Literature DB >> 28685316

[Liver biopsy in children and adolescents : Preliminary morphological examinations in diffuse liver disease].

C Lackner1, A S Knisely2.   

Abstract

BACKGROUND: Frequencies of types of liver disease differ between adults and nonadults (NA).
OBJECTIVES: The particular problems encountered in interpreting liver-biopsy findings in NA often require referral in consultation.  To permit this efficiently, we recommend specific approaches to light microscopy, with special stains and immunohistochemistry, as well as to ultrastructural study.
METHODS: Prosection and the choice of special stains are described, and are discussed in relation to clinical questions.
RESULTS: Histochemical stains (chromatic aniline blue [CAB], Prussian blue [Berlin blue, BBL], periodic acid-Schiff reaction [PAS], diastase-PAS [D‑PAS], reticulin, rhodanine, Victoria blue) and immunohistochemical studies to demonstrate the expression of keratin 7 (cholangiocytes) and macrosialin (CD68; macrophages) as well as electron microscopy are important techniques in the histopathologic  analysis of ontogenetic, storage, and metabolic disorders, hepatitis, hepatosplenomegaly, cholestasis, and portal hypertension.
CONCLUSIONS: Particular histochemical and immunohistochemical studies, as well as electron microscopy, are useful in optimising histopathologic diagnosis and in differential diagnosis.  We believe that these techniques should be part of routine work-up of NA liver-biopsy specimens.

Entities:  

Keywords:  Consultation; Electron microscopy; Histochemical stains; Histopathology; Immunohistochemistry; Pediatric liver diseases

Mesh:

Year:  2017        PMID: 28685316     DOI: 10.1007/s00292-017-0306-9

Source DB:  PubMed          Journal:  Pathologe        ISSN: 0172-8113            Impact factor:   1.011


  3 in total

1.  Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's disease.

Authors:  M Anheim; P Chamouard; G Rudolf; B Ellero; L Vercueil; B Goichot; C Marescaux; C Tranchant
Journal:  Clin Genet       Date:  2010-09       Impact factor: 4.438

2.  Presentation of Progressive Familial Intrahepatic Cholestasis Type 3 Mimicking Wilson Disease: Molecular Genetic Diagnosis and Response to Treatment.

Authors:  Salih Boga; Dhanpat Jain; Michael L Schilsky
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2015-09-25

3.  Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis.

Authors:  Natalia Gomez-Ospina; Carol J Potter; Rui Xiao; Kandamurugu Manickam; Mi-Sun Kim; Kang Ho Kim; Benjamin L Shneider; Jennifer L Picarsic; Theodora A Jacobson; Jing Zhang; Weimin He; Pengfei Liu; A S Knisely; Milton J Finegold; Donna M Muzny; Eric Boerwinkle; James R Lupski; Sharon E Plon; Richard A Gibbs; Christine M Eng; Yaping Yang; Gabriel C Washington; Matthew H Porteus; William E Berquist; Neeraja Kambham; Ravinder J Singh; Fan Xia; Gregory M Enns; David D Moore
Journal:  Nat Commun       Date:  2016-02-18       Impact factor: 14.919

  3 in total

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