12 results
diagnosis management rheumatology dermatology differential pruritus secondary alkaline alp arteritis common cryofibrinogenemia cutaneous cvid erythematosus eschar gca giantcell hemeonc hemophagocytic
Pruritus - Generalized Differential Diagnosis Algorithm - Systemic and Primary Causes == Primary Skin Lesions == Macules /
Pruritus - Generalized ... Primary Causes ... renal failure/uremia ... #generalized #dermatology ... #causes
Pruritus - No Primary Skin Lesion - Differential Diagnosis Algorithm Blood Glucose: • Diabetes Mellitus Liver Function Tests/Enzymes:
Pruritus - No Primary ... renal failure/uremia ... Pruritus #secondary #systemic ... #generalized #dermatology ... #causes
Hematology Algorithms Anemia is described as a reduction in the proportion of the red blood cells.
Hematology Algorithms ... Pancytopenia is a hematologic ... well as varying clinical ... Leukopenia is primarily ... These causes could
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
Vaginal dryness • Primary ... ab (specific in primary ... Hypocomplementemia • Can cause ... salivary ducts Clinical ... Nephrogenic DI Hematologic
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
particularly those coming ... Diagnosis = clinical ... complaints- anemia ... identifies 85 to 95% of cases ... them, but urgent rheumatology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Primary (essential ... processes: • Systemic ... Diagnosis: • + Clinical ... cryoglobulins • Negative causes ... #hematology
Low Alkaline Phosphatase - Hypophosphatasia Is Low Alkaline Phosphatase Of Clinical Importance? ALP enzyme- Discovered in 1923 Low
Phosphatase Of Clinical ... Adult form: Less ... • Pernicious anemia ... Phosphatase: • Other causes ... • Elevation of urinary
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... autoimmune hemolytic anemia ... ) • Systemic granulomatous ... DDX - Other causes ... hypogammaglobulinemia #immunology #hematology
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
SLE (Systemic Lupus ... ) Suspect: Clinical ... the context of primary ... lymphoproliferative syndrome Clinical ... lymphopenia, low PLT • Anemia
Polymyalgia Rheumatica (PMR) Diagnosis and Management Summary WHAT? • Polymyalgia rheumatica (PMR) is a common systemic inflammatory
PMR) is a common systemic ... disease of unknown cause ... CLINICAL: • Physical ... DIAGNOSIS: • PMR primarily ... • Normocytic anemia
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