Liver transplantation for children with acute liver failure associated with secondary hemophagocytic lymphohistiocytosis
Achiya Z. Amir, Simon C. Ling, Ahmed Naqvi, Sheila Weitzman, Annie Fecteau, David Grant, Anand Ghanekar, Mark Cattral, Nadya Nalli, Ernest Cutz, Binita Kamath, Nicola Jones, Maria Angelis, Vicky Ng, Yaron Avitzur – 23 May 2016 – Hemophagocytic lymphohistiocytosis (HLH) is a rare life‐threatening systemic disease, characterized by overwhelming stimulation of the immune system and categorized as primary or secondary types. Occasionally, acute liver failure (ALF) may dominate the clinical presentation.