LEOPARD Syndrome and Chiari Type I Malformation A Case Report and Review of the Literature

被引:13
作者
Beier, Alexandra D. [1 ]
Barrett, Ryan J. [1 ]
Burke, Kelly [2 ]
Kole, Bruce [2 ]
Soo, Teck M. [1 ]
机构
[1] Providence Hosp & Med Ctr, Dept Neurosurg, Southfield, MI 48075 USA
[2] Providence Hosp & Med Ctr, Dept Neurol, Southfield, MI 48075 USA
关键词
LEOPARD syndrome; Noonan syndrome; Chiari type I malformation (CM-1); dysphagia; syringomyelia; percutaneous endoscopic gastrostomy (PEG) tube; MULTIPLE LENTIGINES SYNDROME; NOONAN-SYNDROME; DYSPHAGIA; PTPN11; PATHOGENESIS; MUTATIONS; FOSSA;
D O I
10.1097/NRL.0b013e31817833c4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The authors present a 31-year-old man with a Chiari type I malformation (CM-1) occurring in conjunction with LEOPARD syndrome. He presented with severe dysphagia requiring placement of a percutaneous endoscopic gastrostomy (PEG) tube. Evaluation included magnetic resonance imaging (MRI) of the brain and cervical spine that revealed CM-1 with an extensive cervical syrinx. The patient underwent a suboccipital craniectomy with C1 laminectomy and duraplasty. His symptoms quickly resolved and his PEG tube was removed. Discussion: The occurrence of a CM-1 with LEOPARD syndrome has only been reported once, whereas CM-1 and Noonan syndrome have been linked in several cases. The similarity between LEOPARD and Noonan syndromes has been reported and many propose they represent 2 entities along a spectrum. Conclusion: In light of this spectrum, we propose that CM-1 should be considered in all patients presenting with LEOPARD-Noonan syndrome.
引用
收藏
页码:37 / 39
页数:3
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