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黏多糖贮积症患者脑部的磁共振成像

MR imaging of the brain in patients with mucopolysaccharidosis.

作者信息

Murata R, Nakajima S, Tanaka A, Miyagi N, Matsuoka O, Kogame S, Inoue Y

机构信息

Department of Pediatrics, Osaka City University Medical School, Japan.

出版信息

AJNR Am J Neuroradiol. 1989 Nov-Dec;10(6):1165-70.

Abstract

MR imaging of the brain was performed in eight patients with mucopolysaccharidosis (MPS). Two had MPS I S, one had MPS IIA, two had MPS IIB, two had MPS IIIB, and one had MPS VI. In the patients with MPS IIA and MPS VI, T1 and T2 were prolonged in various areas of the cerebral white matter. These findings seemed to correspond with the development of pathologic changes in MPS, such as perivascular pits in the white matter observed on slices of the fixed brain. In the patients with MPS IIA and MPS IIIB, the white matter did not show the proper signal intensity, which suggested that myelination was insufficient and that infiltration or deposition of glycosaminoglycan had occurred; this was consistent with the association of these two types with mental retardation. In the patients with MPS I S, no intracranial abnormalities were detected on MR images. MR imaging of the brain may be used to obtain a differential diagnosis of the various types of MPS, to estimate the extent of mental retardation, and to monitor the progress of this disease.

摘要

对8例黏多糖贮积症(MPS)患者进行了脑部磁共振成像(MR)检查。其中2例为MPS I S型,1例为MPS IIA型,2例为MPS IIB型,2例为MPS IIIB型,1例为MPS VI型。在MPS IIA型和MPS VI型患者中,脑白质的各个区域T1和T2时间延长。这些发现似乎与MPS病理变化的发展相对应,如在固定脑切片上观察到的白质血管周围凹陷。在MPS IIA型和MPS IIIB型患者中,白质未显示出正常的信号强度,这表明髓鞘形成不足,且已发生糖胺聚糖的浸润或沉积;这与这两种类型与智力发育迟缓的关联一致。在MPS I S型患者中,MR图像上未检测到颅内异常。脑部MR成像可用于对各种类型的MPS进行鉴别诊断,评估智力发育迟缓的程度,并监测该疾病的进展。

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The mucopolysaccharidoses: characterization by cranial MR imaging.
AJNR Am J Neuroradiol. 1993 Nov-Dec;14(6):1285-92.

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