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diagnosis differential dermatology generalized management pruritus rheumatology classification cryofibrinogenemia hemeonc hemophagocytic hlh incontinence lymphohistiocytosis naildisorders polycythemia sjogrens syndrome urinary workup
Nail Disorders - Primary and Systemic Causes - Differential Diagnosis Algorithm #NailDisorders #Primary #Secondary #Systemic #dermatology #Differential
Nail Disorders - Primary ... and Systemic Causes ... #Secondary #Systemic ... #dermatology #Differential ... #causes
Types of Urinary Incontinence - Stress Incontinence - The urethral sphincter is weakened so that transient
Types of Urinary ... - Urge Incontinence ... - Overflow Incontinence ... - Incontinence Secondary ... #Causes #diagnosis
Pruritus - Generalized Differential Diagnosis Algorithm - Systemic and Primary Causes == Primary Skin Lesions == Macules /
Differential Diagnosis Algorithm ... Primary Causes ... #secondary #systemic ... #generalized #dermatology ... #causes
Polycythemia - Differential Diagnosis Algorithm Polycythemia itself isn’t a diagnosis. Like many things, it is a condition
Differential Diagnosis Algorithm ... frequently affected systems ... Better call hematology ... up EPO levels Primary ... causes: Many of
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Divided Into Two Types ... Primary (essential ... processes: • Systemic ... cryoglobulins • Negative causes ... #hematology
Pruritus - No Primary Skin Lesion - Differential Diagnosis Algorithm Blood Glucose: • Diabetes Mellitus Liver Function Tests/Enzymes:
Pruritus - No Primary ... #Pruritus #secondary ... #systemic #generalized ... #dermatology #Differential ... #causes
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
Vaginal dryness • Primary ... other diseases • Secondary ... Hypocomplementemia • Can cause ... TYPE IV RTA, TYPE ... Nephrogenic DI Hematologic
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... of the immune system ... Types of HLH • ... Primary (Familial ... STX11, STXBP2 • Secondary
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