10 results
diagnosis rheumatology treatment cell cerebritis cns cryoglobulinemia cryoglobulins differential disease erythematosus evaluation hemeonc hemophagocytic hepatology hepatopulmonary histiocytosis hlh hypertension igg4
Cryoglobulinemia Summary Cryoglobulins: • Cryoglobulins are Igs in the serum that precipitate in vitro at temperatures below
immune system, leading ... • They can cause ... Cryoglobulins Cause ... Syndrome: • Clinical ... #classification
Clinical Classification of Pulmonary Hypertension 1. Pulmonary arterial hypertension from pulmonary vasculopathy Idiopathic pulmonary arterial hypertension Heritable gene mutations
Clinical Classification ... protein receptor type ... activin A receptor type ... multifactorial mechanisms Hematologic ... #Differential #Causes
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: Severe (Clinically ... VonWillebrand #Disease #Classification ... #hematology
CNS Manifestations of Systemic Lupus Erythematosus (SLE) Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
Erythematosus (SLE) Clinical ... Encephalopathy, Cognitive Dysfunction ... autoantibodies that will cause ... inflammation, leading ... cerebritis #diagnosis #management
IGG-4 RELATED DISEASE WHAT? • A chronic, immune-mediated fibroinflammatory disease with tumefactive infiltration of IgG4+ plasma cells
- Organ dysfunction ... • Pancreas: Type ... /radiologic evidence ... complement • Classification ... #Rheumatology
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
lung disease Caused ... diffusion-perfusion defect (Type ... anatomic shunt (Type ... 2) Clinical Presentation ... 80mmHg or A-a gradient
Preoperative Risk Evaluation Major Pre-Op Questions: 1. Does the patient have any modifiable risk factors that could be
event, follow ACC algorithm ... or LV dysfunction ... Change in clinical ... What is the type ... medical and surgical management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
cytopenias and organ dysfunction ... hyperinflammatory syndrome caused ... Types of HLH • ... Clinical Presentation ... #Hematology #HemeOnc
Langerhans Cell Histiocytosis (LCH) Granulomatous Lesions comprising langerin-positive histiocytes and an inflammatory infiltrate can arise in virtually
Langerhans cells, a type ... various tissues, leading ... populations) CLINICAL ... • Endocrine Dysfunction ... Histiocytosis #Diagnosis #Management
Relapsing Polychondritis What is it? Recurrent inflammation of the cartilage in the body (Autoimmune disorder) Who? • Most frequently: 40
the most common clinical ... insufficiency • Cognitive dysfunction ... Diagnosis: • Clinical ... Antibodies to type ... #diagnosis #management
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