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7. Congenital hepatic fibrosis: Difference between revisions
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(Created page with "'''Staining''': HE '''Organ''': Liver '''Description''': In the slide we can se normal parenchyme. In the background we can se a hypercellular eosinophilic area containing fibrosis and abnormal bile ducts. '''Diagnosis''': Congenital liver fibrosis '''Theory''': Fibropolycystic liver disease is a collective term for a group of congenital liver and biliary abnormalities resulting from abnormal development of the ductal plates. Diseases in this group include: * Cong...") |
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'''Staining''': HE | [[File:Congenital hepatic fibrosis - overview.png|thumb|Overview|438x438px]]'''Staining''': HE | ||
'''Organ''': Liver | '''Organ''': Liver | ||
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In the background we can se a hypercellular eosinophilic area containing fibrosis and abnormal bile ducts. | In the background we can se a hypercellular eosinophilic area containing fibrosis and abnormal bile ducts. | ||
'''Diagnosis''': Congenital liver fibrosis | '''Diagnosis''': Congenital liver fibrosis[[File:Congenital hepatic fibrosis - fibrosis.png|thumb|Hypercellular eosinophilic area showing fibrosis and abnormal bile ducts|443x443px]]'''Theory''': Fibropolycystic liver disease is a collective term for a group of congenital liver and biliary abnormalities resulting from abnormal development of the ductal plates. Diseases in this group include: | ||
'''Theory''': Fibropolycystic liver disease is a collective term for a group of congenital liver and biliary abnormalities resulting from abnormal development of the ductal plates. Diseases in this group include: | |||
* Congenital liver fibrosis (recessive polycystic liver disease) | * Congenital liver fibrosis (recessive polycystic liver disease) | ||
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''Written by G cobra'' | ''Written by G cobra'' | ||
[[Category:Pathology 2 - Histopathology slides]] | [[Category:Pathology 2 - Histopathology slides]] | ||