Analysis of the histologic features in the differential diagnosis of intrahepatic neonatal cholestasis

AIM: To compare the histologic features of the liver in intrahepatic neonatal cholestasis (IHNC) with infectious, genetic-endocrine-metabolic, and idiopathic etiologies. METHODS: Liver biopsies from 86 infants with IHNC were evaluated. The inclusion criteria consisted of jaundice beginning at 3 mo o...

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Published inWorld journal of gastroenterology : WJG Vol. 15; no. 4; pp. 478 - 483
Main Authors Bellomo-Brandao, Maria Angela, Escanhoela, Cecilia A F, Meirelles, Luciana R, Porta, Gilda, Hessel, Gabriel
Format Journal Article
LanguageEnglish
Published United States Department of Pediatrics, Faculty of Medical Sciences, State University of Campinas (UNICAMP), Campinas-SP 13083-970, Brazil%Department of Pathology, Faculty of Medical Sciences, State University of Campinas (UNICAMP), Campinas-SP 13083-970, Brazil%Department of Pediatrics, Children's Institute of Medical School of the University of S(a)o Paulo (USP), S(a)o Paulo-SP 05403-000, Brazil 28.01.2009
The WJG Press and Baishideng
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Summary:AIM: To compare the histologic features of the liver in intrahepatic neonatal cholestasis (IHNC) with infectious, genetic-endocrine-metabolic, and idiopathic etiologies. METHODS: Liver biopsies from 86 infants with IHNC were evaluated. The inclusion criteria consisted of jaundice beginning at 3 mo of age and a hepatic biop- sy during the 1st year of life. The following histologic features were evaluated: cholestasis, eosinophilia, giant cells, erythropoiesis, siderosis, portal fibrosis, and the presence of a septum. RESULTS: Based on the diagnosis, patients were classified into three groups: group 1 (infectious; n = 18), group 2 (genetic-endocrine-metabolic; n = 18), and group 3 (idiopathic; n = 50). There were no significant differences with respect to the following variables: cholestasis, eosinophilia, giant cells, siderosis, portal fibrosis, and presence of a septum. A significant dif- ference was observed with respect to erythropoiesis, which was more severe in group 1 (Fisher's exact test, P = 0.016). CONCLUSION: A significant difference was observed in IHNC of infectious etiology, in which erythropoiesis was more severe than that in genetic-endocrine-meta- bolic and idiopathic etiologies, whereas there were no significant differences among cholestasis, eosinophilia, giant cells, siderosis, portal fibrosis, and the presence of a septum.
Bibliography:Intrahepatic cholestasis; Liver histopathol-ogy; Neonatal jaundice; Neonatal liver disease
Neonatal jaundice
14-1219/R
R575.63
Neonatal liver disease
Liver histopathol-ogy
Intrahepatic cholestasis
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Fax: +55-19-35217193
Author contributions: Bellomo-Brandao MA had responsibility for protocol development, collection of patients’ data, preliminary data analysis and writing the manuscript; Escanhoela CAF was responsible for histological analysis and helped to draft the manuscript; Meirelles LR was responsible for histological analysis; Porta G participated in the development of the protocol; Hessel G conceived of the study, and participated in its design and helped to draft the manuscript; All authors read and approved the final manuscript.
Telephone: +55-19-35792998
Correspondence to: Maria Angela Bellomo-Brandao, Department of Pediatrics, Faculty of Medical Sciences, State University of Campinas (UNICAMP), Rua Aristides Lobo, 789. Campinas, São Paulo 13083-060, Brazil. bellomobrandao@globo.com
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.15.478