Leukocyte Disorders and Immune Response

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Questions and Answers

What is the primary distinction between quantitative and qualitative leukocyte disorders?

  • Quantitative disorders affect the lymphocytes, while qualitative disorders affect the granulocytes.
  • Quantitative disorders involve abnormal cell structure, while qualitative disorders affect cell number.
  • Quantitative disorders affect cell function, while qualitative disorders involve bone marrow production.
  • Quantitative disorders result from decreased production in the bone marrow, while qualitative disorders disrupt cell function. (correct)

Which condition is characterized by an elevated leukocyte count as a normal protective response to physiological stressors?

  • Neutropenia
  • Thrombocytopenia
  • Leukocytosis (correct)
  • Leukopenia

In the context of a 'shift to the left' in hematology, what does this phenomenon indicate?

  • A decreased demand for circulating mature neutrophils.
  • The bone marrow's release of immature neutrophils due to high demand for these cells. (correct)
  • An overproduction of mature erythrocytes in response to anemia.
  • An increase in the number of circulating lymphocytes during a viral infection.

Which of the following conditions is most likely associated with eosinophilia?

<p>Allergic disorders and parasitic infections (A)</p> Signup and view all the answers

Infectious mononucleosis is primarily caused by which virus?

<p>Epstein-Barr virus (EBV) (B)</p> Signup and view all the answers

Which characteristic distinguishes acute leukemia from chronic leukemia?

<p>Acute leukemia is characterized by undifferentiated or immature cells, with a rapid onset, while chronic leukemia involves more differentiated cells with a slow progression. (D)</p> Signup and view all the answers

Which environmental factor is NOT typically associated with an increased risk of developing leukemia?

<p>Exposure to pollen (A)</p> Signup and view all the answers

What is the significance of large, painless neck nodes in the context of Hodgkin lymphoma?

<p>They are a typical clinical manifestation of Hodgkin lymphoma. (C)</p> Signup and view all the answers

Non-Hodgkin lymphomas are most likely caused by what?

<p>Mutations in cellular genes, potentially environmentally induced (A)</p> Signup and view all the answers

Which of the following is a characteristic feature of Burkitt lymphoma?

<p>It is a highly aggressive B-cell lymphoma often associated with EBV. (D)</p> Signup and view all the answers

In multiple myeloma, what contributes to its poor prognosis?

<p>A wide range of genetic alterations and individual differences in responses. (A)</p> Signup and view all the answers

What hematological alteration can result from an overactive spleen?

<p>Reduction in the number of circulating blood cells (D)</p> Signup and view all the answers

What percentage of the red blood cell population can the spleen potentially sequester, leading to anemia?

<p>50% (B)</p> Signup and view all the answers

What does localized lymphadenopathy typically suggest?

<p>Drainage of an area associated with inflammation, infection, or malignancy (A)</p> Signup and view all the answers

Which of the following best describes generalized lymphadenopathy?

<p>Enlargement of lymph nodes throughout the body, typically due to systemic disease. (A)</p> Signup and view all the answers

Flashcards

Leukocytosis

Increased leukocyte count, a normal protective response to stressors.

Neutrophilia

Increase in granulocytes, especially neutrophils, released from bone marrow.

Shift to the left

Immature neutrophils released due to high demand, indicated by increased immature leukocytes.

Eosinophilia

Absolute increase in circulating eosinophils, often linked to allergic reactions or parasitic infections.

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Monocytosis

Increase in circulating monocytes, commonly associated with bacterial infection.

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Lymphocytosis

Increase in lymphocytes, typically seen in acute viral infections.

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Infectious Mononucleosis (IM)

Acute viral infection of B lymphocytes caused by EBV, transmitted through saliva.

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Leukemia

Disorder of leukocytes in bone marrow with uncontrolled proliferation of malignant leukocytes.

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Acute Leukemia

Leukemia with undifferentiated or immature cells, abrupt onset, and rapid progression.

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Chronic Leukemia

Leukemia with more differentiated cells, slow progression, and abnormal cell function.

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Lymphadenopathy

Increase in size and number of germinal centers of the lymph node.

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Lymphoma

Proliferation of malignant lymphocytes in the lymphoid system.

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Hodgkin Lymphoma

Type of lymphoma derived from a B cell in the germinal center.

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Burkitt Lymphoma

Aggressive B-cell non-Hodgkin lymphoma, often linked to EBV.

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Hypersplenism

Hematologic alterations due to an overactive spleen, reducing circulating blood cells.

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Study Notes

Leukocyte Disorders

  • Categorized as either quantitative or qualitative.
  • Quantitative disorders result from decreased bone marrow production.
  • Qualitative disorders involve disrupted cell function.

Leukocytosis

  • Leukocyte count is higher than normal.
  • Normal protective response to stressors like infection, exercise, emotional changes, temperature changes, anesthesia, pregnancy, drugs, hormones, and toxins.

Neutrophilia

  • Describes granulocytosis.
  • Neutrophils are the most numerous granulocytes.

Cranial Psychosis

  • Increase in granulocytes released from bone marrow.

Shift to the Left (Leftward Shift)

  • Demand for mature neutrophils exceeds supply.
  • Bone marrow releases immature neutrophils.
  • Increases immature leukocytes number in blood.

Eosinophilia

  • Absolute increase in circulating eosinophils.
  • Associated with allergic disorders like asthma, hay fever, and drug reactions, also parasitic infections.

Monocytosis

  • Increase in circulating monocytes number.
  • Commonly linked to bacterial infection.

Lymphocytosis

  • Occurs most commonly in acute viral infections.

Infectious Mononucleosis (IM)

  • Benign, acute, self-limiting lymphoproliferative clinical syndrome.
  • Caused by acute viral infection of B lymphocytes.
  • Caused by EBV, a type of herpes virus.
  • EBV transmitted usually by saliva through personal contact (kissing disease).

Leukemia

  • Disorder of leukocytes in bone marrow, and usually blood.
  • Uncontrolled proliferation of malignant leukocytes.
  • Decreased production and function of normal hematopoietic cells.
  • Acute leukemia: undifferentiated or immature cells, abrupt and rapid onset, short survival time.
  • Chronic leukemia: more differentiated cells, not functioning normally, relatively slow progression.
  • Acute leukemias: acute lymphocytic leukemia (ALL) and acute myelogenous leukemia (AML).
  • ALL: aggressive, fast-growing leukemia with too many lymphoblasts.
  • AML: aggressive, fast-growing leukemia with excessive myeloblasts in bone marrow and blood.
  • Chronic leukemias: chronic myelogenous leukemia (CML) and chronic lymphocytic leukemia (CLL).
  • CLL: slow-growing cancer with too many immature lymphocytes, mainly in bone and bone marrow.
  • Leukemia reappearance statistically significant in families.
  • Increased risk in adults with exposure to cigarette smoke, benzene, and ionizing radiation.

Lymphoma

  • Lymphadenopathy: increase in size and number of lymph node germinal centers.
  • Large neck nodes are characterized by being palpable and often tender.
  • Localized lymphadenopathy: drainage of area with inflammation, or infection.
  • Generalized lymphadenopathy: result of malignant or non-malignant disease.
  • Lymphomas develop from proliferation of malignant lymphocytes in lymphoid system.
  • Hodgkin and non-Hodgkin lymphoma occur in children and adults.
  • Hodgkin lymphoma: derived from B cell in germinal center that has not undergone successful immune immunoglobulin gene rearrangement.
  • Hodgkin lymphoma clinical manifestations: fever, weight loss, night sweats, pruritus, fatigue, large, painless neck.
  • Non-Hodgkin's lymphoma manifestations: progressive clonal expansion of B-cells, T cells, and natural killer cells.
  • Non-Hodgkin's lymphomas most likely caused by mutations in cellular genes, possibly environmentally induced.
  • Burkitt lymphoma: aggressive B-cell non-Hodgkin lymphoma (30% of childhood lymphomas worldwide).
  • EBV associated with almost all cases.
  • Lymphoblastic lymphoma: rare variant of non-Hodgkin lymphoma (2-4% incidence).

Multiple Myeloma

  • Biologically complex disease with wide range of genetic alterations and individual differences in responses.
  • Has poor prognosis.
  • Median survival is three years.
  • Untreated individuals with multiple bone lesions rarely survive more than 6 to 12 months.

Splenic Function

  • Splenomegaly seen in 7-15% of individuals.
  • Overactive spleen results in hematologic alterations.
  • Overactive spleen causes a reduction in circulating blood cells.
  • Spleen can sequester up to 50% of red blood cell population, potentially creating anemia.

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