Gerstmann Syndrome as a Disconnection Syndrome: A Single Case Diffusion Tensor Imaging Study.

Soo Hoon Yoon, Jae Ik Lee, Mun Jeong Kang, Hae In Lee, Sung-Bom Pyun
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Abstract

Gerstmann syndrome (GS) is a rare syndrome that occurs when there is a lesion of the dominant inferior parietal lobule (IPL), causing agraphia, acalculia, finger agnosia, and right-left disorientation. A 49-year-old right-handed male was diagnosed as GS after left parieto-occipital lobe hemorrhage. The patient showed mild anomic aphasia with agraphia in the language test and the neuropsychological test revealed acalculia, impaired right-left discrimination, and finger agnosia. In diffusion tensor tractography, the tracts of left superior longitudinal fasciculus (SLF), middle longitudinal fasciculus, U-fibers and posterior corpus callosum (CC) were disrupted around the left IPL. In addition, fractional anisotropy (FA) values were markedly decreased in left SLF, and posterior CC when compared to twelve healthy control subjects. Our clinical and neuroimaging findings support that GS is a disconnection syndrome caused by lesion in the white matter pathway surrounding IPL. In future, more studies of the correlation between the white matter disconnection and the development of GS including high quality imaging technique are needed.

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Gerstmann综合征作为一种断连综合征:一例弥散张量成像研究。
Gerstmann综合征(GS)是一种罕见的综合征,发生在显性下顶叶(IPL)病变时,可引起失写症、失算症、手指失认症和左右定向障碍。一位49岁的右撇子男性在左顶枕叶出血后被诊断为GS。患者语言测试表现为轻度失语症伴失写症,神经心理测试表现为失算、左右辨别障碍、手指失认。在弥散张量束造影中,左侧上纵束、中纵束、u -纤维束和后胼胝体束在左IPL周围被破坏。此外,与12名健康对照者相比,左侧SLF和后部CC的分数各向异性(FA)值显着降低。我们的临床和神经影像学结果支持GS是一种由IPL周围白质通路病变引起的断开综合征。未来需要更多的研究白质断开与GS发展的相关性,包括高质量的成像技术。
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