## Abstract ## BACKGROUND Patients with chronic lymphocytic leukemia (CLL) that transforms to Richter syndrome (RS) frequently show atypical lymphocytes in bone marrow; however, a diagnosis of RS requires confirmation of the presence of sheets of large cells in bone marrow or lymph nodes. ## METH
Chronic lymphocytic leukemia: Changes in bone marrow composition and distribution assessed with quantitative MRI
β Scribed by Frederic E. Lecouvet; Bruno C. Vande Berg; Lucienne Michaux; Jean-Marie Scheiff; Jacques Malghem; Jacques Jamart; Baudouin E. Maldague; Jean Louis Michaux; Augustin Ferrant
- Book ID
- 102906546
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 829 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1053-1807
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β¦ Synopsis
Abstract
The purposes of this study were (Ξ±) to determine the prevalence of bone marrow abnormalities in patients with chronic lymphocytic leukemia (CLL) using quantitative MR assessment of axial marrow composition and peripheral marrow distribution; (b) to assess the agreement between both quantitative MR methods and compare their sensitivities to detect marrow alterations; and (c) to correlate MR findings with clinical and laboratory parameters. Twentyβnine consecutive patients with biopsyβproven CLL were investigated on a .5βT MR imager to determine bulk T1 relaxation times of the vertebral bone marrow and proportion of proximal femur surface area occupied by nonfatty marrow on coronal T1βweighted MR images of one hip. Of the 29 patients, 12 (41%) had abnormal increase in lumbar marrow T1 values (>600 msec) and 16 (55%) had increased proportion of surface area occupied by nonβfatty marrow in the proximal femur (>+1 SD compared to normal values determined in sexβ and ageβmatched healthy subjects). The results of both quantitative MR methods were normal in 12 patients and abnormal in 11 patients (agreement, 79%). Patients with alterations in peripheral marrow distribution had significantly higher T1 relaxation times (P = .001) than those with normal peripheral marrow. Patients with abnormal marrow composition or distribution at MRI had significantly higher blood and marrow lymphocytosis than patients without these features. In conclusion, the agreement between both quantitative MR methods suggests a parallelism between changes in axial marrow composition and in peripheral marrow distribution in patients with CLL. The limits of quantitative MRI in CLL must be kept in mind, because quantitative MR methods failed to detect leukemic marrow infiltration in 41% of patients.
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