Familial neural crest tumours
- 1 September 1991
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 150 (11) , 789-792
- https://doi.org/10.1007/bf02026713
Abstract
It is known that some cases of neural crest tumours are hereditary. We report the clinical and cytogenetic findings in a three-generation, extended family, four members of which developed single or multiple neural crest tumours (ganglioneuroma, ganglioneuroblastoma or neuroblastoma). To our knowledge, this is the first report of a family with three generations affected. No constitutional cytogenetic abnormality was found in the two members tested. We also review the literature on familial neural crest tumours, with emphasis on those affecting more than one generation. It is important that a detailed family history, with particular reference to tumours, is obtained in all cases of childhood cancer.Keywords
This publication has 26 references indexed in Scilit:
- Familial Occurrence of Neuroblastoma, Von Recklinghausen's Neurofibromatosis, Hirschsprung's Agangliosis and Jaw‐winking SyndromeActa Paediatrica, 1989
- Improvements in survival from childhood cancer: results of a population based survey over 30 yearsBMJ, 1988
- Biological characterization and clinical applications of a monoclonal antibody recognizing an antigen restricted to neuroectodermal tissuesInternational Journal of Cancer, 1983
- Neuroblastoma in a pair of identical twinsMedical and Pediatric Oncology, 1982
- Multifocal nondisseminated neuroblastomaThe Journal of Pediatrics, 1978
- Familial neuroblastomaThe Journal of Pediatrics, 1975
- Familia neuroblastoma: report of two sib pairs.Archives of Disease in Childhood, 1973
- Familial neuroblastoma: Report of a kindred with a high incidence of infantile tumorsThe Journal of Pediatrics, 1972
- FAMILIAL NEUROBLASTOMA AND TRISOMY 13Archives of Pediatrics & Adolescent Medicine, 1971
- Familial NeuroblastomaArchives of Pediatrics & Adolescent Medicine, 1971