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1.
J Trop Pediatr ; 66(4): 448-457, 2020 08 01.
Artigo em Inglês | MEDLINE | ID: mdl-31943108

RESUMO

OBJECTIVES: To describe the clinical characteristics, biochemical and histological features, outcomes and predictors of prognosis of children with autoimmune hepatitis (AIH) from a paediatric centre in South Africa. METHODS: Thirty-nine children diagnosed with AIH at Red Cross War Memorial Children's Hospital between 2005 and 2015 were included. Relevant patient's data were retrieved from the hospital's medical records and database. Liver biopsy slides were reviewed. Ethical approval was obtained. Data were analysed using SPSS. RESULTS: Females were 29 (74%). Mean age at presentation was 7.27 ± 3.35 years and the mean follow-up was 4.5 ± 2.4 years. Jaundice was present in 97% of patients at presentation. An acute presentation was observed in 26 (67%) even though cirrhosis was detected in 22 (56%). Autoantibody screening was completed in 35 patients, 20 (57%) were AIH-1, 1 (3%) was AIH-2 and 14 (40%) were seronegative AIH. Of the 25 patients who underwent magnetic resonance cholangiography 17 (68%) had associated autoimmune sclerosing cholangitis. The remission rate was 79%. However, 11 children relapsed later. One child required liver transplantation and one demised. Seronegative and seropositive patients have comparable characteristics and outcomes. While a higher alanine transaminase (ALT) level at presentation is a significant predictor of remission, a lower ALT level and cirrhosis are significant risk factors for unfavourable outcome. Overall survival rate was 97%. CONCLUSION: AIH responds well to therapy with excellent survival. Hence, it should be considered in any child presenting with viral screen negative hepatitis and start therapy timeously to prevent disease progression.


Assuntos
Colangiopancreatografia por Ressonância Magnética/métodos , Colangite Esclerosante/diagnóstico por imagem , Hepatite Autoimune/diagnóstico , Imunossupressores/uso terapêutico , Autoanticorpos/imunologia , Autoanticorpos/uso terapêutico , Azatioprina/uso terapêutico , Biópsia , Criança , Pré-Escolar , Colangite Esclerosante/tratamento farmacológico , Colangite Esclerosante/imunologia , Feminino , Glucocorticoides/uso terapêutico , Hepatite Autoimune/tratamento farmacológico , Hepatite Autoimune/imunologia , Humanos , Fígado/patologia , Masculino , Prednisolona/uso terapêutico , África do Sul , Resultado do Tratamento
2.
J Trop Pediatr ; 65(3): 305-308, 2019 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-30085268

RESUMO

Collagenous gastritis is an uncommon gastrointestinal disease in children. Its cause remains uncertain. It may present as severe hypoproteinaemia manifesting as generalized oedema. We report a 15 months old female who presented with pica, generalized body oedema and diarrhoea. Diagnostic workup revealed gastric replacement of the lamina propria by hyalinized collagen on histology. This case seeks to highlight the need for early paediatric gastroenterology referral including oesophagogastroduodenoscopy with multiple tissue biopsies as part of a broad diagnostic workup in children with non-specific gastrointestinal symptoms to improve diagnostic yield and enable accurate histologic diagnosis, so that appropriate therapy can be timeously applied.


Assuntos
Anemia Ferropriva/etiologia , Colágeno/análise , Diarreia/etiologia , Edema/etiologia , Albuminas/administração & dosagem , Azatioprina/administração & dosagem , Biópsia , Endoscopia Gastrointestinal , Feminino , Mucosa Gástrica/patologia , Gastrite/complicações , Gastrite/tratamento farmacológico , Gastrite/patologia , Humanos , Hipoalbuminemia/diagnóstico , Hipoalbuminemia/tratamento farmacológico , Hipoproteinemia/diagnóstico , Hipoproteinemia/tratamento farmacológico , Lactente , Pica/etiologia , Prednisona/administração & dosagem , Resultado do Tratamento , Equilíbrio Hidroeletrolítico
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