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真性红细胞增多症所致脑梗死的延迟表现及缓慢进展

Delayed manifestation and slow progression of cerebral infarction caused by polycythemia rubra vera.

作者信息

Kurabayashi Hitoshi, Hishinuma Akiko, Uchida Ryusei, Makita Shigeru, Majima Mitsuru

机构信息

Department of Rehabilitation Medicine, Saitama Medical University, Moroyama, Japan.

出版信息

Am J Med Sci. 2007 May;333(5):317-20. doi: 10.1097/MAJ.0b013e31805370a9.

Abstract

BACKGROUND

Polycythemia rubra vera is often found after the manifestation of cerebral infarction, though the pathogenesis is still controversial. We present a case of cerebral infarction secondary to polycythemia rubra vera, which presented a slow expansion on magnetic resonance imaging despite severe hemiplegia. This case suggests a possible mechanism for development of cerebral infarction in polycythemia rubra vera.

METHODS

This case report was conducted in a university hospital. Magnetic resonance imaging and diffusion-weighted imaging were performed to assess the evolution of infarction, and the total blood volume and cerebral blood flow were determined with the use of isotopes, Cr and Tc, respectively. Phlebotomy was performed, but intervention was not applicable. The manual muscle test and sensory disturbance were assessed by the same physiotherapist throughout the clinical course.

RESULTS

A 64-year-old male patient with polycythemia rubra vera had a cerebral infarction. A subtle change was observed on CT scan on the third day after the onset of infarction, and a small signal was demonstrated on magnetic resonance imaging on the fourth day. The cerebral infarction expanded slowly in size and reached a maximum on day 24. A diagnosis of cerebral infarction secondary to polycythemia rubra vera was made, and treatment by phlebotomy, hydration, and hydroxyurea was begun. Though the hemiplegia remained, he became ambulatory with a brace, as do patients with atherosclerotic infarction.

CONCLUSIONS

It is suggested that the delayed manifestation and slow expansion of cerebral infarction caused by elevated hematocrit might be derived from a pathogenesis different from atherosclerotic infarction.

摘要

背景

真性红细胞增多症常在脑梗死症状出现后被发现,但其发病机制仍存在争议。我们报告一例由真性红细胞增多症继发的脑梗死病例,该病例在磁共振成像上显示梗死灶缓慢扩大,尽管患者有严重偏瘫。该病例提示了真性红细胞增多症中脑梗死发生发展的一种可能机制。

方法

本病例报告在一家大学医院进行。采用磁共振成像和扩散加权成像评估梗死灶的演变,分别使用同位素铬(Cr)和锝(Tc)测定全血容量和脑血流量。进行了放血治疗,但未采取其他干预措施。在整个临床过程中,由同一名物理治疗师评估徒手肌力测试和感觉障碍情况。

结果

一名64岁患真性红细胞增多症的男性患者发生了脑梗死。梗死发作后第三天的CT扫描观察到细微变化,第四天的磁共振成像显示有小信号。脑梗死灶大小缓慢扩大,在第24天达到最大。诊断为真性红细胞增多症继发的脑梗死,并开始采用放血、补液和羟基脲治疗。尽管偏瘫仍然存在,但他像患动脉粥样硬化性梗死的患者一样,借助支具能够行走。

结论

提示血细胞比容升高导致的脑梗死延迟表现和缓慢扩大可能源于与动脉粥样硬化性梗死不同的发病机制。

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