Surgical Treatment of Patients with Rasmussen Encephalitis

被引:21
|
作者
Guan, Yuguang
Zhou, Jian
Luan, Guoming [1 ]
Liu, Xingzhou
机构
[1] Capital Med Univ, Beijing Sanbo Brain Hosp, Dept Neurosurg, Beijing 100093, Peoples R China
关键词
Rasmussen encephalitis; Hernispherectomy; Hemispherotomy; Epilepsy; FUNCTIONAL HEMISPHERECTOMY; IMMUNOMODULATORY THERAPY; INTRACTABLE EPILEPSY; SEIZURE; CHILDREN; LANGUAGE; SURGERY; ONSET; DIAGNOSIS; RECOVERY;
D O I
10.1159/000355901
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Rasmussen encephalitis (RE) is a rare progressive encephalitis that results in intractable seizures, cognitive decline and hemiparesis. Surgery seems to be the only effective way to control seizures in RE patients. Objective:To describe the clinical, electrophysiological, neuroradiological and histological findings of our patients with RE and to evaluate the outcome of their surgical treatment. Methods: A total of 20 patients were identified by the criteria of RE. Surgery was conducted in the left hemisphere in 6 patients and in the right hemisphere in 14. The surgical methods included anatomical hemispherectomy, functional hennispherectomy, hemispherotomy, lesion resection, multilobar resection, selective resection and bipolar electrocoagulation of functional cortexes. Results:The mean follow-up period was 5.45 years (range 3-8). After surgery, 16 patients (80%) were evaluated as being Engel class I. All of the patients had increases in cognitive abilities after surgery except 1 patient with bilateral RE. After surgery, most patients could walk independently, but the fine movement of the hands was lost. Postoperative hydrocephalus was observed in 1 patient after functional hemispherectomy, and there was no death in this series. Conclusion: Hemispherectomy and hemispherotonny were both confirmed as beneficial procedures in controlling seizures and improving quality of the life in RE cases. (c) 2014 S. Karger AG, Basel
引用
收藏
页码:86 / 93
页数:8
相关论文
共 50 条
  • [31] Bilateral Rasmussen encephalitis
    Guan, Yuguang
    Luan, Guoming
    Zhou, Jian
    Liu, Xingzhou
    EPILEPSY & BEHAVIOR, 2011, 20 (02) : 398 - 403
  • [32] Rasmussen's Encephalitis
    Luat, Aimee F.
    JOURNAL OF PEDIATRIC EPILEPSY, 2018, 7 (02) : 45 - 51
  • [33] Rasmussen's encephalitis
    Hart, Y
    EPILEPTIC DISORDERS, 2004, 6 (03) : 133 - 144
  • [34] CYTOMEGALOVIRUS AND RASMUSSEN ENCEPHALITIS
    POWER, C
    POLAND, SD
    BLUME, WT
    GIRVIN, JP
    RICE, GPA
    LANCET, 1990, 336 (8726): : 1282 - 1284
  • [35] Rasmussen Encephalitis: An Update
    Cay-Martinez, Karla C.
    Hickman, Richard A.
    McKhann, Guy M., II
    Provenzano, Frank A.
    Sands, Tristan T.
    SEMINARS IN NEUROLOGY, 2020, 40 (02) : 201 - 210
  • [36] CYTOMEGALOVIRUS AND RASMUSSEN ENCEPHALITIS
    FARRELL, MA
    CHENG, L
    CORNFORD, ME
    GRODY, WW
    VINTERS, HV
    LANCET, 1991, 337 (8756): : 1551 - 1552
  • [37] CYTOMEGALOVIRUS AND RASMUSSEN ENCEPHALITIS
    ROOTBERNSTEIN, RS
    LANCET, 1991, 337 (8735): : 239 - 240
  • [38] RASMUSSEN'S ENCEPHALITIS
    Bien, C.
    EPILEPSIA, 2010, 51 : 181 - 181
  • [39] Rasmussen's Encephalitis
    Timarova, G.
    Lisa, I.
    Mikula, P.
    Simko, M.
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2016, 79 (05) : 500 - 512
  • [40] Rasmussen encephalitis - A clinicopathologic and immunohistochemical study of seven patients
    Prayson, RA
    Frater, JL
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2002, 117 (05) : 776 - 782