Syrinx resolution after posterior fossa decompression in patients with scoliosis secondary to Chiari malformation type I

被引:42
|
作者
Wu, Tao [1 ]
Zhu, Zezhang [1 ]
Jiang, Jian [2 ]
Zheng, Xin [1 ]
Sun, Xu [1 ]
Qian, Bangping [1 ]
Zhu, Feng [1 ]
Qiu, Yong [1 ]
机构
[1] Nanjing Univ, Dept Spine Surg, Affiliated Drum Tower Hosp, Sch Med, Nanjing 210008, Jiangsu, Peoples R China
[2] Nanjing Univ, Dept Neurosurg, Affiliated Drum Tower Hosp, Sch Med, Nanjing 210008, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Resolution; Syrinx; Chiari malformation type I; Syringomyelia; Scoliosis; Posterior fossa decompression; FORAMEN MAGNUM DECOMPRESSION; SURGICAL-TREATMENT; SUBOCCIPITAL DECOMPRESSION; PEDIATRIC-PATIENTS; SYRINGOMYELIA; EXPERIENCE; DURAPLASTY;
D O I
10.1007/s00586-011-2064-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Description of syrinx resolution after posterior fossa decompression (PFD) in patients with scoliosis secondary to Chiari malformation type I (CMI) and syringomyelia (SM) has been rarely reported in the literature. This study was performed to investigate the outcome of PFD in patients with scoliosis secondary to CMI and to identify potential predictive factors for better outcome after PFD. Patients with scoliosis secondary to CMI and SM, who had undergone PFD during the period 2000 through 2009, were recruited. Inclusion criteria were (1) age a parts per thousand currency sign 18 years, (2) diagnosis of SM associated with CMI, (3) scoliosis as the first complaint, (4) having undergone preoperative and follow-up magnetic resonance imaging (MRI). Patients with acquired CMI anomalies or who had received syringosubarachnoid shunting were excluded. The maximal S/C ratio and syrinx length were measured to evaluate syrinx resolution after PFD. A 20% decrease in S/C ratio or length at the latest follow-up was defined as a significant radiographic improvement and complete resolution was used to describe the syrinx disappearing after PFD. 44 patients were recruited. Follow-up MRI was conducted for all 44 patients at 6 +/- A 3 months postoperatively, for 37 patients at 2 years +/- A 3 months, for 26 patients at 4 years +/- A 3 months, and for 15 patients at 6 years +/- A 3 months. 97.7% (43 of 44) of patients showed significant radiographic improvement by MRI. The distance of tonsillar descent (mm) was correlated significantly with the surgical outcome (r = 0.116, P = 0.013). Significant improvement was observed within 6 months postoperatively, with continued slow improvement after that. Syringes showed significant improvement after PFD in most patients with scoliosis secondary to CMI. Resolution generally occurred within 6 months follow-up and continued at a slow rate for several years. In addition, the severity of tonsillar descent is a potential predictor for better improvement after standard PFD.
引用
收藏
页码:1143 / 1150
页数:8
相关论文
共 50 条
  • [31] Posterior fossa decompression and reconstruction in adolescents and adults with the Chiari I malformation
    Oro, John J.
    Mueller, Diane M.
    NEUROLOGICAL RESEARCH, 2011, 33 (03) : 261 - 271
  • [32] Comparison of surgical outcomes in patients with Chiari Type I malformation receiving posterior fossa decompression with and without duraplasty
    Butensky, Samuel
    Rodgers, Shaun
    Baron, Shanna
    Schneider, Steven
    Mittler, Mark
    CHILDS NERVOUS SYSTEM, 2020, 36 (07) : 1399 - 1405
  • [33] Comparison of surgical outcomes in patients with Chiari Type I malformation receiving posterior fossa decompression with and without duraplasty
    Samuel Butensky
    Shaun Rodgers
    Shanna Baron
    Steven Schneider
    Mark Mittler
    Child's Nervous System, 2020, 36 : 1399 - 1405
  • [34] Surgical outcomes after posterior fossa decompression with and without duraplasty in Chiari malformation-I
    Chotai, Silky
    Medhkour, Azedine
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2014, 125 : 182 - 188
  • [35] Response of Syrinx Associated with Chiari I Malformation to Posterior Fossa Decompression with or without Duraplasty and Correlation with Functional Outcome: A Prospective Study of 22 Patients
    Kumar, Anil
    Pruthi, Nupur
    Devi, B. Indira
    Gupta, Arun Kumar
    JOURNAL OF NEUROSCIENCES IN RURAL PRACTICE, 2018, 9 (04) : 587 - 592
  • [36] POSTERIOR-FOSSA VOLUME AND RESPONSE TO SUBOCCIPITAL DECOMPRESSION IN PATIENTS WITH CHIARI-I MALFORMATION
    BADIE, B
    MENDOZA, D
    BATZDORF, U
    NEUROSURGERY, 1995, 37 (02) : 214 - 218
  • [37] Spontaneous resolution of a Chiari malformation Type I and syrinx after supratentorial craniotomy for excision of a cavernous malformation
    Miele, William R.
    Schirmer, Clemens M.
    Yao, Kevin C.
    Heilman, Carl B.
    JOURNAL OF NEUROSURGERY, 2012, 116 (05) : 1054 - 1059
  • [38] Resolution of syringomyelia in ten cases of "up-and-down Chiari malformation" after posterior fossa decompression
    Goncalves da Silva, Jose Alberto
    Santiago Melo, Luiz Ricardo
    de Araujo, Antonio Fernandes
    dos Santos, Adailton Arcanjo, Jr.
    ARQUIVOS DE NEURO-PSIQUIATRIA, 2010, 68 (05) : 694 - 699
  • [39] Posterior fossa volume in children with Chiari malformation Type I
    Sgouros, Spyros
    Kountouri, Melpomeni
    Natarajan, Kal
    JOURNAL OF NEUROSURGERY, 2006, 105 (02) : 101 - 106
  • [40] Scoliosis in patients with Chiari malformation type I
    Noureldine, Mohammad Hassan A.
    Shimony, Nir
    Jallo, George I.
    Groves, Mari L.
    CHILDS NERVOUS SYSTEM, 2019, 35 (10) : 1853 - 1862