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川崎病患者的区域性脑血流异常。

Regional cerebral blood flow abnormalities in patients with kawasaki disease.

机构信息

Department of Pediatrics, Teikyo University School of Medicine, Itabashi-Ku, Tokyo, Japan.

出版信息

Clin Nucl Med. 2011 Aug;36(8):643-9. doi: 10.1097/RLU.0b013e318217adfc.

DOI:10.1097/RLU.0b013e318217adfc
PMID:21716013
Abstract

PURPOSE

Kawasaki disease (KD) is an acute febrile disorder of unknown etiology. Brain single-photon emission computed tomography (SPECT) and magnetic resonance imaging (MRI) help in detecting regional cerebral blood flow abnormalities and brain damage. The usefulness of SPECT and MRI in patients with KD was evaluated.

MATERIALS AND METHODS

All 22 patients with KD underwent brain SPECT using Tc-99m-hexamethyl propylene amine oxime from 6 days to 3 years after onset, and 8 patients underwent brain MRI. Of the 22 patients, 4 had neurologic symptoms. Case 1 showed prolonged apnea; case 2, prolonged disturbance of consciousness; and cases 3 and 4 generalized tonic-clonic seizures. Initial brain SPECT showed localized hypoperfusion in 4 and 13 patients with and without neurologic symptoms, respectively.

RESULTS

All patients with neurologic symptoms underwent follow-up SPECT; localized hypoperfusion was detected between 1- and 6-month follow-up in 3 of these patients. Six patients without neurologic symptoms underwent follow-up SPECT. Localized hypoperfusion was detected at approximately 1- to 11-month follow-up in 4 of these patients. Diffusion-weighted imaging revealed abnormal high-intensity areas in the corpus callosum in case 1. Case 2 showed a bilateral chronic subdural hematoma with decreased size and ischemic changes, and case 3 showed bilateral hippocampal atrophy and left hippocampal sclerosis.

CONCLUSIONS

Because the occurrence of localized hypoperfusion is possibly not restricted to only the acute phase in KD, brain SPECT and MRI should also be performed in KD patients with neurologic symptoms.

摘要

目的

川崎病(KD)是一种病因不明的急性发热性疾病。脑单光子发射计算机断层扫描(SPECT)和磁共振成像(MRI)有助于检测区域性脑血流异常和脑损伤。评估了 SPECT 和 MRI 在 KD 患者中的作用。

材料和方法

所有 22 例 KD 患者在发病后 6 天至 3 年内均接受 Tc-99m-六甲基丙烯酰胺肟脑 SPECT 检查,8 例患者接受脑 MRI 检查。22 例患者中,有 4 例有神经系统症状。例 1 表现为长时间呼吸暂停;例 2 ,长时间意识障碍;例 3 和例 4 全身性强直阵挛发作。4 例和 13 例有和无神经系统症状的患者分别在初始脑 SPECT 上显示局部灌注不足。

结果

所有有神经系统症状的患者均进行了随访 SPECT;其中 3 例在 1-6 个月随访时发现局部灌注不足。6 例无神经系统症状的患者进行了随访 SPECT。其中 4 例在 1-11 个月随访时发现局部灌注不足。弥散加权成像显示例 1 胼胝体异常高信号区。例 2 表现为双侧慢性硬膜下血肿,体积减小,伴有缺血性改变,例 3 表现为双侧海马萎缩和左侧海马硬化。

结论

由于局部灌注不足的发生可能不仅限于 KD 的急性期,因此也应在 KD 伴有神经系统症状的患者中进行脑 SPECT 和 MRI 检查。

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