Lecture 18 Flashcards
Acute Myelogenous Leukemias
immature progenitor cells accumulate in bone marrow
Myelodysplastic Syndromes
ineffective hematopoiesis and resistant peripheral blood cytopenias
Chronic Myeloproliferative Disorders
Increase production of one or more terminally differentiated myeloid elements -> increased peripheral blood counts
Essential Thrombocythemia (ET)
Overproduction of platelts
Polycythemia Vera (primary polycythemia)
- Abnormality of bone marrow -> erythrocytosis (overproduction of RBCs)
- JAK2 Mutation: increase stem cell sensitivity to erythropoietin
- Symptoms: increased blood viscosity, occlusion of vessels, plethora (ruddy, red color), hypertension
Secondary Polycythemia (Erythrocytosis)
Due to prolonged hypoxia, EPO-producing tumors, Hb genetic defects, increased affinity to oxygen
Myelofibrosis
- Extensive collagen deposition by non-neoplastic fibroblasts (increased deposition of reticulin fibers) caused by neoplastic megakaryocytes
- Fibrinogenic factors PDGF and TGFB
Platelet Derived Growth Factor
Regulates fibroblast and smooth muscle cell growth and division
TGFB
Cytokine that regulates cell processes (fibrosis and tissue repair)
Chronic Myelogenous Leukemia (CML)
- neoplastic clonal expansion of bone marrow precursors
- Increased number of granulocytes
- Symptoms: night sweats, fatigue, weight loss, hypercellular bone marrow, hepatomegaly, splenomegaly
- Increased WBC, Decreased NAP (Neutrophil Alkaline Phosphatase: enzyme found in neutrophils), Decreased RBC, Increased uric acid
What are the stages of CML?
- Chronic stable phase (1-5 years)
- Accelerated/Transformation Phase (appearance of blast cells and decrease RBC and platelet counts
- Blat crisis (number of blasts in bone marrow decreases)
Acute Lymphoblastic Leukemia (ALL
Block in stem cell differentiation at early age (impacts children); acute onset; Leukemia blasts grow quickly (immature blood cells) and crowds bone marrow to prevent RBCs, WBCs, and platelet growth
Chronic Lymphocyte Leukemia (CLL)
Block in differentiation occurs later (adults); insidious onset; increase in lymphocytes with chromosomal abnormality, decreased RBCs
Hodgkin’s Disease
Malignant transformation of B cells in lymph nodes (Reed-Sternber cells); contiguous pathway
Non-Hodgkin Lymphoma
Malignant disease of lymphoid tissue (no Reed-Sternberg cells); unpredictable spread