RESUMO
In patients successfully treated for hereditary retinoblastoma, the risk of developing a second non-ocular tumor has been reported. We report the first case of primary hepatic leiomyosarcoma in a 39 year-old woman who has been treated 37 years before for hereditary retinoblastoma of the left eye. The patient presented with right upper quadrant abdominal pain and fever. Histological diagnosis was made by liver biopsy. As surgical resection was impossible, chemotherapy with epirubicin, then ifosfamide, etoposide and cisplatin was performed. The patient died 22 months after diagnosis. Genetic abnormalities observed in hereditary retinoblastoma, which probably resulted in a predisposition to the development of hepatic cancer in this patient, were not investigated.
Assuntos
Neoplasias Oculares/genética , Leiomioma Epitelioide , Neoplasias Hepáticas , Segunda Neoplasia Primária , Retinoblastoma/genética , Adulto , Neoplasias Oculares/cirurgia , Feminino , Humanos , Leiomioma Epitelioide/terapia , Neoplasias Hepáticas/terapia , Segunda Neoplasia Primária/terapia , Retinoblastoma/cirurgia , Fatores de TempoRESUMO
No epidemiological data on the incidence of duodenal ulcer are available for a well-defined population in France. We therefore conducted a prospective study in the urban population of Reims. All radiologists, gastroenterologists and surgeons of this town were asked to report all new cases of duodenal ulcer seen during one year. During 1988, 114 new cases were identified. Age standardized incidence using world population standards were 83.6/100,000 for males and 29.5/100,000 for females. The male/female ratio was 2.8. Mean age at the time of diagnosis was 51.9 years, higher for females (63.4 years) than for males (48.0 years). Nearly one third (32.5%) of duodenal ulcers presented with complications (haemorrhage or perforation) at the time of initial diagnosis.