Ipertransaminasemia

Sclerosi epatoportale

Sparaventi C, Zago A, Di Leo G, Barbi E, Bramuzzo M.

2025/7 — pag. 453-455 — DOI

Hepatoportal sclerosis is a rare and underdiagnosed liver condition characterised by histological alterations of the portal venules and hepatic sinusoids, with periportal fibrosis and vascular narrowing. Its diagnosis is histological and requires liv...

Colecistite acuta da EBV

Favaretto E

2025/1 — pag. 21-22 — DOI

The paper describes a rare instance of acute acalculous cholecystitis (ACC) in a 7-year-old boy caused by Epstein-Barr virus (EBV) infection. Initially, he was suspected to have appendicitis, but subsequently imaging and laboratory tests revealed ACC...

Ipotonia e ipertransaminasemia: pensa alla fruttosemia

Zanetto L, Benelli E.

2022/9 — pag. 598-600 — DOI

The case of a 3-month-old acutely hypotonic and hyporeactive girl is described. The diagnosis of fructosemia was eventually posed. The clinical, diagnostic and therapeutic implications of fructosemia are also discussed....

Sclerosi epatoportale

Di Stasio F, Amoroso A, Melzi ML.

2022/2 — pag. 124-126 — DOI

Hepatoportal sclerosis (HS) is a syndrome of obscure aetiology that may evolve in noncirrhotic portal hypertension. The paper reports the case of a 3-month-old infant presenting with HS and isolated liver enzymes elevation....

Un’inaspettata convulsione… epatica

B. Cristiani, M. Di Pietro, G. Tezza, H. Egger

2019/9 — pag. 233-233

Le molte facce della istiocitosi a cellule di Langerhans

L. Picciano, R. Mancusi, M.C. Fedele, F. Palladino

2019/3 — pag. 52-52

Ipertransaminasemia ed epatomegalia: cerca una diagnosi!

C. Di Chiara, G. D’Onofrio, P.M. Pavanello, S. Martelossi

2019/2 — pag. 34-34

È il Turner delle transaminasi

M. Mainetti, L. Mambelli, M. Cozzolino, F. Marchetti

2019/1 — pag. 47-48

Un caso di ipertransaminasemia più unico che raro

G. Maggiore, G. Rossi, S. Baldini

2015/9

Malattia di Wilson: dieci motivi per (ri)parlarne ai pediatri

R. Iorio, G. Ranucci, D. Liccardo, M.G. Puoti, F. Di Dato

2012/8 — pag. 501-507

Wilson disease (WD) is an inherited autosomal recessive disorder of copper metabolism characterized by progressive copper accumulation in the liver and then in other organs, such as the nervous system, eyes and kidneys. In childhood, clinical prese...

Fegato grosso e grasso: poche diagnosi a cui pensare

M. Mainetti, M. Grassi, A. Zucchini, L. Mambelli, F. Dal Monte, D. Cassandrini, G. Maggiore, F. Marchetti

2012/8

The case of an 8-year-old girl with an isolated hypertransaminasemia asymptomatic without cholestasis and with moderate hypercholesterolemia and hepatomegaly with steatosis and glycogen storage in biopsy is described. Once excluded the commonest ...

Una doppia colestasi in famiglia

G. Paloni, C. Zanchi, D. Giglia, F. Mastrobuoni

2008/7

Un’ipertransaminasemia urso-dipendente

G. Ranucci, F. Cirillo, L. D’Antiga, M. Tufano, M. D’Ambrosi,G. Giordano, R. Iorio

2008/3 — pag. 193-194

We present a case of a 6 year-old boy with chronic hypertransaminasemia referred to our observation at the age of 17 months, with ALT levels of 2,147 IU/L without signs of cholestasis. Main causes of hypertransaminasemia were excluded and liver b...

Un'ipertransaminasemia urso-dipendente

Giusy Ranucci, Francesco Cirillo, Lorenzo D’Antiga, Maria Tufano, Mariangela D’Ambrosi, Giuseppe Giordano, Raffaele Iorio

2008/3

Un caso di sindrome di Alagille

A. Borrelli, M. Teresa Carbone, A. Correra

2005/6

Un caso di ipertransaminasemia

M. Lazzerini

2003/8

Un caso di ipertransaminasemia

M. Lazzerini

2003/8

Un caso di ipertransaminasemia

M. Lazzerini

2003/8

Un caso di ipertransaminasemia

M. Lazzerini

2003/8