Exam 25: Myelodysplastic Syndromes
Exam 1: Introduction30 Questions
Exam 2: Cellular Homeostasis40 Questions
Exam 3: Structure and Function of Hematopoietic Organs35 Questions
Exam 4: Hematopoiesis35 Questions
Exam 5: The Erythrocyte37 Questions
Exam 6: Hemoglobin40 Questions
Exam 7: Granulocytes and Monocytes30 Questions
Exam 8: Lymphocytes25 Questions
Exam 9: The Platelet16 Questions
Exam 10: The Complete Blood Count and Peripheral Blood Smear Evaluation35 Questions
Exam 11: Introduction to Anemia35 Questions
Exam 12: Anemias of Disordered Iron Metabolism and Heme Synthesis36 Questions
Exam 13: Hemoglobinopathies: Qualitative Defects33 Questions
Exam 14: Thalassemia32 Questions
Exam 15: Megaloblastic and Nonmegaloblastic Macrocytic Anemias34 Questions
Exam 16: Hypoproliferative Anemias32 Questions
Exam 17: Hemolytic Anemia: Membrane Defects36 Questions
Exam 18: Hemolytic Anemia: Enzyme Deficiencies36 Questions
Exam 19: Hemolytic Anemia: Immune Anemias30 Questions
Exam 20: Hemolytic Anemia: Nonimmune Defects30 Questions
Exam 21: Nonmalignant Disorders of Leukocytes: Granulocytes and Monocytes35 Questions
Exam 22: Nonmalignant Lymphocyte Disorders32 Questions
Exam 23: Introduction to Hematopoietic Neoplasms34 Questions
Exam 24: Myeloproliferative Neoplasms44 Questions
Exam 25: Myelodysplastic Syndromes34 Questions
Exam 26: Acute Myeloid Leukemias35 Questions
Exam 27: Precursor Lymphoid Neoplasms34 Questions
Exam 28: Mature Lymphoid Neoplasms39 Questions
Exam 29: Hematopoietic Stem Cell Transplantation41 Questions
Exam 30: Morphologic Analysis of Body Fluids in the Hematology Laboratory39 Questions
Exam 31: Primary Hemostasis35 Questions
Exam 32: Secondary Hemostasis and Fibrinolysis33 Questions
Exam 33: Disorders of Primary Hemostasis35 Questions
Exam 34: Disorders of Secondary Hemostasis34 Questions
Exam 35: Thrombophilia34 Questions
Exam 36: Hemostasis: Laboratory Testing and Instrumentation41 Questions
Exam 37: Hematology Procedures46 Questions
Exam 38: Bone Marrow Examination34 Questions
Exam 39: Automation in Hematology38 Questions
Exam 40: Flow Cytometry34 Questions
Exam 41: Chromosome Analysis of Hematopoietic and Lymphoid Disorders35 Questions
Exam 42: Molecular Analysis of Hematologic Diseases18 Questions
Select questions type
Which of the World Health Organization's MDS subgroups contains two or more cytopenias,rare or no blasts,<1 × 10⁹/L monocytes in the peripheral blood,<5% blasts,and <15% ringed sideroblasts in the bone marrow?
Free
(Multiple Choice)
4.9/5
(69)
Correct Answer:
C
Which of the following characteristics are associated with a poor prognosis for MDS?
Free
(Multiple Choice)
4.9/5
(85)
Correct Answer:
A
Explain the relationship between myelodysplastic syndromes and acute leukemia.
Free
(Essay)
4.8/5
(88)
Correct Answer:
Myelodysplastic syndromes eventually can progress into acute leukemia.Acute leukemia as defined by the WHO is classified with >20% blasts in the bone marrow.The MDS family is classified as <20% blasts proliferating in the marrow.
Which test or tests support the theory that the abnormal cells in MDS are clones derived from an abnormal pluripotent stem cell?
(Multiple Choice)
4.9/5
(72)
All of the following are considered morphologic evidence of dyserythropoiesis except:
(Multiple Choice)
5.0/5
(76)
The chromosomal abnormalities present in most cases of MDS are located on which of the following chromosomes?
(Multiple Choice)
4.8/5
(81)
What is the major criterion for the diagnosis of acute leukemia?
(Multiple Choice)
4.8/5
(98)
Myelodysplastic syndromes are sometimes called preleukemias because:
(Multiple Choice)
4.8/5
(89)
Which of the following represents the granule pattern of a dysplastic cell in MDS?
(Multiple Choice)
4.7/5
(73)
Which of the following does the World Health Organization's classification consider an MDS/MPN variant?
(Multiple Choice)
4.8/5
(73)
A 60-year-old patient visited his general practitioner because of fatigue and unexplained bruising.Physical examination revealed a frail,thin,pale man with widespread bruising.A CBC was ordered and revealed abnormal granularity of platelets and leukocytes.Red cells appeared dimorphic.Bone marrow analysis showed 20% ringed sideroblasts with dysplastic changes in RBC and WBC precursors.No cytogenetic abnormalities were detected.Based on this information,what is a probable diagnosis?
(Multiple Choice)
4.8/5
(86)
A technologist is reviewing a blood smear and finds a rare blast.Bone marrow analysis shows dysplasia in 30% of the erythroblasts and the myeloid precursors and 4% blasts.What is a possible diagnosis based on these findings?
(Multiple Choice)
4.9/5
(83)
Which of the following is a defining characteristic of myelodysplastic syndromes (MDS)?
(Multiple Choice)
4.9/5
(59)
A 61-year-old woman saw her primary care physician because of fatigue and dyspnea on exertion for the past 3 months.Past medical history noted that the patient had been treated 5 years earlier with the DNA alkylating agent cyclophosphamide,non-Hodgkin lymphoma.A CBC revealed the following:
WBC: 3.6* 10⁹/L
RBC: 2.8 * 10₁₂ /L
Hb: 9.1 g/dL
MCV: 104 fL
Reticulocyte count: 2.0%
Normal vitamin B₁₂ and folic acid levels
PLT: 120 * 10⁹/L
Differential: 6% blasts
A bone marrow biopsy revealed hypercellularity,and dyshematopoiesis of all three myeloid lineages.
Suggest an appropriate follow-up test and a likely diagnosis for this patient.
(Essay)
4.8/5
(74)
According to the WHO classification,what percent of blasts must be present in the bone marrow to classify a patient with acute leukemia?
(Multiple Choice)
4.9/5
(78)
A bone marrow specimen is received in the cytogenetics lab.FISH analysis has been ordered.The laboratician performs the assay and notices that 96% of the patient's cells contain both 5q- and 12q- deletions.These cytogenetic findings are characteristic of:
(Multiple Choice)
4.9/5
(89)
An unknown cell possesses the following characteristics: blastlike with open chromatin pattern,prominent nucleoli,absence of granules,and a high N:C ratio.Based on this information,what is the cell's most probable identity?
(Multiple Choice)
4.8/5
(90)
All of the following are included in the MDS/MPN family except:
(Multiple Choice)
5.0/5
(83)
Which World Health Organization (WHO)classification for MDS is best supported when the peripheral blood shows a general cytopenia,5-19% blasts with Auer rods,and <1 × 10⁹ /L monocytes?
(Multiple Choice)
4.8/5
(76)
Showing 1 - 20 of 34
Filters
- Essay(0)
- Multiple Choice(0)
- Short Answer(0)
- True False(0)
- Matching(0)