focal nodular hyperplasia of the liver, hepatic focal nodular hyperplasia, FNH (previous denomination: benign hepatoma, solitary hyperplastic nodule, focal sclerosis, hamartomatous cholangiohepatoma, mixed adenoma)
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Microscopy
See also the Pathology Digital Slidebox.
Articles
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focal nodular hyperplasia
29 May 2003 -
actinic keratosis
6 July 2004solar keratosis, senile keratosis, pre-epitheliomatous keratosis WKP
Digital cases
UI:906 - Actinic keratosis.
UI:917 - Actinic keratosis.
UI:1826- Actinic keratosis.
JRC:10567 : Actinic keratosis.
JRC:10569 : Actinic keratosis.
Definition: Actinic keratosis is a premalignant condition of thick, scaly, or crusty patches of skin
It is more common in fair-skinned people and it is associated with those who are frequently exposed to the sun, as it is usually accompanied by (...) -
hepatoblastoma
16 March 2004hepatoblastomas
Definition: Hepatoblastoma is a malignant embryonal liver tumor that occurs almost exclusively in infants and very young children.
Image
Macroscopy : https://twitter.com/DraEosina/status/762631086207893506
Cytology: https://twitter.com/AdamGomezMD/status/720632495671087104
https://twitter.com/MArnold_PedPath/status/736000944303808512
Hepatoblastoma is composed of epithelial and mesenchymal elements in varying proportions and at various stages of differentiation. The (...) -
neonatal enteropathies
10 August 2004intractable diarrhoea, protracted diarrhea of infancy, intractable diarrhea
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Wilms tumor
14 November 2003nephroblastoma
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familial adenomatous polyposis
20 November 2003adenomatous polyposis, FAP
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hepatic hematopoiesis
4 June 2003hepatic extramedullary hematopoiesis, hepatic myeloid ’metaplasia’
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monosomy X
25 January 2005Turner syndrome, constitutional monosomy X, Turner-Albright syndrome, Ullrich-Turner syndrome
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ductular reaction
25 June 2003neoductular proliferation, portal ductal proliferation, ductular proliferation
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North American Indian childhood cirrhosis
9 October 2008North American Indian childhood cirrhosis (NAIC) have been described an isolated nonsyndromic form of cholestasis in Ojibway-Cree children from First Nations communities in the Abitibi region of northwestern Quebec, Canada.
The disease typically presents, in a child who is otherwise well, with transient neonatal jaundice that progresses to biliary cirrhosis requiring hepatic transplantation in childhood or early adulthood.
The biochemical and histopathologic features of the disease (...)