Foetal loss and infant deaths in families of children with soft-tissue sarcoma
✍ Scribed by Ann L. Hartley; Jillian M. Birch; Valerie Blair; Anna M. Kelsey; Patricia H. Morris Jones
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- French
- Weight
- 479 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Distribution of miscarriages, stillbirths and infant deaths in the families of a population‐based series of children with soft‐tissue sarcoma was examined in relation to index case histology (rhabdomyosarcoma or other soft‐tissue sarcoma) and to the possible presence of genetic predisposition to cancer in the families (Li‐Fraumeni syndrome or neurofibromatosis). Reproductive loss was not related to index histology (miscarriages, p = 0.3; all losses, p = 0.6) but was significantly higher in “genetic” rather than “sporadic” families (miscarriages, p = 0.02; all losses, p = 0.01). However, excess reproductive loss was not a feature of families with the Li‐Fraumeni syndrome, but appeared to be concentrated in the families affected by neurofibromatosis.
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This article presents analysis of clinical and family data for 239 patients with childhood soft tissue sarcoma (STS) treated at the Institut Gustave Roussy in Villejuif. ## METHODS. A molecular study was performed to detect germline p53 mutations in the 44 families in which at least 1 relative de
## Abstract ## BACKGROUND Patients affected by neurofibromatosis type 1 (NF1) are at higher risk of developing soft‐tissue sarcomas (STS) than the general population. The clinical findings and outcome in 43 children and adolescents with NF1 treated for STS in the Italian protocols between 1988 and