Spontaneous resolution of Chiari malformation Type I in monozygotic twins

被引:16
|
作者
Miller, Jeffrey H. [2 ]
Limbrick, David D., Jr. [1 ]
Callen, Matthew [1 ]
Smyth, Matthew D. [1 ]
机构
[1] Washington Univ, Dept Neurosurg, St Louis, MO USA
[2] Washington Univ, Dept Neuroradiol, St Louis, MO USA
关键词
Chiari malformation; hindbrain hernia; monozygotic twins; spontaneous resolution;
D O I
10.3171/PED.2008.2.11.317
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The spontaneous resolution of isolated tonsillar ectopia in Chiari malformation Type I (CM-I) is a known and reported entity in 2 previous single study case reports. However, it has not been previously described in monozygotic twins. Two children, similar to 1 year of age with CM-I and presumed episodes of pallid syncope or breath-holding spells presented for neurosurgical evaluation. Although Chiari decompression was considered, the authors decided to proceed with conservative management with close follow-up due to the uncertain nature of these episodes. Approximately 4 years later, both children's symptoms had resolved. Repeated MR imaging examinations also showed spontaneous resolution of the malformation in both girls. These cases emphasize that when patients with CM-I present with atypical symptoms, spontaneous resolution or improvement is possible, which may influence the decision to pursue a trial of nonsurgical management. The possible pathophysiological mechanisms and genetic influences of CM-I are also briefly discussed. (DOI: 10.3171/PED.2008.2.11.317)
引用
收藏
页码:317 / 319
页数:3
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