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Oncology
Chronic Lymphocytic Leukemia: Review Questions
Eric Jacobsen, MD, and David C. Fisher, MD
Dr. Jacobsen is a hematologic malignancies fellow and Dr. Fisher is an instructor in medicine; both are at the Dana-Farger Cancer Institute and Harvard Medical School, Boston, MA.
Choose the single best answer for each question.
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1. A 75-year-old woman is referred from her primary care physician with a leukocyte count of 34× 103/mm3 with 80% lymphocytes, hemoglobin concentration of 13 g/dL, hematocrit of 40%, and platelet count of 220× 103/mm3. A physical examination and computed tomography (CT) scan show no evidence of lymphadenopathy, splenomegaly, or hepatomegaly. She is asymptomatic. What is the most appropriate treatment for this patient at this time?
- Bone marrow transplantation
- Chlorambucil
- Chlorambucil and fludarabine in combination
- Hydroxyurea to eliminate the risk of leukostasis
- No treatment is indicated at this time
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2. A 57-year-old man with a history of untreated stage I chronic lymphocytic leukemia (CLL) presents to the emergency department (ED) with a 1-week history of fatigue. He denies any trauma, melena, or hematemesis. His hematocrit is 14%, with a platelet count of 175 × 103/mm3 and leukocyte count of
22 × 103/mm3 with 68% lymphocytes. His chemistry profile is normal except for an elevated indirect bilirubin. A peripheral blood smear shows numerous spherocytes. His physical examination is unremarkable except for pallor. His most recent complete blood count (2 weeks earlier) revealed a hematocrit of 38%, a leukocyte count of 19 ×103/mm3 with 70% lymphocytes, and a platelet count of 190 × 103/mm3. What is this patients most likely diagnosis?
- Close follow-up with mammography, chest radiography, complete blood count, and tumor marker analysis every 6 months
- Autoimmune hemolytic anemia
- Progression to stage IV CLL with subsequent anemia from bone marrow replacement
- Pure erythrocyte aplasia
- Splenomegaly with splenic sequestration of erythrocytes
- Thrombotic thrombocytopenic purpura
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3. A 65-year-old man has stage IV CLL, which was previously treated. Most recently, he was treated with alemtuzumab. One month after receiving alemtuzumab, he presents to the ED with a 1-week history of nonproductive cough, low-grade fevers, and progressive shortness of breath without prodromal symptoms. He lives in New Hampshire and has not traveled recently. He is tachypneic with an oxygen saturation of 85% on room air, hemodynamically stable, and has a temperature of 101.8°F. A chest radiograph shows a faint bilateral interstitial infiltrate. What is this patientıs most likely diagnosis?
- Histoplasmosis
- Hypersensitivity pneumonitis from alemtuzumab
- Pneumocystis carinii pneumonia
- Pneumococcal pneumonia
- Pulmonary infiltration with CLL
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4. A 56-year-old woman has stage I CLL characterized by cervical and axillary lymphadenopathy. She has never been treated. She presents to clinic complaining of a 2-week history of worsening fatigue but no other symptoms. On physical examination, a markedly enlarged right cervical lymph node is noted, while the remainder of her lymph nodes are unchanged from a previous examination. The oropharynx is slightly red, but the tonsils are normal and without exudate. Which of the following is the most appropriate diagnostic test?
- Cervical lymph node biopsy
- CT of the neck
- Laryngoscopy
- Monospot
- Rapid test for streptococci
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