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Mastocytosis overview including pathogenesis, clinical features, diagnosis, and management with mnemonics for medical students and nursing students. Discussion of Stem Cell Factor, KIT, and Darier’s Sign. and other extra-articular features associated with the condition and Crohn’s disease or Ulcerative colitis. Novel memory tricks at the end! With a breakdown of the classification of mastocytosis - Cutaneous mastocytosis is commonly diagnosed in young children and disease is limited to the skin with an absence of pathologic infiltrates in internal organs. There are 3 variants of the cutaneous disease: 1. Maculopapular cutaneous mastocytosis 2. Diffuse cutaneous mastocytosis 3. Solitary mastocytoma Systemic forms of the disease mostly affect adults and can infiltrate organs. There are 5 variants of this version which can be indolent or aggressive: 1. Indolent systemic mastocytosis (ISM) 2. Smoldering systemic mastocytosis 3. Systemic mastocytosis with an associated clonal hematologic non–mast cell lineage disease (SM-AHNMD) 4. Aggressive systemic mastocytosis (ASM) 5. Mast cell leukemia (MCL) 0:00 Introduction 0:21 Physiology 0:52 Pathogenesis 1:30 Classification 2:08 Clinical Features 3:53 Investigations 4:32 Management 5:14 Mnemonic Disclaimer: This video was intended for educational purposes only and not to be considered medical advice. All information was sourced from a combination of reputable sources including BMJ Best Practice, ETG (Australia), UpToDate, and Harrison’s Principles of Internal Medicine. #medicalmnemonics #medicalstudents #nursingstudents #highyield