Myeloid leukemia in Prader-Willi syndrome

被引:40
作者
Davies, HD
Leusink, GL
McConnell, A
Deyell, M
Cassidy, SB
Rick, GH
Coppes, MJ
机构
[1] Univ Calgary, Dept Pediat, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Dept Oncol, Calgary, AB T2N 1N4, Canada
[3] Alberta Childrens Prov Gen Hosp, Childrens Canc Program, Calgary, AB T2T 5C7, Canada
[4] Tom Baker Canc Clin, Dept Community Hlth Sci, Calgary, AB, Canada
[5] Univ Calif Irvine, Dept Genet, Irvine, CA 92717 USA
[6] Alberta Childrens Prov Gen Hosp, Child Hlth Res Unit, Calgary, AB T2T 5C7, Canada
[7] Tom Baker Canc Clin, Dept Pediat, Calgary, AB, Canada
关键词
D O I
10.1067/mpd.2003.81
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To evaluate the frequency of cancers recorded by the Surveillance, Epidemiology, and End Results (SEER) Program in persons with Prader-Willi syndrome (PWS) Methods A survey was mailed in 1994 to 1852 registrants of the PWS Association (USA) inquiring about a diagnosis of any type of benign tumor or cancer (malignant tumor or leukemia). The risk of developing cancer was then estimated by comparing the observed number of cancers in the PWS population during 1975 to 1994 to the expected number in the general US population using data from the 1971-1994 SEER Cancer Statistics Review. Results Of the 1852 persons, 1160 (63%) responded, or 75% (1160/1552) of those who received the survey. The total number of observed cancer cases in the PWS study population was 8 versus 4.80 expected in the general US population (P =.1610). Three cases of myeloid leukemia were observed versus 0.075 leukemias expected (P =.0001). Conclusions There appears to be an increased risk of myeloid leukemias, but not other cancers, among persons with PWS.
引用
收藏
页码:174 / 178
页数:5
相关论文
共 38 条
[1]   CLONAL HEMATOLOGIC DISORDERS IN DOWN-SYNDROME - A REVIEW [J].
AVETLOISEAU, H ;
MECHINAUD, F ;
HAROUSSEAU, JL .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1995, 17 (01) :19-24
[2]   GENETICS AND EPIDEMIOLOGY OF WILMS-TUMOR - THE FRENCH WILMS-TUMOR STUDY [J].
BONAITIPELLIE, C ;
CHOMPRET, A ;
TOURNADE, MF ;
HOCHEZ, J ;
MOUTOU, C ;
ZUCKER, JM ;
STESCHENKO, D ;
BRUNATMENTIGNY, M ;
ROCHE, H ;
TRON, P ;
FRAPPAZ, D ;
MUNZER, M ;
BACHELOT, C ;
DUSOL, F ;
SOMMELETOLIVE, D ;
LEMERLE, J .
MEDICAL AND PEDIATRIC ONCOLOGY, 1992, 20 (04) :284-291
[3]   PREVALENCE STUDY OF PRADER-WILLI SYNDROME IN NORTH-DAKOTA [J].
BURD, L ;
VESELY, B ;
MARTSOLF, J ;
KERBESHIAN, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 37 (01) :97-99
[4]   CLINICAL AND CYTOGENETIC SURVEY OF 39 INDIVIDUALS WITH PRADER-LABHART-WILLI SYNDROME [J].
BUTLER, MG ;
MEANEY, FJ ;
PALMER, CG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) :793-809
[5]   Prader-Willi syndrome [J].
Cassidy, SB .
JOURNAL OF MEDICAL GENETICS, 1997, 34 (11) :917-923
[6]   KLINEFELTER SYNDROME, TUMOR, AND SEXUAL PRECOCITY [J].
CHAUSSAIN, JL ;
LEMERLE, J ;
ROGER, M ;
JOB, JC .
JOURNAL OF PEDIATRICS, 1980, 97 (04) :607-609
[7]   SCREENING FOR WILMS-TUMOR IN HIGH-RISK INDIVIDUALS [J].
CLERICUZIO, CL ;
JOHNSON, C .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1995, 9 (06) :1253-+
[8]   DENYS-DRASH SYNDROME - RELATING A CLINICAL DISORDER TO GENETIC ALTERATIONS IN THE TUMOR-SUPPRESSOR GENE WT1 [J].
COPPES, MJ ;
HUFF, V ;
PELLETIER, J .
JOURNAL OF PEDIATRICS, 1993, 123 (05) :673-678
[9]   WILMS-TUMOR IN A PATIENT WITH PRADER-WILLI SYNDROME [J].
COPPES, MJ ;
SOHL, H ;
TESHIMA, IE ;
MUTIRANGURA, A ;
LEDBETTER, DH ;
WEKSBERG, R .
JOURNAL OF PEDIATRICS, 1993, 122 (05) :730-733
[10]  
COPPES MJ, 1994, NEW ENGL J MED, V331, P586