Chapter 24: Leukemia Flashcards
A 3-year-old boy is brought to the pediatric clinic with complaints of fatigue, fever, and bruising. His mother states he has been unusually irritable and has developed multiple nosebleeds over the past few weeks. A complete blood count (CBC) reveals anemia, thrombocytopenia, and leukocytosis with blasts.
Based on the clinical presentation and lab findings, what is the most likely diagnosis?
A. Acute lymphoblastic leukemia (ALL)
B. Acute myelogenous leukemia (AML)
C. Chronic myelocytic leukemia (CML)
D. Iron-deficiency anemia
A. Acute lymphoblastic leukemia (ALL)
Rationale: Fatigue, fever, bruising, and nosebleeds are hallmark signs of ALL, which is the most common leukemia in children aged 2–3 years. The CBC findings of anemia, thrombocytopenia, and blast cells also support the diagnosis of ALL.
Rasheed, a 12-year-old boy diagnosed with ALL, is beginning chemotherapy. During an assessment, the nurse notes that Rasheed appears pale and has a fever of 101.3°F (38.5°C). His mother reports he has been complaining of a sore throat. What is the nurse’s priority intervention?
A. Administer acetaminophen to reduce the fever.
B. Assess Rasheed’s complete blood count and notify the oncologist.
C. Provide oral hygiene instructions to prevent infection.
D. Encourage Rasheed to rest and increase fluid intake.
B. Assess Rasheed’s complete blood count and notify the oncologist.
Rationale: Fever and sore throat in a child with ALL undergoing chemotherapy may indicate neutropenia and infection, requiring immediate assessment of CBC and prompt medical intervention.
Which child is at the highest risk for developing acute lymphoblastic leukemia (ALL)?
A. A 2-year-old African American girl
B. A 14-year-old Hispanic boy
C. A 1-year-old Asian girl
D. A 3-year-old White boy
D. A 3-year-old White boy
Rationale: ALL is most common in White children, with a peak age of onset between 2 and 3 years. It also occurs more frequently in boys.
A 15-month-old girl is diagnosed with acute myelogenous leukemia (AML). Her parents ask the nurse how this condition differs from acute lymphoblastic leukemia (ALL). Which statement by the nurse provides the best explanation?
A. “ALL affects lymphoid cells, while AML affects myeloid cells.”
B. “AML is more common in school-age children, while ALL occurs mostly in infants.”
C. “AML has a higher survival rate compared to ALL.”
D. “ALL progresses more slowly than AML in children.”
A. “ALL affects lymphoid cells, while AML affects myeloid cells.”
Rationale: ALL arises from lymphoid cells, while AML arises from myeloid cells. AML is less common but occurs more frequently in infants and adolescents.
What is the primary reason children with leukemia often present with anemia and thrombocytopenia?
A. Chemotherapy suppresses the bone marrow.
B. Increased infections lead to destruction of red blood cells and platelets.
C. Leukemic cells inhibit the production of healthy blood cells.
D. A vitamin deficiency caused by leukemia reduces blood cell production.
C. Leukemic cells inhibit the production of healthy blood cells.
Rationale: Leukemic cells proliferate in the bone marrow, reducing the production of normal red blood cells and platelets, leading to anemia and thrombocytopenia.
A 16-month-old child with AML is receiving chemotherapy. The parents report that the child has been vomiting frequently and is unable to tolerate oral intake. What is the priority nursing intervention?
A. Administer antiemetics as prescribed and monitor fluid balance.
B. Encourage the parents to offer small, frequent meals.
C. Begin oral rehydration therapy to replace lost fluids.
D. Schedule a feeding tube placement.
A. Administer antiemetics as prescribed and monitor fluid balance.
Rationale: Antiemetics should be administered to reduce chemotherapy-induced nausea and vomiting. Fluid balance must be closely monitored to prevent dehydration.
Which of the following is a distinguishing characteristic of acute lymphoblastic leukemia (ALL) compared to acute myelogenous leukemia (AML)?
A. ALL is more common in adolescents, while AML is more common in young children.
B. ALL is more common in African Americans, while AML is more common in Whites.
C. ALL has a lower survival rate compared to AML.
D. ALL arises from lymphoid cells, while AML arises from myeloid cells.
D. ALL arises from lymphoid cells, while AML arises from myeloid cells.
Rationale: ALL arises from lymphoid cells, whereas AML originates from myeloid cells. ALL is more common in younger children, and AML is more common in infants and adolescents.
A 6-year-old boy presents with fatigue, recurrent infections, and nosebleeds. Laboratory results reveal anemia, thrombocytopenia, and leukocytosis with a high percentage of immature white blood cells. His medical history is significant for Down syndrome.
Based on the child’s medical history and clinical findings, which condition is most likely contributing to his symptoms?
A. Iron-deficiency anemia
B. Acute lymphoblastic leukemia (ALL)
C. Idiopathic thrombocytopenic purpura (ITP)
D. Acute myelogenous leukemia (AML)
B. Acute lymphoblastic leukemia (ALL)
Rationale: Children with Down syndrome are at a significantly increased risk of developing ALL. Symptoms such as fatigue, infections, and bleeding, along with lab results showing anemia, thrombocytopenia, and leukocytosis with blasts, are hallmark findings of leukemia.
A 4-year-old girl with a history of Wiskott-Aldrich syndrome presents with fever, bruising, and pallor. A bone marrow biopsy confirms acute lymphoblastic leukemia (ALL). What underlying condition most likely predisposed the child to ALL?
A. A previous history of ionizing radiation exposure
B. Congenital immune deficiency
C. Neurofibromatosis type I
D. Chemotherapy treatment for a prior cancer
B. Congenital immune deficiency
Rationale: Wiskott-Aldrich syndrome is a congenital immune deficiency that increases the risk of developing ALL.
Which chromosomal abnormality is associated with an increased risk of developing acute lymphoblastic leukemia (ALL)?
A. Turner syndrome
B. Klinefelter syndrome
C. Fragile X syndrome
D. Down syndrome
D. Down syndrome
Rationale: Down syndrome is associated with a significantly increased incidence of ALL, as well as other hematologic malignancies.
A 7-year-old boy with a history of chemotherapy treatment for retinoblastoma is now diagnosed with acute myelogenous leukemia (AML). What is the most likely etiology of his leukemia?
A. Genetic predisposition
B. Previous exposure to ionizing radiation
C. Previous chemotherapy treatment
D. Congenital chromosomal defect
C. Previous chemotherapy treatment
Rationale: Chemotherapy treatment for other cancers is a known risk factor for the development of AML.
Which of the following explains the increased susceptibility to infections in children with leukemia?
A. Malignant WBCs are immature and cannot perform normal immune functions.
B. Immature WBCs crowd out platelets, reducing clotting ability.
C. Bone marrow fails to produce enough hemoglobin for oxygen transport.
D. Abnormal WBCs increase the risk of autoimmune disorders.
A. Malignant WBCs are immature and cannot perform normal immune functions.
Rationale: In leukemia, immature WBCs proliferate abnormally, replacing normal WBCs and reducing the body’s ability to fight infections.
A 5-year-old boy presents with petechiae, fatigue, and recurrent infections. Lab results reveal pancytopenia and the presence of leukemic blasts. The nurse understands that these findings are caused by:
A. Destruction of healthy blood cells by malignant WBCs.
B. Increased production of abnormal platelets by the bone marrow.
C. Replacement of normal stem cells in the bone marrow by leukemic cells.
D. Infiltration of the spleen and liver by abnormal WBCs.
C. Replacement of normal stem cells in the bone marrow by leukemic cells.
Rationale: Leukemic cells in the bone marrow replace normal stem cells, leading to pancytopenia, which manifests as anemia, thrombocytopenia, and increased infection risk.
Which of the following syndromes is most likely associated with an increased risk of acute myelogenous leukemia (AML)?
A. Neurofibromatosis type I
B. Shwachman syndrome
C. Ataxia-telangiectasia
D. Bloom syndrome
A. Neurofibromatosis type I
Rationale: Neurofibromatosis type I is associated with an increased risk of AML, among other hematologic malignancies.
A newborn with a history of Bloom syndrome develops petechiae and ecchymosis. A bone marrow biopsy reveals acute lymphoblastic leukemia (ALL).
What aspect of the child’s history likely contributed to this condition?
A. Immune deficiency associated with Bloom syndrome
B. Exposure to maternal chemotherapy in utero
C. Ionizing radiation exposure during pregnancy
D. Familial history of leukemia
A. Immune deficiency associated with Bloom syndrome
Rationale: Bloom syndrome, a congenital condition characterized by chromosomal instability, increases the risk of developing ALL.
Why are children with leukemia at increased risk for anemia?
A. Increased destruction of erythrocytes by leukemic cells
B. Reduced erythrocyte production due to overcrowding of the bone marrow by leukemic cells
C. Chronic blood loss caused by gastrointestinal bleeding
D. Hemolysis caused by chemotherapy
B. Reduced erythrocyte production due to overcrowding of the bone marrow by leukemic cells
Rationale: Leukemic cells rapidly proliferate in the bone marrow, replacing normal stem cells, which leads to decreased erythrocyte production and anemia.
A 10-year-old boy undergoing evaluation for fatigue and bruising is diagnosed with leukemia. His lab results include low platelets and abnormal leukocytes. His parents ask why he is bruising so easily. Which explanation is most appropriate?
A. “The cancer is causing your son’s blood vessels to become fragile.”
B. “The abnormal white blood cells are attacking healthy platelets.”
C. “Infections caused by leukemia are damaging your son’s platelets.”
D. “Leukemia reduces the number of platelets needed for blood clotting.”
D. “Leukemia reduces the number of platelets needed for blood clotting.”
Rationale: Leukemia reduces platelet production because the bone marrow is overcrowded with leukemic cells, which leads to bruising and other bleeding abnormalities.
A 4-year-old girl presents with fever, anorexia, and pallor. Upon examination, her spleen and liver are enlarged. Her parents report she has been experiencing persistent joint pain. What diagnostic step should be prioritized to confirm leukemia?
A. Lumbar puncture
B. Bone marrow aspiration
C. Complete blood count with differential
D. Abdominal ultrasound
B. Bone marrow aspiration
Rationale: Bone marrow aspiration is the definitive diagnostic test for leukemia, allowing direct observation of leukemic cell proliferation in the bone marrow.
A child diagnosed with ALL develops a new symptom: difficulty moving their left eye laterally. Which cranial nerve is most likely affected?
A. Third cranial nerve
B. Fourth cranial nerve
C. Sixth cranial nerve
D. Seventh cranial nerve
C. Sixth cranial nerve
Rationale: The sixth cranial nerve controls lateral eye movement. Leukemic cell massing in the CNS can put pressure on this nerve, causing palsy and restricted lateral movement of the eye.
A 10-year-old boy presents with fever, lethargy, pallor, and joint pain. On physical examination, petechiae and hepatosplenomegaly are noted. Which finding would most strongly suggest infiltration of leukemia into the central nervous system?
A. Lymphadenopathy
B. Enlarged testicles
C. Papilledema
D. Sixth cranial nerve palsy
D. Sixth cranial nerve palsy
Rationale: Sixth cranial nerve palsy, characterized by the inability to move the eye laterally, is a specific sign of CNS infiltration by leukemic cells.
A 6-year-old boy is diagnosed with acute lymphoblastic leukemia (ALL). His parents report that he has been experiencing bone pain and has difficulty walking. Which pathophysiological process explains his symptoms?
A. Bone marrow expansion due to leukemic cell proliferation
B. Infiltration of leukemic cells into the central nervous system
C. Reduced production of erythrocytes leading to hypoxia
D. Autoimmune destruction of healthy bone cells
A. Bone marrow expansion due to leukemic cell proliferation
Rationale: Proliferation of leukemic cells in the bone marrow can cause expansion and pressure within the bone, leading to pain and difficulty walking.
A child with AML presents with painless enlargement of the testicles. What is the most likely underlying cause of this manifestation?
A. Inflammation due to leukemic cell activity
B. Hematoma formation from thrombocytopenia
C. Tumor formation from leukemic cell infiltration
D. Hypoxia-induced swelling
C. Tumor formation from leukemic cell infiltration
Rationale: Leukemic cells can infiltrate the testicles, leading to the formation of a painless mass and subsequent enlargement of the testicle.
A 12-year-old girl with ALL has been experiencing persistent headaches and vomiting. On examination, papilledema is observed. What is the most likely explanation for her symptoms?
A. Dehydration due to anorexia
B. Infiltration of leukemic cells into the CNS causing increased intracranial pressure
C. Hepatosplenomegaly leading to systemic inflammation
D. Side effect of chemotherapy
B. Infiltration of leukemic cells into the CNS causing increased intracranial pressure
Rationale: CNS infiltration by leukemic cells can lead to increased intracranial pressure, causing symptoms such as headache, vomiting, and papilledema.
Which combination of clinical findings is most indicative of bone marrow failure in a child with leukemia?
A. Fever, anorexia, and hepatosplenomegaly
B. Lymphadenopathy, headache, and papilledema
C. Enlarged testicle, pallor, and vomiting
D. Petechiae, frank bleeding, and joint pain
D. Petechiae, frank bleeding, and joint pain
Rationale: Petechiae, frank bleeding, and joint pain are hallmark signs of bone marrow failure in leukemia, caused by reduced production of platelets, erythrocytes, and normal white blood cells.
Which diagnostic test is definitive for confirming leukemia?
A. Complete blood count (CBC)
B. Bone marrow aspiration
C. Serum uric acid level
D. Flow cytometric assay
B. Bone marrow aspiration
Rationale: Bone marrow aspiration reveals immature and abnormal lymphoblasts and hypercellular marrow, making it the definitive diagnostic test for leukemia.
A 5-year-old child is diagnosed with ALL. The initial blood work shows anemia, thrombocytopenia, and neutropenia. What phase of chemotherapy is focused on achieving maximum cell death and remission?
A. Consolidation
B. Induction
C. Delayed intensification
D. Maintenance
B. Induction
Rationale: The induction phase is aimed at achieving maximum cell death to induce remission.
A child with ALL is undergoing the consolidation phase of treatment. Which medication is typically administered during this phase?
A. L-asparaginase
B. Vincristine
C. Methotrexate
D. Doxorubicin
A. L-asparaginase
Rationale: L-asparaginase is commonly administered during the consolidation phase to target leukemic cells.
What is the significance of a leukocyte count above 50,000 at the time of diagnosis in children with leukemia?
A. It is indicative of a better prognosis.
B. It increases the likelihood of CNS involvement.
C. It correlates with a worse prognosis.
D. It requires immediate HSCT.
C. It correlates with a worse prognosis.
Rationale: A higher leukocyte count at diagnosis is associated with a worse prognosis.
A 7-year-old child with AML relapses one year after completing treatment. What treatment option would most likely be recommended next?
A. Maintenance chemotherapy
B. Cranial irradiation
C. Hematopoietic stem cell transplant (HSCT)
D. L-asparaginase therapy
C. Hematopoietic stem cell transplant (HSCT)
Rationale: HSCT is recommended for children who relapse and achieve a second remission in ALL or for AML, even if remission has not been achieved.
During which phase of chemotherapy for ALL are additional drugs introduced to target surviving leukemic cells?
A. Maintenance
B. Consolidation
C. Delayed intensification
D. Induction
C. Delayed intensification
Rationale: The delayed intensification phase introduces additional drugs to target leukemic cells that have survived earlier treatments.
A 6-year-old child undergoing treatment for ALL presents with elevated serum uric acid, hypocalcemia, and hyperphosphatemia. What condition should the nurse monitor for based on these lab findings?
A. Tumor lysis syndrome
B. CNS infiltration
C. Anemia
D. Thrombocytopenia
A. Tumor lysis syndrome
Rationale: Elevated uric acid, hypocalcemia, and hyperphosphatemia are hallmark findings of tumor lysis syndrome, which can occur during leukemia treatment.
Which factor has the most significant impact on the prognosis of a child with leukemia?
A. FAB classification type
B. Age at diagnosis
C. Presence of hepatosplenomegaly
D. Initial leukocyte count
D. Initial leukocyte count
Rationale: The initial leukocyte count is a critical prognostic factor, with higher counts being associated with worse outcomes.
A 10-year-old with ALL has CNS involvement. What treatment is most appropriate to address this complication?
A. L-asparaginase
B. Cranial irradiation and intrathecal chemotherapy
C. Hematopoietic stem cell transplant
D. Vincristine and prednisone
B. Cranial irradiation and intrathecal chemotherapy
Rationale: CNS involvement in leukemia is treated with cranial irradiation and intrathecal chemotherapy to target leukemic cells in the CNS.
What is the primary goal of the maintenance phase of chemotherapy in ALL treatment?
A. Reduce CNS involvement
B. Destroy remaining leukemic cells
C. Induce remission
D. Prevent anemia and thrombocytopenia
B. Destroy remaining leukemic cells
Rationale: The maintenance phase focuses on destroying any remaining leukemic cells to prevent relapse.
A child with ALL is being monitored for minimal residual disease (MRD). What laboratory test is most effective for identifying very small numbers of leukemic cells?
A. Bone marrow aspiration
B. Rapid flow cytometric assay
C. Complete blood count (CBC)
D. Serum uric acid level
B. Rapid flow cytometric assay
Rationale: Rapid flow cytometric assay is a sensitive test for detecting minimal residual disease, improving treatment outcomes.