Predictors of vestibular schwannoma growth in patients with neurofibromatosis Type 2

被引:78
作者
Baser, ME
Makariou, EV
Parry, DM
机构
[1] Georgetown Univ, Med Ctr, Dept Radiol, Washington, DC 20007 USA
[2] Natl Canc Inst, Genet Epidemiol Branch, Bethesda, MD USA
关键词
natural history; neurogenetics; neurofibromatosis Type 2; vestibular schwannoma;
D O I
10.3171/jns.2002.96.2.0217
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. The results of two longitudinal studies of growth rates of vestibular schwannomas (VSs) in patients with neurofibromatosis Type 2 (NF2) differ as to whether VS growth rates decrease or increase with increasing patient age. The authors undertook this study to assess the relationship between VS growth rates and patient age and type of constitutional NF2 mutation they also examined variability in VS growth rates among multiple patients in families with NF2. Methods. Gadolinium-enhanced magnetic resonance images obtained in 18 patients with inherited NF2 from 11 unrelated families were retrospectively analyzed. The patients had been observed for a median of 4 years. Volumes of the VSs were measured using a two-component box model (intrameatal and extrameatal parts measured separately). Single-strand conformation polymorphism analysis and Southern blot analysis were used to identify constitutional NF2 mutations. Growth rates of the VSs were highly variable, but tended to decrease with increasing patient age both at onset of signs or symptoms of NF2 (r(2) = 0.35, p = 0.026) and at diagnosis (r(2) = 0.33, p = 0.012). The VS growth rates did not vary significantly with the type of constitutional NF2 mutation or the number of non-VS cerebral or spinal tumors. The VS growth rates were highly variable within families and did not correspond to clinical indices of NF2 disease severity, such as patient age at symptom onset and the number of non-VS cerebral and spinal tumors. Conclusions. The growth rates of VSs in patients with NF2 are highly variable, but tend to decrease with increasing patient age. Clinical treatment of multiple patients in families with NF2 cannot be based on the expectations of similar VS growth rates, even when other clinical aspects of disease severity are similar.
引用
收藏
页码:217 / 222
页数:6
相关论文
共 26 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] PROLIFERATIVE POTENTIAL OF SPORADIC AND NEUROFIBROMATOSIS 2-ASSOCIATED SCHWANNOMAS AS STUDIED BY MIB-1 (KI-67) AND PCNA LABELING
    ANTINHEIMO, J
    HAAPASALO, H
    SEPPALA, M
    SAINIO, M
    CARPEN, O
    JAASKELAINEN, J
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (06) : 776 - 782
  • [3] Baser ME, 1996, AM J MED GENET, V64, P563, DOI 10.1002/(SICI)1096-8628(19960906)64:4<563::AID-AJMG7>3.0.CO
  • [4] 2-Q
  • [5] CONSERVATIVE TREATMENT OF PATIENTS WITH ACOUSTIC TUMORS
    BEDERSON, JB
    VONAMMON, K
    WICHMANN, WW
    YASARGIL, MG
    [J]. NEUROSURGERY, 1991, 28 (05) : 646 - 651
  • [6] ACOUSTIC NEUROMA (VESTIBULAR SCHWANNOMA) - GROWTH AND SURGICAL AND NONSURGICAL CONSEQUENCES OF THE WAIT-AND-SEE POLICY
    CHARABI, S
    THOMSEN, J
    MANTONI, M
    CHARABI, B
    JORGENSEN, B
    BORGESEN, SE
    GYLDENSTED, C
    TOS, M
    [J]. OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1995, 113 (01) : 5 - 14
  • [7] Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations
    Evans, DGR
    Trueman, L
    Wallace, A
    Collins, S
    Strachan, T
    [J]. JOURNAL OF MEDICAL GENETICS, 1998, 35 (06) : 450 - 455
  • [8] EVANS DGR, 1992, Q J MED, V84, P603
  • [9] The size of acoustic neuromas: CT and MRI
    Fiirgaard, B
    Pedersen, CB
    Lundorf, E
    [J]. NEURORADIOLOGY, 1997, 39 (08) : 599 - 601
  • [10] Kluwe L, 1998, AM J MED GENET, V77, P228, DOI 10.1002/(SICI)1096-8628(19980518)77:3<228::AID-AJMG8>3.0.CO