Adult T-cell leukemia epidemiology and demographics: Difference between revisions
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==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
===Prevalence=== | ===Prevalence=== | ||
* In the US, adult T-cell leukemia is considered a rare disease that mainly tends to affect African American intravenous drug abusers. | |||
===Incidence=== | ===Incidence=== | ||
Revision as of 15:35, 24 January 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Haytham Allaham, M.D. [2]
Overview
Epidemiology and Demographics
Prevalence
- In the US, adult T-cell leukemia is considered a rare disease that mainly tends to affect African American intravenous drug abusers.
Incidence
Age
- The incidence of adult T-cell leukemia increases with age; the median age at diagnosis is 57 years.
- The age of onset for adult T-cell leukemia differs across geographical regions, such as:
- The median age at diagnosis in Japan is 60 years
- The median age at diagnosis in Central America is 40 years
Gender
- Females are more commonly affected with adult T-cell leukemia than males. The female to male ratio is approximately 1.4 to 1.
- Females are more commonly affected with HTLV infection than males.
- However, the risk of adult T-cell leukemia development among HTLV male carriers is five fold higher than the risk of adult T-cell leukemia development among HTLV female carriers.
Race
- The majority of adult T-cell leukemia cases are mainly reported in Japan, the Caribbean, South America, and Africa.
- Adult T-cell leukemia usually affects individuals of the African American race. Caucasian individuals are less likely to develop adult T-cell leukemia.