1995
DOI: 10.1016/0003-4975(95)00782-2
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De novo solid malignancies after cardiac transplantation

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Cited by 63 publications
(54 citation statements)
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“…This has been reported in renal, 1 bone marrow, 2 heart, 3 and liver [4][5][6][7][8] transplant recipients and is related to an increased number of nonmelanoma skin cancers 9 and lymphomas. 5,6 Although immunosuppression has a central role in the development of cancer, the risk for de novo tumor after orthotopic liver transplantation (OLT) has not been well studied.…”
mentioning
confidence: 98%
“…This has been reported in renal, 1 bone marrow, 2 heart, 3 and liver [4][5][6][7][8] transplant recipients and is related to an increased number of nonmelanoma skin cancers 9 and lymphomas. 5,6 Although immunosuppression has a central role in the development of cancer, the risk for de novo tumor after orthotopic liver transplantation (OLT) has not been well studied.…”
mentioning
confidence: 98%
“…13 For heart transplant recipients, the mean age of diagnosis is 43 to 47 years; which is still younger than those with classic Kaposi sarcoma. 8,14 Also, the log time of developing cancer after transplant is shorter, with a mean of 12 to 14 months. 13,14 Infection with human herpesvirus 8 has been established as the cause of this cancer, and immunosuppression plays a key role in this context.…”
Section: Kaposi Sarcomamentioning
confidence: 99%
“…8,14 Also, the log time of developing cancer after transplant is shorter, with a mean of 12 to 14 months. 13,14 Infection with human herpesvirus 8 has been established as the cause of this cancer, and immunosuppression plays a key role in this context. 8 Penn found that 60% of Kaposi sarcoma cases were nonvisceral (98% skin lesions, 2% mouth or oropharyngeal), with the remaining 40% being visceral, mainly involving the gastrointestinal tract, lungs, and lymph nodes.…”
Section: Kaposi Sarcomamentioning
confidence: 99%
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