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rheumatology cardiology disease hemophagocytic hlh lymphohistiocytosis algorithm arthritis behcet cor cortriatriatum cryptogenic dermatology fallot gravis hemeonc incomplete kawasaki myasthenia neurology
Cor triatriatum • Epidemiology • Etiology • Associated Lesions • Differentials Diagnosis • Anatomy - Sinister,
Physiology • Clinical ... • Treatment ... Post-Operative Management ... #summary #peds ... #pediatrics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
Associated Genetic Syndromes ... palliation • Post-Op ... Tetralogy #Fallot #diagnosis ... #peds #pediatrics ... #treatment
Rheumatoid Arthritis Summary Overview: chronic, inflammatory symmetric polyarthritis involving small joints of hands/feet, knees, shoulders Signs & Symptoms:
knees, shoulders Signs ... than RF • ESR/CRP ... : CLINICAL DIAGNOSIS ... exam and imaging Treatment ... #management #rheumatology
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Males=Females SIGNS ... : Clinical diagnosis ... identified (autoimmune, meds ... , neoplastic) TREATMENT ... #management #pulmonary
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
myasthenia Diagnosis ... test - Cogan sign ... - Peek sign ... Myasthenia #Gravis #diagnosis ... #management #neurology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... : HLH signs and ... #management #treatment ... #hematology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... : • A clinical ... inflammatory changes: CRP ... and lower jaw Treatment ... diagnosis #management
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
echo is positive, treatment ... and lab signs ( ... CRP, ESR) of ongoing ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
(Clinical Dx). ... Arthritis, AS Treatment ... #diagnosis #management ... #signs #symptoms ... #rheumatology #
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
recognition and management ... HLH is a critical ... Clinical Presentation ... • Common Signs ... #Management #Hematology
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