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1.
Clinics ; 73: e289, 2018. tab, graf
Article in English | LILACS | ID: biblio-952809

ABSTRACT

OBJECTIVE: The prognosis of patients with biliary atresia undergoing Kasai portoenterostomy is related to the timing of the diagnosis and the indication for the procedure. The purpose of the present study is to present a practical flowchart based on 257 children who underwent Kasai portoenterostomy. METHODS: We conducted a retrospective cohort study of patients who underwent Kasai portoenterostomy between 1981 and 2016. RESULTS: During the first period (1981 to 2009), 230 infants were treated, and the median age at the time of surgery was 84 days; jaundice was resolved in 77 patients (33.5%). During the second period, from 2010 to 2016, a new diagnostic approach was adopted to shorten the wait time for portoenterostomy; an ultrasonography examination suggestive of the disease was followed by primary surgical exploration of the biliary tract without complementary examination or liver biopsy. Once the diagnosis of biliary atresia was confirmed, a portoenterostomy was performed during the same surgery. During this period, 27 infants underwent operations; the median age at the time of surgery was 66 days (p<0.001), and jaundice was resolved in 15 patients (55.6% - p=0.021), with a survival rate of the native liver of 66.7%. CONCLUSION: Primary surgical exploration of the biliary tract without previous biopsy was effective at improving the prognostic indicators of patients with biliary atresia undergoing Kasai portoenterostomy.


Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Biliary Atresia/surgery , Portoenterostomy, Hepatic/methods , Time Factors , Biliary Atresia/mortality , Biliary Atresia/pathology , Brazil/epidemiology , Portoenterostomy, Hepatic/mortality , Survival Rate , Retrospective Studies , Age Factors , Liver Transplantation/methods , Liver Transplantation/mortality , Treatment Outcome , Kaplan-Meier Estimate , Jaundice, Neonatal/surgery , Jaundice, Neonatal/pathology , Liver/surgery , Liver/pathology
2.
Clinics ; 63(5): 689-694, 2008. graf
Article in English | LILACS | ID: lil-495046

ABSTRACT

BACKGROUND AND AIMS: Although there is much known about liver diseases, some aspects remain unclear, such as the nature of the differences between the diseases observed in newborn infants and those in adults. For example, how do newborns respond to duct epithelial cell injury? Do the stellate cells in newborns respond similarly to those in adults during biliary obstruction? METHODS: Ninety newborn Wistar rats aged six days, weighing 8.0 - 13.9 g each, and 90 adult rats weighing 199.7 - 357.0 g each, were submitted to bile duct ligation. After surgery, they were randomly divided and sacrificed on the 3rd, 5th, 7th, 14th, 21st or 28th day post-bile duct ligation. Hepatic biopsies were obtained and immunohistochemical semi-quantification of desmin and á-SMA expression was performed in hepatic stellate cells and in myofibroblasts in the portal space, and between the portal space and the liver lobule. RESULTS: Desmin expression in the myofibroblast cells post-bile duct ligation was higher in young rats, reaching its peak level in a shorter time when compared to the adult animals. The differences between the groups for á-SMA expression were less significant than for desmin. CONCLUSIONS: These findings indicate that there is an increase in the number of collagen-producing myofibroblast cells in young animals, suggesting that there is more intense fibrosis in this population. This finding may explain why young animals with bile duct obstruction experience more intense portal fibrosis that is similar to the pathology observed in the livers of newborns with biliary atresia.


Subject(s)
Animals , Female , Male , Rats , Biliary Atresia/pathology , Cholestasis/pathology , Fibroblasts/pathology , Hepatic Stellate Cells/pathology , Portal System/pathology , Age Factors , Animals, Newborn , Actins/analysis , Biomarkers/analysis , Disease Models, Animal , Desmin/analysis , Extracellular Matrix Proteins/analysis , Ligation , Rats, Wistar
3.
São Paulo; s.n; 2003. [83]] p. ilus, tab, graf.
Thesis in Portuguese | LILACS | ID: lil-405097

ABSTRACT

A atresia das vias biliares é afecção hepática da infância. A etiologia é desconhecida, e o diagnóstico baseia-se na biópsia hepática, cujo achado é a proliferação ductular. A ligadura do ducto biliar comum em ratos é modelo utilizado para estudo das doenças colestáticas. A proposta do trabalho foi estudar, em modelo experimental de obstrução biliar, as alterações histológicas hepáticas em ratos jovens e compará-las com o animal adulto / Biliary atresia is an hepatic disease of infancy. Etiology is unknown, and diagnosis is made by liver biopsy, with ductular proliferation being the main histological feature. Bile duct ligation in rats is an useful experimental model of biliary obstruction. The aim of this study of extra-hepatic cholestasis was analyse hepatic histological alterations in young rats compared to adult animals...


Subject(s)
Animals , Male , Female , Rats , Biliary Atresia , Cholestasis, Extrahepatic/pathology , Disease Models, Animal , Fibrosis/pathology , Histology, Comparative , Immunohistochemistry , Rats, Wistar
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