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diagnosis hematology management oncology photo eosinophilia anemia differential dress drugreaction signs ucsdh workup algorithm classification hemophagocytic hlh hypereosinophilia inflammatory leukemia
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Systemic Signs (DRESS Syndrome ... medication (in this case ... Images #Clinical ... #Dermatology #SkinRash ... #DRESS #Syndrome
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Systemic Signs (DRESS Syndrome ... medication (in this case ... Images #Clinical ... #Dermatology #SkinRash ... #DRESS #Syndrome
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
high WBC count cause ... Dehydration • Symptoms ... changes, stroke symptoms ... tumor burden • Symptoms ... diagnosis #management #hematology
Erythema Annulare Centrifugum (EAC), This is erythema annulare centrifugum (EAC), one of the “figurate erythemas.” These lesions
lags behind the active ... Most cases are idiopathic ... Centrifugum #EAC #clinical ... #photo #dermatology ... #skinrash
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
increased B-cell activity ... renal failure Clinical ... patients have no symptoms ... : (distinct symptoms ... ) • Löfgren syndrome
Cryoglobulinemia Summary Cryoglobulins: • Cryoglobulins are Igs in the serum that precipitate in vitro at temperatures below
• They can activate ... • They can cause ... Cryoglobulins Cause ... : • Clinical triad ... classification #rheumatology
Inherited Non-hemolytic Disorders of Hyperbilirubinemia == Disorders of Conjugation == Gilbert Syndrome: • 5-10% of the population
• Has a UGT1A1 activity ... as jaundice on clinical ... examination; nonspecific symptoms ... have no UGT1A1 activity ... and stress may cause
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
Dermatologic Manifestations ... GPA causes disease ... Rarely dominate the clinical ... • Goodpasture syndrome ... rash #diagnosis #rheumatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Constitutional Syndromes ... Aplastic Anemia Clinical ... and petechiae Causes ... • Improve the symptoms ... Anemia #oncology #hematology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... HLH signs and symptoms ... absent NK cell activity ... management #treatment #hematology
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