Familial association of pleuropulmonary blastoma with cystic nephroma and other renal tumors: A report from the international pleuropulmonary blastoma registry

被引:74
作者
Boman, Francoise
Hill, D. Ashley
Williams, Gretchen M.
Chauvenet, Allen
Fournet, Jean-Christophe
Soglio, Dorothee Bouron-Dal
Messinger, Yoav
Priest, John R.
机构
[1] Washington Univ, Med Ctr, Lauren V Ackerman Lab Surg Pathol, Barnes Jewish Hosp, St Louis, MO 63110 USA
[2] Washington Univ, Med Ctr, St Louis Childrens Hosp, St Louis, MO 63110 USA
[3] Univ Hosp Lille, Dept Pathol, Lille, France
[4] Childrens Hosp & Clin Minnesota, Dept Pediat Hematol Oncol, St Paul, MN USA
[5] Childrens Hosp & Clin Minnesota, Int Pleuropulm Blastoma Registry, St Paul, MN USA
[6] Wake Forest Univ, Dept Pediat, Med Ctr, Winston Salem, NC 27109 USA
[7] Hop St Justine, Dept Pathol, Montreal, PQ H3T 1C5, Canada
关键词
D O I
10.1016/j.jpeds.2006.08.068
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To characterize the association of pleuropulmonary blastoma (PPB) with cystic nephroma (CN) and other renal tumors. Study design Complete clinicopadhologic review of cases from the International PPB Registry and literature. Results We identified 18 patients with PPB associated with 20 renal tumors (15 CN), either in themselves or family members. All patients with PPB were < 5 years of age. All but one of the renal diagnoses were made before 4 years of age. Eleven children had both PPB and renal tumor, one of whom also had a sibling with CN. Six children with PPB alone had one or more family members with CN. The mother of one child with PPB had Wilms' tumor. Pulmonary disease was bilateral in four patients. Renal disease was bilateral in three patients. Two children with PPB and bilateral renal cystic tumors also had intussusceptions because of small bowel juvenile polyps. In six families, dysplasia/neoplasia affected organs other than lung and kidney. Conclusions CN or related tumors were found in 9.2% of 152 Registry-reviewed PPB cases. The occurrence of rare pulmonary and renal tumors together in patients and/or family members, the early age of onset, and the multiplicity of tumors is compatible with a constitutional genetic predisposition.
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页码:850 / 854
页数:5
相关论文
共 30 条
[1]  
ALLAN BT, 1987, CANCER, V59, P1005, DOI 10.1002/1097-0142(19870301)59:5<1005::AID-CNCR2820590526>3.0.CO
[2]  
2-5
[3]   Familial cystic nephroma in two siblings with pleuropulmonary blastoma [J].
Bal, N ;
Kayaselçuk, F ;
Polat, A ;
Bolat, F ;
Yilmaz, Z ;
Tuncer, I .
PATHOLOGY & ONCOLOGY RESEARCH, 2005, 11 (01) :53-56
[4]   PRECURSOR LESIONS OF WILMS-TUMOR - CLINICAL AND BIOLOGICAL IMPLICATIONS [J].
BECKWITH, JB .
MEDICAL AND PEDIATRIC ONCOLOGY, 1993, 21 (03) :158-168
[5]   A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5 [J].
BesnardGuerin, C ;
Newsham, I ;
Winqvist, R ;
Cavenee, WK .
HUMAN GENETICS, 1996, 97 (02) :163-170
[6]  
COTTINGHAM SL, 1995, UNPUB CYSTIC NEPHROM
[7]  
DEHNER LP, 1995, PERSPECT PEDIAT PATH, V18, P214
[8]  
DELAHUNT B, 1993, CANCER, V71, P1338, DOI 10.1002/1097-0142(19930215)71:4<1338::AID-CNCR2820710427>3.0.CO
[9]  
2-A
[10]  
Eble JN, 1998, SEMIN DIAGN PATHOL, V15, P2