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diagnosis management signs hematology pathophysiology aplastic arteritis differential gca giantcell hemeonc hemophagocytic henochscholeinpurpura hlh hsp iga lymphohistiocytosis myelitis neurology oncology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Clinical Presentation ... and petechiae Causes ... Sulfonamides - NSAIDs ... Idiopathic • Infections ... • Improve the symptoms
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Pathogenesis and Clinical ... Findings - Infectious ... respiratory tract infections ... Pathophysiology #Diagnosis #Signs ... #Symptoms
Polyarteritis Nodosa (PAN): Pathogenesis and Clinical Findings Medical Comorbidities Malignancies (most commonly hairy-cell leukemia) Immunogenetic Predisposition: patient is
Pathogenesis and Clinical ... Environmental triggers - Infectious ... Viral replication causes ... Pathophysiology #Diagnosis #Signs ... #Symptoms #Vasculitis
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
Transverse Myelitis - Clinical ... • Bilateral signs ... and/or symptoms ... causes need to ... - Sjogren - Vasculitis
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
systemic inflammatory vasculitis ... Diagnosis = clinical ... systemic sx + signs ... vs infection vs ... systemic complaints- anemia
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... Clinical Presentation ... • Common Signs ... and Symptoms: ... - Cytopenias (anemia
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