Oncologic manifestations of neurofibromatosis type 1 in Korea / 대한외과학회지
Journal of the Korean Surgical Society
; : 205-210, 2012.
Article
en En
| WPRIM
| ID: wpr-15812
Biblioteca responsable:
WPRO
ABSTRACT
PURPOSE: The aim of this study was to investigate the incidence and spectrum of malignant tumors in Korean neurofibromatosis type 1 (NF1) patients. METHODS: We retrospectively reviewed 125 patients who were diagnosed with NF1 at a single institution from 1995 to 2010. The incidence, location, histologic type, and radiologic findings of malignant tumors as well as development of multiple primary tumors were analyzed. RESULTS: Eighteen malignant tumors occurred in 16 patients (12.8%) among 125 Korean NF1 patients; 9 carcinomas, 8 sarcomas and 1 central nervous system (CNS) tumor. Five tumors were of nervous system origin and 13 were non-nervous system tumors. The locations of the tumors were as follow: 1 CNS, 2 lung, 3 breast, 3 stomach, 3 small bowel, 1 colon, 1 liver, 1 uterus, 1 neck, and 2 in extremities. Three malignant peripheral nerve sheath tumors (MPNSTs) occurred at the neck and extremity, and one in the liver. All three gastrointestinal stromal tumors (GISTs) had multiple tumors in the jejunum, and one MPNST and one pheochromocytoma were accompanied in two GISTs. Multiple primary tumors, benign or malignant were reported in 4 patients (25.0%), synchronously or metachronously. CONCLUSION: Korean NF1 patients had a high risk of developing malignant tumors. The common malignant tumors in Koreans such as breast, lung and stomach cancers developed frequently in addition to the NF1-related tumors such as MPNST or GIST.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Feocromocitoma
/
Sarcoma
/
Estómago
/
Neoplasias Gástricas
/
Útero
/
Mama
/
Sistema Nervioso Central
/
Incidencia
/
Estudios Retrospectivos
/
Neurofibromatosis 1
Tipo de estudio:
Incidence_studies
/
Observational_studies
/
Prognostic_studies
Límite:
Humans
País/Región como asunto:
Asia
Idioma:
En
Revista:
Journal of the Korean Surgical Society
Año:
2012
Tipo del documento:
Article