Abstract
Telomere biology disorders predispose affected individuals to specific malignancies and organ fibrosis in tissues sensitive to telomere length (TL) shortening, especially after exposure to chemotherapy and radiation. We report a case of a 17-year-old female with Hodgkin lymphoma who developed severe chemotherapy-related toxicities. She was subsequently found to have peripheral blood lymphocyte TL < 1st percentile and a pathogenic variant in TERT inherited from her father. This case demonstrates that early genetic evaluation of patients who experience greater than expected therapy-related toxicities may be warranted to help guide further decisions regarding therapy, imaging modalities, and lifelong cancer prevention surveillance.
Original language | English (US) |
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Article number | e27779 |
Journal | Pediatric Blood and Cancer |
Volume | 66 |
Issue number | 8 |
DOIs | |
State | Published - Aug 2019 |
Keywords
- Hodgkin disease
- MDS
- late effects of cancer treatment
- lymphoma
- molecular genetics
- telomerase
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Hematology
- Oncology