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hematology treatment differential evaluation acromegaly anemia blood chronic common cvid deficiency dermatology disease endocrinology gastroenterology gastrointestinal hemeonc hemophagocytic hlh hypogammaglobulinemia
Gastrointestinal Evaluation of Iron Deficiency Anemia In patients with anemia, diagnose iron deficiency if: • Ferritin <
patients with anemia, diagnose ... may be needed in ... change medical management ... Gastrointestinal #Evaluation #workup ... #diagnosis #gastroenterology
Chronic Diarrhea - Workup Osmotic: • Consider food diary and trial avoiding certain foods or meds, Consider
Chronic Diarrhea ... - Workup Osmotic ... hydrogen breath test ... if performed, may ... #Workup #diagnosis
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation ... Syndrome (MAS) ... Liver function tests ... #Syndrome #Diagnosis ... #Management #Hematology
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
Clinical history: Man ... specific laboratory tests ... #management #phenotypes ... #workup #treatment ... #rheumatology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
may take 6 to 8 ... • Infectious diarrhea ... : • Nephrotic syndrome ... (Epstein-Barr syndrome ... #diagnosis #management
Pulmonary Renal Syndromes - OnePager Summary Autoimmune ANCA vasculitis (AAV): GPA (granulomatous with polyangiitis), EGPA (eosinophilic granulomatosis
Pulmonary Renal Syndromes ... mononeuritis multiplex WORKUP ... anti-GBM) Other tests ... not-optimal but may ... #management #treatment
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
and Management ... Beckwith Wiedemann syndrome ... and Workup: • ... glucose suppression test ... ACTH) 2/2 adenoma mass
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
lower-extremity joints Diagnosis ... • A clinical diagnosis ... blockers had the best ... #Rheumatology # ... diagnosis #management
Blood Product Transfusions One Pager Summary Type and screen - determines blood type and detects in recipient
indirect Coombs test ... May recur; 25% of ... cutaneous eruptions, diarrhea ... #Transfusions #diagnosis ... #management #hematology
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
recognition and management ... hyperinflammatory syndrome ... (often termed MAS-HLH ... Syndrome) 3. ... #Management #Hematology
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