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diagnosis hematology treatment hemophagocytic lymphohistiocytosis acromegaly activation cvid endocrinology hemeonc hepatopulmonary hypogammaglobulinemia immunodeficiency immunology macrophage mas pathophysiology rheumatology variable
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... symptoms can mimic common ... lymph node, or liver ... Lymphohistiocytosis #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Clinical Presentation ... Fever is the main clinical ... • HLH Labs: ... thrombocytopenia • Liver ... #Diagnosis #Management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
HLH is a critical ... : - Common in ... Clinical Presentation ... • Common Signs ... - Elevated liver
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... disease • Liver ... : • Nephrotic syndrome ... (Epstein-Barr syndrome ... #diagnosis #management
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
Hepatopulmonary Syndrome ... shunt (Type 2) Clinical ... • Dyspnea - Common ... hepatopulmonary #syndrome ... #treatment #hepatology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
Diagnosis and Management ... GrepMed Handbook Clinical ... GH stimulates liver ... Beckwith Wiedemann syndrome ... adenoma, ↓(TFT, LH
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