p.6
Hemolytic Anemias and Their Classifications
What are examples of extracorpuscular defects in Hemolytic Anemias?
Mechanical destruction (microangiopathic), Toxic agents, Infectious, Autoimmune.
p.6
Hemolytic Anemias and Their Classifications
What is the distinguishing feature of Iron Deficiency Anemia?
Microcytic hypochromic anemia with low serum ferritin.
p.6
Bleeding Disorders and Coagulation Profiles
What is the effect of Vitamin K Deficiency on bleeding profiles?
Normal PT, Normal PTT, Prolonged bleeding time.
p.2
Histopathologic Findings in Hematologic Diseases
What cells in adult T-cell lymphoma appear to have multi-lobulated nuclei?
Cloverleaf or flower cells.
p.4
Lymphoma Types and Characteristics
What is the most common type of Non-Hodgkin's Lymphoma?
Diffuse large B-cell lymphoma.
p.6
Hemolytic Anemias and Their Classifications
What is the primary cause of Aplastic Anemia?
Pancytopenia with bone marrow hypocellularity.
p.6
Hemolytic Anemias and Their Classifications
What are examples of intracorpuscular defects in Hemolytic Anemias?
Hemoglobinopathies, Enzymopathies, Membrane cytoskeletal defects.
p.3
Acute and Chronic Leukemias
What are smudge cells associated with?
Chronic lymphocytic leukemia (CLL).
p.5
Histopathologic Findings in Hematologic Diseases
What is the histopathologic finding associated with Hereditary Spherocytosis?
Small hyperchromic RBCs lacking spherocytes.
p.5
Hemolytic Anemias and Their Classifications
What is the triad of hemolytic anemia?
Anemia, jaundice, and splenomegaly.
p.5
Hemolytic Anemias and Their Classifications
What is a telltale sign of intravascular hemolysis?
Hemoglobinuria (often associated with hemosiderinuria).
p.6
Bleeding Disorders and Coagulation Profiles
What is the impact of Disseminated Intravascular Coagulation (DIC) on bleeding profiles?
Decreased platelet count, Prolonged PT, Prolonged PTT.
p.3
Acute and Chronic Leukemias
What is associated with non-contiguous spread in lymphoma?
Non-Hodgkin's lymphoma (NHL).
p.4
Lymphoma Types and Characteristics
What type of Hodgkin's Lymphoma has the best prognosis?
Lymphocyte-rich mononuclear variant.
p.3
Acute and Chronic Leukemias
Which leukemia is primarily a disease of older adults?
Chronic lymphocytic leukemia.
p.4
Plasma Cell, Thymus and Spleen Disorders
What are Bence-Jones proteins?
Excess light or heavy chains synthesized by neoplastic plasma cells.
p.4
Plasma Cell, Thymus and Spleen Disorders
What are the clinical features of Multiple Myeloma?
Hypercalcemia, renal involvement, anemia, and lytic lesions.
p.6
Bleeding Disorders and Coagulation Profiles
What is the characteristic of Immune Thrombocytopenic Purpura (ITP) in bleeding disorders?
Decreased platelet count, Normal PT, Normal PTT.
p.2
Histopathologic Findings in Hematologic Diseases
What histopathologic finding is associated with severe infection and appears as sky blue cytoplasmic puddles?
Patches of dilated endoplasmic reticulum that appear as Diihle bodies.
p.5
Histopathologic Findings in Hematologic Diseases
What are Schistocytes and in which conditions are they found?
Fragmented RBCs found in MAHAs like DIC, TTP/HUS, HELLP syndrome.
p.2
Histopathologic Findings in Hematologic Diseases
What is the term for megakaryocytes with single nuclear lobes or multiple separate nuclei?
Pawn ball megakaryocytes in Myelodysplastic syndrome.
p.3
Acute and Chronic Leukemias
What type of acute myeloid leukemia has the best prognosis?
Acute promyelocytic leukemia (APL) with t(15;17).
p.3
Acute and Chronic Leukemias
What is the cutoff blast percentage for diagnosing AML?
20% in peripheral blood and bone marrow.
p.2
Histopathologic Findings in Hematologic Diseases
What type of cells are characterized by only two nuclear lobes?
Pseudo-Pelger-Huet cells.
p.1
Iron Transport and Storage Proteins
What is hemosiderin?
A supplemental storage protein for iron.
p.3
Acute and Chronic Leukemias
What chromosome abnormality is associated with chronic myeloid leukemia?
t(9;22) (Philadelphia chromosome).
p.6
Hemolytic Anemias and Their Classifications
What leads to the distinctive morphologic changes in Megaloblastic Anemia?
Impairment of DNA synthesis.
p.2
Histopathologic Findings in Hematologic Diseases
What type of cells are characterized by bilobed nuclei and prominent Reed-Sternberg inclusions?
Giant 8 cells in Hodgkin's lymphoma.
p.5
Hemolytic Anemias and Their Classifications
What is Microangiopathic Hemolytic Anemia associated with?
DIC, TTP-HUS, SLE, and malignant hypertension.
p.7
Hemolytic Anemias and Their Classifications
What is Methemoglobin?
Oxidation of the heme component of hemoglobin to iron which cannot bind oxygen.
p.3
Acute and Chronic Leukemias
What is a common CBC finding in chronic myeloid leukemia?
WBC usually > 100,000/mm³ of immature granulocytic cells.
p.5
Hemolytic Anemias and Their Classifications
What condition is characterized by intravascular hemolysis due to increased complement-mediated RBC lysis?
Paroxysmal Nocturnal Hemoglobinuria.
p.1
Fetal Erythropoiesis Stages
What are reticulocytes?
Immature RBC released by the bone marrow into the blood.
p.2
Histopathologic Findings in Hematologic Diseases
What are the cells called that were probably damaged during the birthing process in fibrotic marrow?
Teardrop cells or dacrocytes.
p.1
Platelet Function and Disorders
What is required for platelet aggregation?
Glycoprotein IIb-IIIa and fibrinogen.
p.3
Acute and Chronic Leukemias
What is the most common cancer in children?
Acute lymphoblastic leukemia.
p.4
Plasma Cell, Thymus and Spleen Disorders
What condition is a tumor of the thymus associated with?
Myasthenia gravis and pure red cell aplasia.
p.5
Histopathologic Findings in Hematologic Diseases
What condition is associated with target cells?
HbC disease, Asplenia, Liver disease, Thalassemia.
p.1
Fetal Erythropoiesis Stages
What is the last stage of RBC that contains a nucleus?
Orthochromatic erythroblast.
p.2
Histopathologic Findings in Hematologic Diseases
What histopathologic finding is characterized by pentalaminar tubules with a dilated terminal end?
Langerhans cell histiocytosis.
p.4
Lymphoma Types and Characteristics
What chromosomal translocation is associated with Burkitt's lymphoma?
Translocation between chromosomes 8 and 14.
p.7
Hemolytic Anemias and Their Classifications
What is Fetal Hemoglobin composed of?
A tetramer consisting of two alpha and gamma chains.
p.3
Acute and Chronic Leukemias
What should raise suspicion of myelodysplastic syndrome?
Refractory anemia not attributed to any other cause.
p.5
Histopathologic Findings in Hematologic Diseases
What are Burr cells associated with?
Liver disease, abetalipoproteinemia, vitamin E deficiency.
p.1
Platelet Function and Disorders
What is required for platelet adhesion?
Glycoprotein lb and von Willebrand Factor.
p.5
Histopathologic Findings in Hematologic Diseases
What are Heinz bodies associated with?
G6PD deficiency due to damaged membranes.
p.3
Acute and Chronic Leukemias
What symptoms are common in both Hodgkin's and Non-Hodgkin's lymphoma?
Low-grade fever, night sweats, weight loss.
p.1
Fetal Erythropoiesis Stages
What is the last stage of RBC capable of mitosis?
Polychromatic erythroblast.
p.7
Hemolytic Anemias and Their Classifications
What are Hemoglobin Barts?
Gamma-tetramers found in newborns.
p.1
Immunoglobulin Classes and Functions
What is the function of IgA?
Found in secretions (e.g., saliva, Peyer's patches).
p.5
Hemolytic Anemias and Their Classifications
What disorder is caused by intrinsic defects in the red cell membrane?
Hereditary Spherocytosis.
p.7
Hemolytic Anemias and Their Classifications
What is Carboxyhemoglobin?
A form of hemoglobin where CO binds tightly but reversibly.