Cutaneous Malignant Melanoma in Survivors of Heritable Retinoblastoma
- 1 August 1988
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 106 (8) , 1059-1061
- https://doi.org/10.1001/archopht.1988.01060140215026
Abstract
• Six survivors of bilateral retinoblastoma developed cutaneous malignant melanoma 20 to 51 years (average, 31 years) after initial therapy for the ocular tumor. Five patients received radiation therapy to the orbital area. In two patients the cutaneous malignant melanoma developed in the field of irradiation. Two patients developed multiple cutaneous melanomas and are thought to have the dysplastic nevus syndrome. At this writing two patients are alive and well after wide resection of their skin tumors. A review of the literature suggests that cutaneous malignant melanoma accounts for about 7% of second malignant neoplasms in survivors of heritable retinoblastoma.This publication has 26 references indexed in Scilit:
- Second primary neoplasms in patients with retinoblastomaBritish Journal of Cancer, 1986
- Second Nonocular Tumors in Survivors of Heritable RetinoblastomaArchives of Ophthalmology (1950), 1986
- Acute non-lymphocytic leukemia following multimodality therapy for retinoblastomaCancer, 1985
- Osteogenic Sarcoma of the Humerus after Cobalt Plaque Treatment for RetinoblastomaAmerican Journal of Ophthalmology, 1980
- Retinoblastoma: a study of natural history and prognosis of 268 cases.BMJ, 1975
- Retinoblastoma: Epidemiologic CharacteristicsNew England Journal of Medicine, 1971
- SECOND PRIMARY NEOPLASMS IN CHILDRENAmerican Journal of Roentgenology, 1968
- Radiation-induced neoplasms following curative therapy for retinoblastomaCancer, 1966
- SARCOMA FOLLOWING RADIATION FOR RETINOBLASTOMAActa Ophthalmologica, 1965
- Osteogenic Sarcoma following Irradiation for Retinoblastoma*American Journal of Ophthalmology, 1952