Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation

被引：12
|
作者：
Yetgin, S. [1 ]
Olcay, L. [2 ]
Koc, A. [3 ]
Germeshausen, M. [4 ]
机构：
[1] Hacettepe Univ, Dept Pediat Hematol, Med Ctr, Ankara, Turkey
[2] Oncol State Hosp, Ankara, Turkey
[3] Harran Univ, Dept Pediat Hematol, Urfa, Sanliurfa, Turkey
[4] Hannover Med Sch, Dept Pediat Hematol & Oncol, D-3000 Hannover, Germany
来源：
LEUKEMIA | 2008年 / 22卷 / 09期
关键词：
D O I：
10.1038/leu.2008.64
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
[No abstract available]
引用
收藏
页码：1797 / 1797
页数：1
相关论文
共 50 条
  • [1] Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation
    S Yetgin
    L Olcay
    A Koç
    M Germeshausen
    Leukemia, 2008, 22 : 1797 - 1797
  • [2] HAX1 mutation in an infant with severe congenital neutropenia
    Eghbali, Aziz
    Eshghi, Peyman
    Malek, Fatemeh
    Abdollahpour, Hengameh
    Rezaei, Nima
    TURKISH JOURNAL OF PEDIATRICS, 2010, 52 (01) : 81 - 84
  • [3] A novel compound heterozygous HAX1 mutation in a Chinese patient with severe congenital neutropenia and chronic myelomonocytic leukemia transformation but without neurodevelopmental abnormalities
    Xue, Sheng-Li
    Li, Jin-Li
    Zou, Jing-Ying
    Su, Jian
    Chen, Su-Ning
    Wu, De-Pei
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2012, 97 (02): : 318 - 320
  • [4] A point mutation in the genomic G-CSF receptor gene in a patient with severe congenital neutropenia
    Yokoyama, T
    Okamura, S
    Kanaji, T
    Asano, Y
    Nakashima, H
    Mizuno, Y
    Okamura, J
    Niho, Y
    EXPERIMENTAL HEMATOLOGY, 1996, 24 (09) : 271 - 271
  • [5] SEVERE CONGENITAL NEUTROPENIA IN TWO SIBLINGS RELATED TO HAX1 MUTATION WITHOUT NEURODEVELOPMENTAL DISORDERS
    Patiroglu, T.
    Gungor, H. Eke
    Triot, A.
    Unal, E.
    GENETIC COUNSELING, 2013, 24 (03): : 253 - 258
  • [6] Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
    Tham Thi Tran
    Quang Van Vu
    Wada, Taizo
    Yachie, Akihiro
    Huong Le Thi Minh
    Sang Ngoc Nguyen
    CASE REPORTS IN PEDIATRICS, 2018, 2018
  • [7] Acquired substitution mutation in G-CSF receptor underlying evolution of severe congenital neutropenia to acute myelogenous leukemia.
    Aprikyan, AAG
    Rodger, ER
    Jeha, S
    Boxer, LA
    Dale, DC
    BLOOD, 2000, 96 (11) : 185B - 185B
  • [8] A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia
    Goktas, Serdar
    Azizoglu, Zehra B.
    Petersheim, Daniel
    Erdogan, Merve
    Eke Gungor, Hatice
    Bisgin, Atil
    Tug Bozdogan, Sevcan
    Eken, Ahmet
    Unal, Ekrem
    Klein, Christoph
    Patiroglu, Turkan
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2022, 44 (01) : E62 - E67
  • [9] Acquired G-CSF receptor mutation in myeloid progenitor cells in a patient with acute myeloid leukemia secondary to congenital neutropenia.
    Sauer, S
    Ballmaier, M
    Welte, K
    Germeshausen, M
    BLOOD, 2003, 102 (11) : 276A - 276A
  • [10] A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations
    Muhammad Faiyaz-Ul-Haque
    Abdullah Al-Jefri
    Fouad Al-Dayel
    Jalaluddin A. K. M. Bhuiyan
    Hala A. Abalkhail
    Randa Al-Nounou
    Ahmed Al-Abdullatif
    Monogaran S. Pulicat
    Ameera Gaafar
    Ayodele A. Alaiya
    Iskra Peltekova
    Syed H. E. Zaidi
    European Journal of Pediatrics, 2010, 169 : 661 - 666
12345