T-cell prolymphocytic leukemia overview: Difference between revisions
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==Overview== | ==Overview== | ||
T-cell-prolymphocytic leukemia (T-PLL) is a mature [[T-cell]] [[leukemia]] with aggressive behavior and predilection for [[blood]], [[bone marrow]], [[lymph nodes]], [[liver]], [[spleen]], and [[skin]] involvement.<ref name="who1"> Jaffe E.S., Harris N.L., Stein H., Vardiman J.W. (eds): [http://www.iarc.fr/WHO-BlueBooks/BBwebsite/bb3.html World Health Organization Classification of Tumors]. Pathology and Genetics of Tumours of Haemopoietic and Lymphoid Tissues. IARC Press: Lyon 2001</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 16:06, 20 August 2015
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T-cell prolymphocytic leukemia Microchapters |
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Differentiating T-cell Prolymphocytic Leukemia from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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T-cell prolymphocytic leukemia overview On the Web |
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American Roentgen Ray Society Images of T-cell prolymphocytic leukemia overview |
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Directions to Hospitals Treating T-cell prolymphocytic leukemia |
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Risk calculators and risk factors for T-cell prolymphocytic leukemia overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
T-cell-prolymphocytic leukemia (T-PLL) is a mature T-cell leukemia with aggressive behavior and predilection for blood, bone marrow, lymph nodes, liver, spleen, and skin involvement.[1]
References
- ↑ Jaffe E.S., Harris N.L., Stein H., Vardiman J.W. (eds): World Health Organization Classification of Tumors. Pathology and Genetics of Tumours of Haemopoietic and Lymphoid Tissues. IARC Press: Lyon 2001