An Uncommon Manifestation of Secondary Hemophagocytic Lymphohistiocytosis (HLH) Precipitated by Candida Auris – A Case Report
Hemophagocytic Lymphohistiocytosis (HLH) is a rare but severe sys temic inflammatory syndrome, often classified under autoimmune conditions. It is characterised by the excessive activation and proliferation of cytotoxic T cells and histiocytes (macrophages), leading to widespread immune dysregulation. There are two types of HLH one is primary and the other is secondary.