cholestasis

Parvovirus: un solo virus per tante malattie

Burlo F, Colussi L, Zanchi C, Bloise S, Marchetti F, Cozzi G.

2025/4 — pag. 229-234 — DOI

Parvovirus B19 causes a wide range of clinical manifestations, with a peak incidence between 5 and 15 years of age. The spectrum of clinical manifestations associated with Parvovirus infection varies depending on the host's age, haematological status...

Rivista sfogliabile on line

2024/6

Colestasi neonatale e fibrosi cistica

Maggiore G.

2024/6 — pag. 116-117 — DOI

The diagnosis of cystic fibrosis was eventually made in a one-month-old infant with cholestasis. The newborn screening for cystic fibrosis had been falsely negative....

Le colelitiasi a origine ematologica

Fantasia M, Faraguna MC, Ferrari GM, Corti P.

2024/3 — pag. 187 — DOI

A 7-year-old girl presenting with acute abdominal pain due to gallstones was eventually diagnosed with spherocytosis....

Un’insolita ipertensione polmonare

Todero S, Hasan T, Ragni L, Donti A

2023/1 — pag. 13-13 — DOI

The Authors describe the case of a newborn presenting with severe pulmonary hypertension due to the hypoplasia of the pulmonary arteries and finally diagnosed with Alagille syndrome. The typical vertebral anomalies and hyperbilirubinaemia were also p...

Secondo i miei “calcoli”... non è una gastrite

Arnaboldi S, Quattrocchi G, Ferrari GM, Corti P

2022/6 — pag. 129-130 — DOI

The case of an 11-year-old girl affected by hereditary spherocytosis admitted to hospital for abdominal pain is described. The diagnosis of cholelithiasis was eventually made....

Diagnosi delle colestasi neonatali e infantili

Maggiore G, Della Corte C.

2022/4 — pag. 244-248 — DOI

Neonatal and infantile cholestasis (NIC) may represent the onset of a surgically correctable disease and of a genetic or metabolic disorder worthy of medical treatment. Timely recognition of NIC and identification of the underlying aetiology are para...

Che faccia di bronzo! L’atresia delle vie biliari

Morra L, Risso FM, Travan L

2022/4 — pag. 94-94 — DOI

The case of a newborn treated for haemolytic anaemia and hyperbilirubinaemia is described. An Extrahepatic Biliary Atresia (EBA) was eventually suspected after the appearance of a bronze discoloration of the skin....

Gialla fuori... e gialla dentro

A.G. Grasso

2020/9 — pag. 236-236 — DOI

Un ittero neonatale colestatico: semaforo verde!

F.M. Risso

2020/7 — pag. 461-463 — DOI

Un prolasso nell’ambulatorio... “sbagliato”

A. Daidone

2020/7 — pag. 461-463 — DOI

Un ittero colestatico neonatale: la sindrome di Alagille

E. Rizzello, J. Bua, S. Nider

2019/9 — pag. 226-227

Il neonato a colori: le sfumature di grigio

G. Corsello, M. Schierz

2019/7 — pag. 455-456

Lattanti e trapianti

F. Fusco

2018/10 — pag. 662-663

Una ragazza con ascite e diarrea con sangue: quale diagnosi?

F. Marchetti, M. Mainetti, M. Giovannini, C. Morelli

2017/8 — pag. 519-522

Kawasaki facile e difficile

E. Benelli, S. Carbogno, N.S. Carucci, M. Gori, E. Marrani, M. Melis, M.C. Pellegrin

2017/3 — pag. 155-162

Kawasaki disease (KD) is a systemic vasculitis that typically affects children of 2-5 years of age and whose diagnosis and treatment are usually easy, as described in the first case report. Anyway, in spite of adequate therapy, 10-15% of patients d...

MAS in WAS? (una Wiskott-Aldrich non convenzionale)

S. Amoroso

2016/10

Profilassi del sanguinamento da deficit di vitamina K: finalmente la luce?

G. Maggiore, S. Demarini

2016/8 — pag. 483-485

Nuove evidenze sulla profilassi neonatale con vitamina K

C. Lama, S. Pusceddu, P. Gallo, F. Marchetti

2016/8 — pag. 531-533

Nuove evidenze sulla profilassi neonatale con vitamina K

C. Lama, S. Pusceddu, P. Gallo, F. Marchetti

2016/8

Epatite acuta con colestasi da Parvovirus B19

S. Perrini, b. Guidi, P. Torelli, A. Forte

2015/2 — pag. 119-121

Few cases of acute hepatitis due to Parvovirus B19 are reported in the literature. The paper describes a case of acute cholestatic hepatitis due to Parvovirus B19 infection. Diagnosis was based on a positive serologic test (IgM) and on molecular dete...

Epatite acuta con colestasi da Parvovirus B19

S. Perrini, B. Guidi, P. Torelli, A. Forte

2015/2

Few cases of acute hepatitis due to Parvovirus B19 are reported in the literature. The paper describes a case of acute cholestatic hepatitis due to Parvovirus B19 infection. Diagnosis was based on a positive serologic test (IgM) and on molecular dete...

Quando lo striscio è patognomonico

Anna Delise, Martina Tubaro

2014/6

Una colestasi senza prurito

L. Matarazzo, S. Martelossi, G. Maggiore, G.P. Chiaffoni , A. Ventura

2013/5

Bile acids deficiency is characterized by an inadequate synthesis of bile salts with accumulation of abnormal hepatotoxic metabolites and liver damage. High levels of abnormal bile acid are found in urine. Clinical features include jaundice without i...

Un caso di febbre persistente

R. Puxeddu, A.P. Pinna, V. Pisano, A. Doneddu, S. Marras, A.M. Nurchi

2012/8

Ittero in un lattante: quando l’assassino è proprio il maggiordomo

M. Bensa, E. Gubellini, M. Bramuzzo

2010/8 — pag. 525-526

L’esplorazione bioumorale del fegato: il bilancio epatico

G. Maggiore

2009/10 — pag. 649-653

Liver function tests are a simple way to explore liver function and are a helpful tool to the clinician to confirm the clinical suspect of liver disease. Practically, evaluation of liver function includes determination of total and conjugated bilir...

Atresia delle vie biliari: quali insidie per il pediatra?

R. Iorio, A.M. Salzano, F. Cirillo, G. Vallone

2009/4 — pag. 224-231

Biliary atresia (BA) is the most common pediatric cause of cirrhosis, end-stage liver disease and indication for liver transplantation. The clinical presentation is characterized by jaundice with yellow or dark urine and pale stools, which eventually...

Colestasi neonatale: la grande simulatrice

M. Tufano, F. Cirillo, G. Ranucci, R. Vecchione, A. Sonzogni, D. Alberti, R. Iorio

2008/8 — pag. 527-529

Early detection and accurate diagnosis of cholestatic jaundice (CJ) are important for successful treatment and favourable prognosis but the rapid and effective recognition of the causes of cholestasis in infants is still challenging also for paed...

Colestasi neonatale: la grande simulatrice

M. Tufano, F. Cirillo, G. Ranucci, R. Vecchione, A. Sonzogni, D. Alberti, R. Iorio

2008/8

Una doppia colestasi in famiglia

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

2008/7

Atresia biliare: non è mai troppo prestoStipsi severa nei bambini: non serve lo psicologoEstremi mali, estremi rimedi: chirurgia bariatrica per l'obesità grave dei bambini?Vaccino anti-Rotavirus umano attenuato: efficace anche "al di là dal mare"Neonati e “lattantini”: meglio distesi che seduti

2008/5 — pag. 283-284

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...

La storia vera, ma troppo lunga, di un lattante con ittero

V. Rametta, L. Zancan

2006/6 — pag. 385-386

Una disfagia per i cibi solidi in un ragazzo di 12 anni

L. Travan, P. Salierno, S. Martelossi

2005/7

Un caso di sindrome di Alagille

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

2005/6

Un caso di sindrome di Alagille

A. Borrelli, Mt. Carbone, A. Correra

2005/6 — pag. 398-398

Il deficit di alfa1-antitripsina in età pediatrica

L. Giglio, I. Berti, C. Trevisiol

2003/3 — pag. 155-161

Alpha 1-antitrypsin deficiency (AATD) is an autosomal recessive disease, with more than 70 genetic variants, and a frequency which varies from 1:1000 to 1:5000, depending on genetic epidemiology and screening methods. The AATD involves primarily th...

Ittero tardivo e atresia delle vie biliariTra il dire e il fare: ITra il dire e il fare: IIRisposte fisiologiche a fisiologici bisogni

2003/3 — pag. 149-151

Il trattamento del prurito

G. Bartolozzi

2003/2

Colestasi nella mononucleosi infettiva da virus di Epstein-Barr

F. Massei, G. Palla, C. Ughi, et al.

2002/5 — pag. 308-310

Although biochemical evidence of liver damage is frequent in children with EBV infectious mononucleosis, signs or symptoms related to an impaired bile flow as jaundice or pruritus are rare. The Authors report three cases observed in a two-year peri...

Ittero colestatico in un bambino di un meseUn caso clinico personale di 10 anni fa

G. Bartolozzi

2002/3

La diagnosi di ittero colestatico nel neonato

G. Maggiore, S. Caprai

1999/3 — pag. 157-161

The incidence of cholestatic jaundice in newborn babies is 1/2500 live births. Biliary atresia is the most frequent single cause of neonatal cholestasis, its frequency is 1/10.000 live births. The prognosis is strictly related to early surgical tre...

Fegato a ultrasuoni

G. Maggiore, M. Massimetti

1998/1 — pag. 17-22

Over the past two decades ultrasonography (US) have emerged as the principal imaging method for diagnostic examination of the liver and biliary tree. US is relatively not expensive and safe: the single major disadvantage is its dependence upon a...