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丙酸和甲基丙二酸代谢紊乱时的脑部CT和磁共振成像

CT and MR of the brain in disorders of the propionate and methylmalonate metabolism.

作者信息

Brismar J, Ozand P T

机构信息

Department of Diagnostic Radiology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

出版信息

AJNR Am J Neuroradiol. 1994 Sep;15(8):1459-73.

Abstract

PURPOSE

To present the CT and MR findings in children with propionic and methylmalonic acidemia.

METHODS

Twenty-three new patients with methylmalonic and 20 with propionic acidemia were examined with CT and/or MR of the brain. In total 52 CT and 55 MR studies were done. Twenty-six previously published cases were also reviewed.

RESULTS

The findings were similar in the two syndromes. During the first month of life the examinations were either normal or showed white matter attenuation. Later during the first year moderate or even severe widening of sulci and fissures was seen, especially in infants with propionic acidemia. During therapy, these changes often resolved, especially in the patients with methylmalonic acidemia. Mild to moderate delay in myelination was also a common finding in both disorders. Basal ganglia changes, predominately in the globus pallidus, were seen in five patients with methylmalonic acidemia and in two children with propionic acidemia; in two patients these changes were transient.

CONCLUSION

Children who have methylmalonic or propionic acidemia, in addition to widening of cerebrospinal fluid spaces and some delay in myelination, also often show symmetric involvement of the basal ganglia.

摘要

目的

阐述丙酸血症和甲基丙二酸血症患儿的CT及MR表现。

方法

对23例甲基丙二酸血症新发病例和20例丙酸血症新发病例进行脑部CT和/或MR检查。共进行了52次CT检查和55次MR检查。还回顾了26例先前发表的病例。

结果

两种综合征的表现相似。在出生后的第一个月内,检查结果要么正常,要么显示白质密度减低。在出生后的第一年后期,可见脑沟和脑裂中度甚至重度增宽,尤其是丙酸血症患儿。在治疗过程中,这些改变常常消退,尤其是甲基丙二酸血症患儿。轻度至中度髓鞘形成延迟在两种疾病中也是常见表现。5例甲基丙二酸血症患儿和2例丙酸血症患儿可见基底节改变,主要累及苍白球;其中2例患儿的这些改变是短暂的。

结论

患有甲基丙二酸血症或丙酸血症的患儿,除了脑脊液间隙增宽和髓鞘形成有一定延迟外,还常表现为基底节对称性受累。

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