Hematology

Cards (67)

  • Chronic Lymphoproliferative Disorders

    • Chronic Lymphocytic Leukemia
    • Pro-Lymphocytic Leukemia
    • Hairy Cell Leukemia
  • Chronic Lymphocytic Leukemia
    • Predominant cell: Dormant B-cells (cannot produce antibodies)
    • Less likely to undergo blastic transformation (chronic- acute)
    • Chronic Granulocytic L- can undergo blastic T.
    • Autoimmune Hemolytic Anemia- hemolysis (presence of autoantibodies)
  • Autoantibodies
    Cell antibodies, can react with RBC> Complement activated= HEMOLYSIS (decreased RBC count)
  • Other Signs and Symptoms of Chronic Lymphocytic Leukemia
    • Lymphadenopathy (enlargement of lymph nodes)
    • Splenomegaly (enlargement of spleen why= hemolysis)
    • Hepatomegaly
    • Pruritus- skin infection caused by Herpes zoster
  • Reason for skin infection in Chronic Lymphocytic Leukemia
    No antibodies
  • Lab Findings for Chronic Lymphocytic Leukemia
    • Lymphocyte count: 10-150x 10^9/L
    • PBS: predominant of SMUDGE cells(T cells)
    • Hypogammaglobulinemia (decreased antibodies)
  • Prognosis for Chronic Lymphocytic Leukemia
    1. 4 years
  • Treatment for Chronic Lymphocytic Leukemia
    Leukapheresis (transfusion of granulocytes as well as WBC) and regular injection with IgG (additional AB)
  • Hairy Cell Leukemia/ Lymphocytic Reticuloendotheliosis
    • Affected cell: B-cells
    • Pancytopenia (increased in all blood cells)
    • Splenomegaly- Splenectomy (removal of spleen)
  • Characteristics of Hairy Cell Leukemia
    • 40-60 yrs old (Males 4x more prone)
  • TRAP
    Tartrazine Resistant Acid Phosphatase
  • Acid Phosphatase
    Common seen in prostate (seminal fluid)
  • Pro-Lymphocytic Leukemia
    • Predominant cells: prolymphocytes
    • Increase promyelocytes
  • Prognosis for Pro-Lymphocytic Leukemia
    < 1 year
  • Other Lymphocytic Neoplasms
    • Infection/viruses
  • Burkitt's Lymphoma
    • EBV and HIV
    • Translocation of c-myc on chromosome region
  • Mycosis Fungoides and Sezary Syndrome
    • Different stages of a single neoplastic disorder (neoplastic: new cells(abnormal))
    • T-helper cell (lymphatic tissues) – skin
    • Skin: parakeratosis
    • Pautrier's microabscesses (lymphocyte clusters)
    • Lymph node: Sezary cells
    • Band-like infiltrates
  • Plasma cell
    B lymphocytes (ANTIBODIES)
  • Multiple Myeloma
    • Plasma cell Dysfunctional
    • 50% of IgG
    • 20% of IgA
    • 15% of lambda and gamma chain
    • Abnormal protein (BENCE JONES PROTEINS) not excreted = tends to accumulate; present in 80% of MM px
  • How to know if there are BJP in the urine
    Test for solubility (heat at 60-80C= will form precipitate) 150C- DISSOLVE
  • Hyaline cast

    First cast that will form, made up of uromodulin/Tamm–Horsfall protein
  • Types of chains in Multiple Myeloma
    • Light chain (lambda, gamma), gamma chain
  • Increased Protein
    RBC form roulex formation
  • ESR
    Elevated/ Increased
  • Flame cells
    With reddish tinge of ribosomal proteins (IgA)
  • Dutcher bodies
    Intranuclear crystalline structures (IgG)
  • Russel Bodies
    Accumulations of IgG
  • Grape cell/Mott cell, Morula cell

    Plasma cell that contains small colorless/ blue/ pink globules
  • Plasma Cell Leukemia
    >2x10^9/L plasma cell count
  • Waldenstroms Macroglobulinemia
    • Increase production of IgM (>3 g/dL); Increase protein= Rouleux formation= Increase ESR
  • Heavy Chain Disease
    • Abnormal synthesis (Gamma(IgG) or Alpha(IgA))
  • Causes of Lymphoma
    • Infections (part. HIV/EBV)
    • Enlargement of the lymph nodes
  • Signs and Symptoms of Hodgkin's Lymphoma
    • Fever
    • Night sweats or 10% weight loss in 6 months (it can be both)
    • Leukocytosis
    • Lymphocytopenia
  • Leukocytosis
    Increased in all WBC
  • Lymphocytopenia
    Decrease lymphocytes
  • Prognosis of Hodgkin's Lymphoma with Lymphocytopenia
    Poor prognosis
  • Diagnosis of Hodgkin's Lymphoma

    Lymph node biopsy (histopath) – presence of REED- STERNBERG CELL (lacunar histiocytes)
  • Reed-Sternberg cell
    Giant multi/binucleated cell- hallmark finding for Hodgkin's lymphoma
  • Ann Harbor Staging System for Hodgkin's Lymphoma
    • I-IV (locate region of lymph nodes)
    • A(no symptom) or B(presence of symptom (suffix)
    • E (extra lymphatic involvement- organs affected) or S(spreading) (subscripts)
  • Stage 1 Hodgkin's Lymphoma
    • Single lymph node is affected (axillary area)