A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes

被引:46
作者
Scollon, Sarah [1 ]
Anglin, Amanda Knoth [2 ]
Thomas, Martha [3 ]
Turner, Joyce T. [4 ]
Schneider, Kami Wolfe [5 ]
机构
[1] Texas Childrens Hosp, Dept Pediat, Baylor Coll Med, Texas Childrens Canc Ctr, 1102 Bates St,FC 1200, Houston, TX 77030 USA
[2] Myriad Genet Labs, Dayton, OH USA
[3] Univ Virginia, Charlottesville, VA USA
[4] Childrens Natl Med Ctr, Dept Genet & Metab, Washington, DC 20010 USA
[5] Univ Colorado, Childrens Hosp Colorado, Dept Pediat, Ctr Canc & Blood Disorders, Aurora, CO USA
关键词
Pediatric cancer predisposition; Genetics; Genetic testing; Tumors; Cancer;
D O I
10.1007/s10897-017-0077-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
An understanding of the role of inherited cancer predisposition syndromes in pediatric tumor diagnoses continues to develop as more information is learned through the application of genomic technology. Identifying patients and their relatives at an increased risk for developing cancer is an important step in the care of this patient population. The purpose of this review is to highlight various tumor types that arise in the pediatric population and the cancer predisposition syndromes associated with those tumors. The review serves as a guide for recognizing genes and conditions to consider when a pediatric cancer referral presents to the genetics clinic.
引用
收藏
页码:387 / 434
页数:48
相关论文
共 508 条
  • [1] Loss of SUFU Function in Familial Multiple Meningioma
    Aavikko, Mervi
    Li, Song-Ping
    Saarinen, Silva
    Alhopuro, Pia
    Kaasinen, Eevi
    Morgunova, Ekaterina
    Li, Yilong
    Vesanen, Kari
    Smith, Miriam J.
    Evans, D. Gareth R.
    Poyhonen, Minna
    Kiuru, Anne
    Auvinen, Anssi
    Aaltonen, Lauri A.
    Taipale, Jussi
    Vahteristo, Pia
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 91 (03) : 520 - 526
  • [2] Frequent β-catenin mutations in juvenile nasopharyngeal angiofibromas
    Abraham, SC
    Montgomery, EA
    Giardiello, FM
    Wu, TT
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (03) : 1073 - 1078
  • [3] Update on retinoblastoma
    Abramson, DH
    Schefler, AC
    [J]. RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2004, 24 (06): : 828 - 848
  • [4] Multiple familial and pigmented basal cell carcinomas in early childhood - Bazex-Dupre-Christol syndrome
    Abuzahra, F.
    Parren, L. J. M. T.
    Frank, J.
    [J]. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2012, 26 (01) : 117 - 121
  • [5] Alexander G A, 1981, J Natl Med Assoc, V73, P1047
  • [6] Familial thyroid cancer
    Alsanea, O
    Clark, OH
    [J]. CURRENT OPINION IN ONCOLOGY, 2001, 13 (01) : 44 - 51
  • [7] Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2
    Alter, Blanche P.
    Rosenberg, Philip S.
    Brody, Lawrence C.
    [J]. JOURNAL OF MEDICAL GENETICS, 2007, 44 (01) : 1 - 9
  • [8] Fanconi anemia and the development of leukemia
    Alter, Blanche P.
    Clinician, Senior
    [J]. BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2014, 27 (3-4) : 214 - 221
  • [9] Squamous cell carcinomas in patients with Fanconi anemia and dyskeratosis congenita: A search for human papillomavirus
    Alter, Blanche P.
    Giri, Neelam
    Savage, Sharon A.
    Quint, Wim G. V.
    de Koning, Maurits N. C.
    Schiffman, Mark
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2013, 133 (06) : 1513 - 1515
  • [10] Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study
    Alter, Blanche P.
    Giri, Neelam
    Savage, Sharon A.
    Peters, June A.
    Loud, Jennifer T.
    Leathwood, Lisa
    Carr, Ann G.
    Greene, Mark H.
    Rosenberg, Philip S.
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2010, 150 (02) : 179 - 188