Oncologic manifestations in children with neurofibromatosis type 1 in Turkey

被引:0
作者
Incecik, Faruk [1 ]
Altunbasak, Sakir [1 ]
Herguner, M. Ozlem [1 ]
Bayram, Ibrahim [2 ]
Kupeli, Serhan [3 ]
Demirbilek, Huseyin [4 ]
机构
[1] Cukurova Univ, Fac Med, Dept Pediat, Div Pediat Neurol, Adana, Turkey
[2] Cukurova Univ, Fac Med, Dept Pediat, Div Pediat Oncol, Adana, Turkey
[3] Diyarbakir State Childrens Hosp, Unit Pediat Oncol, Diyarbakir, Turkey
[4] Diyarbakir State Childrens Hosp, Dept Pediat, Diyarbakir, Turkey
关键词
Neurofibromatosis type 1; malignancy; children; OPTIC PATHWAY GLIOMAS; FOLLOW-UP; TUMORS; GENE; GLIOBLASTOMA; DOMAIN;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Children with neurofibromatosis type 1 (NF1) are predisposed to malignancies such as brain tumors, leukemia, and pheochromocytomas. The aim of this study was to evaluate malignancy in patients with NF1. We studied 120 patients with NF1 in this study. Demographic data from these patients were retrospectively reviewed. We found 20 malignancies in 19 patients in our study. Ten children with NF1 had optic glioma. Four children had solid central nervous system tumors (3 pilocytic astrocytomas, 1 glioblastoma multiforme). Three patients had myeloid malignancies (1 juvenile myelomonocytic leukemia, 1 acute myeloid leukemia, 1 acute lymphocytic leukemia). Hodgkin lymphoma, T-cell lymphoblastic lymphoma, and malignant triton tumor were found in one patient each. Patients with NF1 are predisposed to both benign and malignant tumors of neurogenic and non-neurogenic origin. Therefore, systematic medical follow-up in patients with NF1 is important.
引用
收藏
页码:266 / 270
页数:5
相关论文
共 24 条
  • [1] Growth rate characteristics of acoustic neuromas associated with neurofibromatosis type 2
    Abaza, MM
    Makariou, E
    Armstrong, M
    Lalwani, AK
    [J]. LARYNGOSCOPE, 1996, 106 (06) : 694 - 699
  • [2] NEUROFIBROMATOSIS AND CHILDHOOD LEUKEMIA
    BADER, JL
    MILLER, RW
    [J]. JOURNAL OF PEDIATRICS, 1978, 92 (06) : 925 - 929
  • [3] Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1
    Brems, Hilde
    Beert, Eline
    de Ravel, Thomy
    Legius, Eric
    [J]. LANCET ONCOLOGY, 2009, 10 (05) : 508 - 515
  • [4] BROOKS JSJ, 1985, CANCER-AM CANCER SOC, V55, P2543, DOI 10.1002/1097-0142(19850601)55:11<2543::AID-CNCR2820551105>3.0.CO
  • [5] 2-4
  • [6] A MAJOR SEGMENT OF THE NEUROFIBROMATOSIS TYPE-1 GENE - CDNA SEQUENCE, GENOMIC STRUCTURE, AND POINT MUTATIONS
    CAWTHON, RM
    WEISS, R
    XU, GF
    VISKOCHIL, D
    CULVER, M
    STEVENS, J
    ROBERTSON, M
    DUNN, D
    GESTELAND, R
    OCONNELL, P
    WHITE, R
    [J]. CELL, 1990, 62 (01) : 193 - 201
  • [7] Malignant Peripheral Nerve Sheath Tumors in Childhood: 13 Cases From a Single Center
    Demir, Haci Ahmet
    Varan, Ali
    Yalcin, Bilgehan
    Akyuz, Canan
    Kutluk, Tezer
    Buyukpamukcu, Munevver
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2012, 34 (03) : 204 - 207
  • [8] Fatal glioblastoma multiforme in a patient with neurofibromatosis type I:: the dilemma of systematic medical follow-up
    Distelmaier, Felix
    Fahsold, Raimund
    Reifenberger, Guido
    Messing-Juenger, Martina
    Schaper, Joerg
    Schneider, Dominik T.
    Goebel, Ulrich
    Mayatepek, Ertan
    Rosenbaum, Thorsten
    [J]. CHILDS NERVOUS SYSTEM, 2007, 23 (03) : 343 - 347
  • [9] Graf Norbert, 2010, Pediatr Blood Cancer, V54, P870, DOI 10.1002/pbc.22487
  • [10] GRIFA A, 1995, CLIN GENET, V47, P281