Abstract
Transgender and gender diverse (TGD) populations with hereditary cancer syndromes face unique obstacles to identifying and obtaining appropriate cancer surveillance and risk-reducing procedures. There is a lack of care provider knowledge about TGD health management. Lynch syndrome (LS) is one of the most common hereditary cancer syndromes, affecting an estimated 1 in 279 individuals. There are no clinical guidelines specific for TGD individuals with LS, highlighting a need to improve the quality of care for this population. There is an urgent need for cancer surveillance recommendations for TGD patients. This commentary provides recommendations for cancer surveillance, risk-reducing strategies, and genetic counseling considerations for TGD patients with LS.
Original language | English (US) |
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Pages (from-to) | 437-448 |
Number of pages | 12 |
Journal | Familial Cancer |
Volume | 22 |
Issue number | 4 |
DOIs | |
State | Published - Oct 2023 |
Keywords
- Cancer
- Lynch syndrome
- Management
- Surveillance
- Transgender and gender diverse
ASJC Scopus subject areas
- Genetics(clinical)
- Genetics
- Oncology
- Cancer Research