Autor: |
Vicent, Martínez I Cózar, Margarita, Llavador Ros, Montserrat, Évole Buselli, María Del Mar, Andrés Moreno, Begoña, Polo Miquel, Judith, Pérez Rojas |
Rok vydání: |
2018 |
Předmět: |
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Zdroj: |
Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia. 55(1) |
ISSN: |
1988-561X |
Popis: |
Neonatal cholestasis is a clinical metabolic alteration requiring investigation of its eitiology. It is characterized by elevation of liver enzymes with cholestasis pattern and, in some cases, with acute liver failure. Its etiology is variable although the most frequent cause is atresia of extrahepatic bile ducts. We present a case of a 23-month-old boy who presented with cholestasis and was finally diagnosed with systemic Langerhans cell histiocytosis. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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