Case Report

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.

An Under Recognized Entity That Need Awareness Hyper Elasticity and Associated Diseases Especially Superior Mesenteric Artery Syndrome

Dear Editors During our practice in UAE, we came across many rare and unusual disease presentations that were missed by many centers because of either: Lack of awareness or failure to check detailed history including family history and proper physical examination. Joint hypermobility alone is common in the general population, affecting approximately 10 to 20 …

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