Diagnostic criteria for schwannomatosis

被引:250
作者
MacCollin, M
Chiocca, EA
Evans, DG
Friedman, JM
Horvitz, R
Jaramillo, D
Lev, M
Mautner, VF
Niimura, M
Plotkin, SR
Sang, CN
Stemmer-Rachamimov, A
Roach, ES
机构
[1] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[4] Ohio State Univ, Ctr Med, Dept Neurosurg, Columbus, OH 43210 USA
[5] St Marys Hosp, Dept Genet, Manchester M13 0JH, Lancs, England
[6] Univ British Columbia, Dept Med Genet, Vancouver, BC V5Z 1M9, Canada
[7] Natl Neurofibromatosis Fdn, New York, NY USA
[8] Univ Hamburg Hosp, Dept Neurol, D-2000 Hamburg, Germany
[9] Rinshoiyaku Inc, Tokyo, Japan
[10] Brigham & Womens Hosp, Dept Anesthesia, Boston, MA 02115 USA
[11] Wake Forest Univ, Div Child Neurol, Winston Salem, NC 27109 USA
关键词
D O I
10.1212/01.WNL.0000163982.78900.AD
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The neurofibromatoses are a diverse group of genetic conditions that share a predisposition to the development of tumors of the nerve sheath. Schwannomatosis is a recently recognized third major form of neurofibromatosis (NF) that causes multiple schwannomas without vestibular tumors diagnostic of NF2. Patients with schwannomatosis represent 2.4 to 5 % of all patients requiring schwannoma resection and approximately one third of patients with schwannomatosis have anatomically localized disease with tumors limited to a single limb or segment of spine. Epidemiologic studies suggest that schwannomatosis is as common as NF2, but that familial occurrence is inexplicably rare. Patients with schwannomatosis overwhelmingly present with pain, and pain remains the primary clinical problem and indication for surgery. Diagnostic criteria for schwannomatosis are needed for both clinicians and researchers, but final diagnostic certainly will await the identification of the schwannomatosis locus itself.
引用
收藏
页码:1838 / 1845
页数:8
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