide 7  </font><br><font id=italictext>Adult Idiopathic Ductopenia</font><br><font id=normaltext>                                                    The liver from this 79 year old man shows a biliary pattern of cirrhosis, with "jigsaw puzzle piece" outlines to the regenerating nodules. The extrahepatic and large intrahepatic ducts were normal.                                                                                                                                                                                                          ';
desc8  = 'Slide 8  </font><br><font id=italictext>Loss of Interlobular Bile Ducts in Adult Idiopathic Ductopenia</font><br><font id=normaltext>                 No residual bile duct is identified in many of the portal tracts in this case. Nodular scars suggestive of primary sclerosing cholangitis are not present. Proliferating bile ductules are present at the periphery of the portal tracts, but dilated biliary channels suggestive of a ductal plate malformation are not seen.                                                                                 ';
desc9  = 'Slide 9  </font><br><font id=italictext>Recurrent Pyogenic Cholangitis</font><br><font id=normaltext>                                                 Small portal tracts contain a mixed inflammatory infiltrate with numerous neutrophils. Portal edema and fibrosis may also be seen.                                                                                                                                                                                                                                                                             ';
desc10 = 'Slide 10 </font><br><font id=italictext>Hyperplastic Changes in Bile Duct Epithelium In Recurrent Pyogenic Cholangitis</font><br><font id=normaltext> Ductal epithelium shows crowding and hyperplastic changes without nuclear pleomorphism or hyperchromasia. Cholangiocarcinoma may complicate recurrent pyogenic cholangitis, and is associated with biliary stones.                                                                                                                                                                                             ';
desc11 = 'Slide 11 </font><br><font id=italictext>Acute Rejection in Liver Allograft</font><br><font id=normaltext>                                             A mixed portal inflammatory infiltrate composed of mononuclear cells and scattered eosinophils and neutrophils is present. The interlobular bile ducts are infiltrated by lymphocytes; reactive changes in biliary epithelium such as nuclear enlargement and cytoplasmic vacuolization may also be seen.                                                                                                      ';
desc12 = 'Slide 12 </font><br><font id=italictext>Acute Rejection in Liver Allograft</font><br><font id=normaltext>                                             In endothelialitis, inflammatory cells, predominantly lymphocytes, undermine the endothelium, resulting in detachment of endothelial cells from the underlying connective tissue. Endothelialitis is relatively specific for acute rejection, but is often not present in milder cases of rejection.                                                                                                           ';
desc13 = 'Slide 13 </font><br><font id=italictext>Acute Graft-versus-host Disease</font><br><font id=normaltext>                                                Interlobular bile ducts are the primary target in the liver in acute graft-versus-host disease. A mild lymphocytic infiltrate is often seen around the affected bile ducts, but inflammation is often minimal in relationship to the degree of bile duct injury. The bile duct epithelial cells in this example are sloughed and show degenerative changes. Lymphocytes may also infiltrate biliary epithelium.';
desc14 = 'Slide 14 </font><br><font id=italictext>Loss of Bile Ducts Associated with Drug Therapy and Toxic Epidermal Necrolysis</font><br><font id=normaltext> On low power, minimal portal and lobular inflammation is seen; perivenular and sinusoidal fibrosis is present in zone 3, and scattered canalicular bile plugs are present.                                                                                                                                                                                                                                     ';
desc15 = 'Slide 15 </font><br><font id=italictext>Loss of Bile Ducts Associated with Drug Therapy and Toxic Epidermal Necrolysis</font><br><font id=normaltext> The portal tracts are devoid of bile ducts; no significant inflammatory infiltrate is seen.                                                                                                                                                                                                                                                                                                                    ';
desc16 = 'Slide 16 </font><br><font id=italictext>Bile Duct Injury Associated with Antibiotic Therapy</font><br><font id=normaltext>                            The portal triad contains a mixed inflammatory infiltrate. The interlobular bile duct is almost unrecognizable owing to heavy infiltration of duct epithelium by lymphocytes and neutrophils in this example of drug-induced cholestasis associated with amoxicillin/clavulanate (Augmentin) therapy.                                                                                                          ';
desc17 = 'Slide 17 </font><br><font id=italictext>Congenital Hepatic Fibrosis</font><br><font id=normaltext>                                                    The hepatic parenchyma is distorted by fibrous expansion of portal tracts containing numerous abnormal biliary channels.                                                                                                                                                                                                                                                                                       ';
desc18 = 'Slide 18 </font><br><font id=italictext>Congenital Hepatic Fibrosis</font><br><font id=normaltext>                                                    Dysmorphic anastomosing biliary channels are arranged around the perimeter of the enlarged portal tracts.                                                                                                                                                                                                                                                                                                      ';
desc19 = 'Slide 19 </font><br><font id=italictext>Polycystic Liver Disease</font><br><font id=normaltext>                                                       Multiple unilocular cysts of varying sizes are found in the liver in polycystic liver disease. Biliary hamartomas, or von Meyenburg complexes, are frequently found in the vicinity of the cysts and probably give rise to them by progressive accumulation of fluid.                                                                                                                                          ';
desc20 = 'Slide 20 </font><br><font id=italictext>Polycystic Liver Disease</font><br><font id=normaltext>                                                       The cysts of autosomal dominant polycystic disease involving the liver are lined by a simple cuboidal to low columnar biliary-type epithelium.                                                                                                                                                                                                                                                                 ';
desc21 = 'Slide 21 </font><br><font id=italictext>Caroli\'s Disease</font><br><font id=normaltext>                                                               Involvement of the large intrahepatic bile ducts by the ductal plate malformation process gives rise to congenital dilatation of bile ducts in Caroli\'s disease. These dilated ducts are predisposed to bile stasis, stone formation, and infection.                                                                                                                                                          ';
desc22 = 'Slide 22 </font><br><font id=italictext>Bile Duct Epithelial Hyperplasia in Caroli\'s Disease</font><br><font id=normaltext>                           Biliary epithelial hyperplasia may be seen in ducts involved by Caroli\'s disease. Rarely, frank epithelial dysplasia, which may represent the precursor of cholangiocarcinoma, is seen.                                                                                                                                                                                                                       ';
desc23 = 'Slide 23 </font><br><font id=italictext>Perihilar Cholangiocarcinoma Arising in Primary Sclerosing Cholangitis</font><br><font id=normaltext>         The typical cholangiocarcinoma is well to moderately differentiated, and the tumor cells closely resemble biliary epithelium. A dense desmoplastic stroma usually accompanies the tumor, even in cases not arising in primary sclerosing cholangitis.                                                                                                                                                          ';
desc24 = 'Slide 24 </font><br><font id=italictext>Perineural Invasion in Cholangiocarcinoma</font><br><font id=normaltext>                                      Peri- and intraneural spread is common in cholangiocarcinomas and may serve as a helpful clue to diagnosis of malignancy in small specimens.                                                                                                                                                                                                                                                                   ';
desc25 = 'Slide 25 </font><br><font id=italictext>Adenocarcinoma Arising in Biliary Cystadenoma</font><br><font id=normaltext>                                  Cytologically malignant cells forming cribriform and papillary structures infiltrate the cyst wall.                                                                                                                                                                                                                                                                                                            ';
desc26 = 'Slide 26 </font><br><font id=italictext>Biliary Cystadenoma with Mesenchymal Stroma</font><br><font id=normaltext>                                    The cysts of biliary cystadenoma are lined by simple columnar to cuboidal epithelium; goblet cells are occasionally seen. The underlying mesenchymal stroma may be densely packed and resemble ovarian stroma, a feature found exclusively in female patients.                                                                                                                                                 ';

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