Unusually indolent T‐cell prolymphocytic leukemia associated with a complex karyotype: Is this T‐cell chronic lymphocytic leukemia?
T‐cell prolymphocytic leukemia (T‐PLL) is typically associated with an aggressive clinical course, with a median survival of less than 1 year. We report a case of T‐PLL that displays multiple cytogenetic abnormalities, with the most complex subclone having the following karyotype: 47, Y, −X, +8, inv...
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Published in: | American journal of hematology Vol. 71; no. 3; pp. 224 - 226 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
New York
Wiley Subscription Services, Inc., A Wiley Company
01-11-2002
Wiley-Liss |
Subjects: | |
Online Access: | Get full text |
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Summary: | T‐cell prolymphocytic leukemia (T‐PLL) is typically associated with an aggressive clinical course, with a median survival of less than 1 year. We report a case of T‐PLL that displays multiple cytogenetic abnormalities, with the most complex subclone having the following karyotype: 47, Y, −X, +8, inv (10) (p12q26), del (11) (p13p15) +marker. However, despite this genetic complexity, the leukemia has behaved in a remarkably indolent manner, with the patient remaining asymptomatic, without therapeutic intervention, for more than 7 years. The unusually benign behavior of this disease calls into question the validity of grouping such cases under the umbrella of T‐PLL and warrants a reconsideration of T‐cell chronic lymphocytic leukemia (no longer recognized as a distinct disease) as a bona fide diagnostic entity. Am. J. Hematol. 71:224–226, 2002. © 2002 Wiley‐Liss, Inc. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 0361-8609 1096-8652 |
DOI: | 10.1002/ajh.10221 |