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
  • [41] Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive)
    Uçar, C
    Çalybkan, Ü
    Martini, S
    Heinritz, W
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2006, 28 (03) : 123 - 125
  • [42] Transient juvenile myelomonocytic leukemia in the setting of PTPN11 mutation and Noonan syndrome with secondary development of monosomy 7
    O'Halloran, Katrina
    Ritchey, A. Kim
    Djokic, Miroslav
    Friehling, Erika
    PEDIATRIC BLOOD & CANCER, 2017, 64 (07)
  • [43] Expanding the Clinical Spectrum of Ocular Anomalies in Noonan Syndrome: Axenfeld-Anomaly in a Child with PTPN11 Mutation
    Guerin, Andrea
    So, Joyce
    Mireskandari, Kamiar
    Jougeh-Doust, Soghra
    Chisholm, Caitlin
    Klatt, Regan
    Richer, Julie
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (02) : 403 - 406
  • [44] Azacitidine and Sorafenib Therapy in a Pediatric Patient With Refractory Acute Myeloid Leukemia With Monosomy 7 and Somatic PTPN11 Mutation
    Dahl, Nathan A.
    Michaels, Samantha T.
    McMasters, Richard L.
    Chandra, Sharat
    O'Brien, Maureen M.
    PEDIATRIC BLOOD & CANCER, 2016, 63 (03) : 551 - 553
  • [45] Probable Noonan syndrome in a boy without PTPN11 mutation, manifesting unusual complications
    Sumi, Muneichiro
    Ohno, Yasuharu
    Sasaki, Rie
    Kondoh, Tatsuro
    Tagawa, Masato
    Masuzaki, Hideaki
    Moriuchi, Hiroyuki
    PEDIATRICS INTERNATIONAL, 2009, 51 (01) : 138 - 140
  • [46] Mutational Patterns and Clonal Architecture of Therapy-Related Acute Myeloid Leukemia
    Awada, Hassan
    Kuzmanovic, Teodora
    Kishtagari, Ashwin
    Durrani, Jibran
    Durmaz, Arda
    Hong, Sanghee
    Kerr, Cassandra M.
    Adema, Vera
    Guan, Yihong
    Sandhu, Sonia
    Nazha, Aziz
    Meggendorfer, Manja
    Haferlach, Torsten
    Carraway, Hetty E.
    Sekeres, Mikkael A.
    Visconte, Valeria
    Maciejewski, Jaroslaw P.
    BLOOD, 2019, 134
  • [47] Severe aortic valvar stenosis in familial Noonan syndrome with mutation of the PTPN11 gene
    Abadir, Sylvia
    Edouard, Thomas
    Julia, Sophie
    CARDIOLOGY IN THE YOUNG, 2007, 17 (01) : 95 - 97
  • [48] Cochlear implantation and clinical features in patients with Noonan syndrome and Noonan syndrome with multiple lentigines caused by a mutation in PTPN11
    van Nierop, Josephine W. I.
    van Trier, Dorothee C.
    van der Burgt, Ineke
    Draaisma, Jos M. T.
    Mylanus, Emmanuel A. M.
    Snik, Ad F.
    Admiraal, Ronald J. C.
    Kunst, Henricus P. M.
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2017, 97 : 228 - 234
  • [49] PTPN11 mutations and Outcomes in Adult Patients with Acute Myeloid Leukemia
    Metzeler, Klaus H.
    Rothenberg-Thurley, Maja
    Gorlich, Dennis
    Sauerland, Maria Cristina
    Dufour, Annika Maria
    Schneider, Stephanie
    Subklewe, Marion
    Braess, Jan
    Wormann, Bernhard J.
    Berdel, Wolfgang E.
    Krug, Utz
    Hiddemann, Wolfgang
    Spiekermann, Karsten
    Herold, Tobias
    BLOOD, 2020, 136
  • [50] ANOPTHALMIA AND DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOURS IN A FAMILY WITH NOONAN SYNDROME AND A NOVEL PTPN11 MUTATION
    Mir, R.
    Chong, K.
    Benett, C.
    Aldin, A.
    Balen, F.
    Kraus, A.
    Taylor, R.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (11): : E35 - E35