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PLACO Mnemonic - Approach to Acid-Base Disorders
P - Determine the pH
L - Labs: PCO2 & HCO3
A
PLACO Mnemonic - Approach to Acid-Base Disorders P - Determine the pH L - Labs: PCO2 & HCO3 A - Calculate Anion Gap C - Compensation O - Other Processes Paresh Jadav, MD @jadav_md #PLACO #AcidBase #Acid #Base #diagnosis #nephrology #Mnemonic
Lymphoid Neoplasms

Hodgkin Lymphomas vs Non-Hodgkin Lymphomas

Andrew Sanchez M.D. @ASanchez_PS

#Lymphoid #Hodgkin #Lymphoma #NonHodgkin #diagnosis #oncology
Lymphoid Neoplasms Hodgkin Lymphomas vs Non-Hodgkin Lymphomas Andrew Sanchez M.D. @ASanchez_PS #Lymphoid #Hodgkin #Lymphoma #NonHodgkin #diagnosis #oncology
Thrombocytopenia - Differential Diagnosis Algorithm

Decreased production:
 • Bone marrow suppression
 • Bone marrow failure
 • Bone
Thrombocytopenia - Differential Diagnosis Algorithm Decreased production: • Bone marrow suppression • Bone marrow failure • Bone marrow infiltration • Infection • Nutritional Increased destruction/consumption: • Connective tissue disorders • Immune destruction • Consumption • Destruction Matthew Ho, MD PhD @MatthewHoMD #Thrombocytopenia #Differential #Diagnosis #Algorithm #hematology #platelets
Aplastic Anemia - Overview

Who?
• M = F
• 3 peaks:	1) Childhood	2) 15-25 years	3) >60 years

What?
• Aplastic anemia
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia = Hypocellular bone marrow + pancytopenia Mechanisms: • Direct Damage to Marrow (Toxic injury to BM) • Constitutional Syndromes (specific loss-of-function germline mutations) • Immune Aplastic Anemia Clinical Presentation: • Fever • Fatigue • Lightheadedness • Dizziness • Irritability • Headaches • Pale skin color • Difficulty breathing • Neutropenia - recurrent infections/fevers • Thrombocytopenia - ecchymoses, mucosal bleeding, and petechiae Causes: • Constitutional Syndromes: - Genetic lesions that diminish the capacity for hematopoietic stem cells to repair DNA, as in Fanconi anemia, GATA2 deficiency, CTLA4 deficiency, Dyskeratosis congenita • Drugs: - Cytotoxic drugs/Chemotherapy - Antithyroid medications (methimazole and propylthiouracil) - β-lactam antibiotics - Sulfonamides - NSAIDs - Anticonvulsants - Gold salts • Chemical Agents: - Benzene • Physical Agents: - Radiation • Idiopathic • Infections: - Parvovirus B19 - EBV - CMV - HCV - HIV • Immune Aplastic Anemia: - Hepatitis, eosinophilic fasciitis, and thymoma DDX: • Inherited marrow-failure syndromes • Paroxysmal nocturnal hemoglobinuria • Hypocellular myelodysplastic syndrome (MDS) (normal or increased number of CD34+ cells) • Human immunodeficiency virus (HIV) • Parvovirus B19 • Mycobacteria • Cytomegalovirus (CMV) • Epstein-Barr virus (EBV) • Leukemia Hypocellular/Hypoplastic MDS: • ↓ bone marrow cellularity + dysplastic cells + cytogenetic abnormalities typical for MDS • Suggested by bone marrow with dysplastic megakaryocytes and a normal or increased number of CD34+ cells (not consistent with aplastic anemia) Labs: • Peripheral Pancytopenia: • ↓ RBC • ↓ WBC • ↓ PLT • Reticulocyte index < 2 • EPO Level ↑ • Marrow hypoplasia/fatty bone marrow • Number of CD34+ cells is much reduced in aplastic anemia Treatment: • Improve the symptoms that may result from low blood counts • Allogeneic HSCT for younger than 50 years who have a suitable match • Immunosuppression - cyclosporine and antithymocyte globulin #Aplastic #Anemia #oncology #hematology #diagnosis #management