Liposarcoma risk factors: Difference between revisions
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Line 13: | Line 13: | ||
**Chlorophenols | **Chlorophenols | ||
**Dioxin contaminations | **Dioxin contaminations | ||
**Arsenic | |||
**Thorium dioxide([[Thorotrast]]) | |||
*Radiation | *Radiation | ||
Line 21: | Line 23: | ||
*Genetic susceptibility | *Genetic susceptibility | ||
**[[Li-Fraumeni syndrome]] | **[[Li-Fraumeni syndrome]] | ||
**[[Neurofibromatosis]] (NF1; von Recklinghausen disease) | |||
**[[Gardner syndrome]] (Familial adenomatous polyposis) | |||
**[[Retinoblastoma]] | |||
**[[Werner syndrome]] | |||
**Nevoid [[basal cell carcinoma]] (Gorlin syndrome) | |||
*[[Viral infection]] | *[[Viral infection]] |
Revision as of 14:43, 25 August 2015
Liposarcoma Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Risk factors of liposarcoma includes chemical carcinogens, genetic disorders, radiation and immunodeficiency. These increases the risk of liposarcoma in general population.
Risk factors
Liposarcoma is associated with a number of risk factors. Few of them are listed below.
- Chemical carcinogens
- Phenoxyacetic herbicides
- Chlorophenols
- Dioxin contaminations
- Arsenic
- Thorium dioxide(Thorotrast)
- Radiation
- Immunodeficiency
- Regional acquired immunodeficiency is sometimes associated with liposarcoma
- Genetic susceptibility
- Li-Fraumeni syndrome
- Neurofibromatosis (NF1; von Recklinghausen disease)
- Gardner syndrome (Familial adenomatous polyposis)
- Retinoblastoma
- Werner syndrome
- Nevoid basal cell carcinoma (Gorlin syndrome)