An autopsy case of caudate nucleus lobulation accompanied with diaphragmatic eventration

被引:1
作者
Hamano, K
Kumada, S
Hayashi, M
Kurano, N
Uchiyama, A
Kurata, K
机构
[1] Metropolitan Fuchu Med Ctr Severe Motor & Intelle, Dept Pediat, Fuchu, Tokyo 1830042, Japan
[2] Tokyo Metropolitan Neurol Hosp, Tokyo, Japan
[3] Tokyo Metropolitan Inst Neurosci, Dept Clin Neuropathol, Tokyo, Japan
关键词
diaphragmatic eventration; caudate nucleus anomaly; pyramidal tract hypoplasia; skeletal anomaly; meningioma;
D O I
10.1016/j.braindev.2005.11.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We describe an autopsy female case of multiple anomalies with lobulation of caudate nucleus tail, diaphragmatic eventration, skeletal anomalies, pyramidal tract anomaly, and meningothelial meningioma. Her psychomotor development was delayed, and she developed bilateral eventration of the diaphragms on X-ray film in her third decades. Right hemi-colonectomy was performed for volvulus at the age of 44 years, and meningioma was incidentally identified. She died at the age of 47 years. Autopsy demonstrated the partial deficiency of the muscular tissue in the circular thinned membranous area predominantly on left side including the central tendon of the diaphragm. The tails of the bilateral caudate nucleus demonstrated excessive lobulations, and the brainstern pyramidal tract showed hypoplasia. Immunoreactivity for tyrosine hydroxylase was deficient in the lobulated tail of caudate. We believe that this case is characterized by a rare combination of eventration, skeletal and nervous anomalies. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:401 / 404
页数:4
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