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diagnosis hemophagocytic lymphohistiocytosis treatment acromegaly classification common endocrinology hemeonc hodgkins hypogammaglobulinemia immunodeficiency immunology lymphoma oncology pathophysiology variable
Hemophagocytic Lymphohistiocytosis (HLH) Treatment Primary HLH: - HLH-94 Protocol • Dexamethasone
transplantation Secondary ... HLH: • Approach ... steroids • In mild cases ... #Treatment #management ... #hematology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
infection risk secondary ... autoimmune hemolytic anemia ... DDX - Other causes ... hypogammaglobulinemia #immunology #hematology ... #diagnosis #management
Hodgkin's Lymphoma Overview Hodgkin's lymphoma (HL) is an uncommon hematological malignancy arising from mature B cells. It
of about three cases ... Weight loss • Anemia ... Hodgkin Lymphoma Workup ... classification #hematology ... #oncology #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... STX11, STXBP2 • Secondary ... - Cytopenias (anemia ... Treatment Approach ... #Hematology #HemeOnc
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
Mortality due to CVD ... Acromegaly occurs secondary ... Diagnosis and Workup ... adenoma, ↓(TFT, LH ... or refractory cases
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