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diagnosis cell cellulitis cns demyelinating differential disease diseases hematology histiocytosis idsa igg4 infections langerhans lch neurology rheumatology skin softtissue sstis
Von Willebrand Disease Classification Type 1 (Accounts for ~3/4 of cases): • Defect: Quantitative defect (i.e. not
Willebrand Disease Classification ... Qualitative defect (i.e. dysfunctional ... • Bleeding: Moderate-severe ... Bleeding: Severe (Clinically ... VonWillebrand #Disease #Classification
IDSA Algorithm for the Management of Purulent skin and soft tissue infections (SSTIs). Mild infection: for
IDSA Algorithm for ... the Management ... or those with clinical ... evidence of organ dysfunction ... including those caused
IGG-4 RELATED DISEASE WHAT? • A chronic, immune-mediated fibroinflammatory disease with tumefactive infiltration of IgG4+ plasma cells
- Organ dysfunction ... progressive organ dysfunction ... specific) COMMON CLINICAL ... • Pancreas: Type ... complement • Classification
Langerhans Cell Histiocytosis (LCH) Granulomatous Lesions comprising langerin-positive histiocytes and an inflammatory infiltrate can arise in virtually
Langerhans cells, a type ... : LCH exhibits features ... populations) CLINICAL ... • Endocrine Dysfunction ... Histiocytosis #Diagnosis #Management
DEMYELINATING DISEASES OF THE CENTRAL NERVOUS SYSTEM What Are Demyelinating Diseases? • Conditions that damage myelin, the protective
• Clinical Types ... - Symptom management ... • Features: Bilateral ... autoimmune/infectious causes ... bladder/bowel dysfunction
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