T-cell prolymphocytic leukemia epidemiology and demographics: Difference between revisions
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==Overview== | ==Overview== | ||
T-cell prolymphocytic leukemia is a rare condition. Its incidence increases with age. with ataxia telangiectasia, the median age at diagnosis is 30 years. | |||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
*T-cell prolymphocytic leukemia is very rare, and it represents 2% of all small lymphocytic leukemias in adults. | *T-cell prolymphocytic leukemia is very rare, and it represents 2% of all small lymphocytic leukemias in adults. | ||
Revision as of 18:13, 28 March 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Qurrat-ul-ain Abid, M.D.[2], Maria Fernanda Villarreal, M.D. [3]
Overview
T-cell prolymphocytic leukemia is a rare condition. Its incidence increases with age. with ataxia telangiectasia, the median age at diagnosis is 30 years.
Epidemiology and Demographics
- T-cell prolymphocytic leukemia is very rare, and it represents 2% of all small lymphocytic leukemias in adults.
- The incidence of T-cell prolymphocytic leukemia increases with age; the median age at diagnosis is 65 years.[1]
- Patients with ataxia telangiectasia and T-cell prolymphocytic leukemia are young adults; the median age at diagnosis is 30 years.
- Males are slightly more affected with T-cell prolymphocytic leukemia than females.
- There is no racial predilection for T-cell prolymphocytic leukemia.
- T-PLL is a rare leukemia, primarily affecting adults over the age of 30. It represents 2% of all small lymphocytic leukemias in adults.[2]
References
- ↑ Graham RL, Cooper B, Krause JR (2013). "T-cell prolymphocytic leukemia". Proc (Bayl Univ Med Cent). 26 (1): 19–21. PMC 3523759. PMID 23382603.
- ↑ Matutes E, Brito-Babapulle V, Swansbury J; et al. (1991). "Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia". Blood. 78 (12): 3269–74. PMID 1742486.