Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation

被引:22
|
作者
Chantrain, Christophe F.
Jijon, Priscilla
De Raedt, Thomas
Vermylen, Christiane
Poirel, Helene A.
Legius, Eric
Brichard, Benedicte
机构
[1] Catholic Univ Louvain, St Luc Univ Hosp, Dept Pediat Hematol Oncol, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
[3] Catholic Univ Louvain, St Luc Univ Hosp, Ctr Med Genet, Hematol Sect, B-1200 Brussels, Belgium
关键词
acute myelomonocytic leukemia; leukemogenesis; neuroblastoma; Noonan syndrome; PTPN11; 7q deletion;
D O I
10.1002/pbc.20527
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A 4-year-old girl with Noonan syndrome (NS) and constitutive PTPN11 mutation presented with stage 4 neuroblastoma and was treated by intensive chemotherapy. During the treatment, cytogenetic analysis revealed the development of a hyperdiploid clone with duplication of the germline PTPN11 mutation in a morphologically normal bone marrow. A few months later, the patient developed acute myelomonoblastic leukemia with an additional clonal deletion of 7q. Although, we cannot conclude whether there is an association between NS and neuroblastoma, this case suggests that duplication of germline PTPN11 mutations, potentially induced by chemotherapy, contributes to leukemogenesis in patients with NS.
引用
收藏
页码:101 / 104
页数:4
相关论文
共 50 条
  • [21] Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation
    Jongmans, Marjolijn C. J.
    van der Burgt, Ineke
    Hoogerbrugge, Peter M.
    Noordam, Kees
    Yntema, Helger G.
    Nillesen, Willy M.
    Kuiper, Roland P.
    Ligtenberg, Marjolijn J. L.
    van Kessel, Ad Geurts
    van Krieken, J. Han J. M.
    Kiemeney, Lambertus A. L. M.
    Hoogerbrugge, Nicoline
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (08) : 870 - 874
  • [22] PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning
    Els Schollen
    Gert Matthijs
    Marc Gewillig
    Jean-Pierre Fryns
    Eric Legius
    European Journal of Human Genetics, 2003, 11 : 85 - 88
  • [23] Phenotype variability in Noonan syndrome patients with and without PTPN11 mutation
    Ferreira, Lize V.
    Souza, Silvia A. L.
    Montenegro, Luciana R.
    Arnhold, Ivo J. P.
    Pasqualini, Titania
    Heinrich, Juan Jorge
    Keselman, Ana Claudia
    Mendonca, Berenice B.
    Jorge, Alexander A. L.
    ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA, 2007, 51 (03) : 450 - 456
  • [24] Mild variable Noonan syndrome in a family with a novel PTPN11 mutation
    Zenker, Martin
    Voss, Egbert
    Reis, Andre
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2007, 50 (01) : 43 - 47
  • [25] PTPN11 mutation in a young man with Noonan syndrome and Retinitis Pigmentosa
    Schollen, E
    Matthijs, G
    Fryns, JF
    GENETIC COUNSELING, 2003, 14 (02): : 259 - 259
  • [26] A mother and son with Noonan syndrome resulting from a PTPN11 mutation
    Derbent, Murat
    TURKISH JOURNAL OF PEDIATRICS, 2011, 53 (01) : 117 - 117
  • [27] Prognostic Impact of PTPN11 mutations in Acute Myeloid Leukemia
    Ho, Thuy
    Kicklighter, Luke
    Avetian, George
    Murray, Graeme F.
    Bouligny, Ian M.
    Lee, Hyun
    Dziarnowski, Natasha
    Maher, Keri
    BLOOD, 2024, 144 : 6120 - 6121
  • [28] A PTPN11 mutation in a woman with Noonan syndrome and protein-losing enteropathy
    Wang, Na
    Shi, Wen
    Jiao, Yang
    BMC GASTROENTEROLOGY, 2020, 20 (01)
  • [29] Noonan syndrome: Prenatal diagnosis in a woman carrying a PTPN11 gene mutation
    Celia Gonzalez-Huerta, Norma
    Manuel Valdes-Miranda, Juan
    Perez-Cabrera, Adrian
    Pacheco-Cuellar, Guillermo
    Maria Gonzalez-Huerta, Luz
    Alberto Cuevas-Covarrubias, Sergio
    JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2010, 23 (07): : 688 - 691
  • [30] Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation
    Bertola, DR
    Pereira, AC
    de Oliveira, PSL
    Kim, CA
    Krieger, JE
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 130A (04) : 378 - 383