7. Congenital hepatic fibrosis: Difference between revisions
(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]] | ||
Latest revision as of 13:25, 7 July 2024
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:
- Congenital liver fibrosis (recessive polycystic liver disease)
- Caroli syndrome
- Von Meyenburg complex
- dominant polycystic liver disease
DD between Caroli syndrome and congenital liver fibrosis is done by the presence of bile in the abnormal bile ducts and cholestasis, which can be seen in the former. Congenital liver fibrosis is accociated with polycystic kidney disease.
Written by G cobra