Feenstra Froukje A, Aggenbach Laura, Rijtema Gijs, Buunk Anne M, Stirler Vincent M A
UMCG, Afd. Chirurgie, Groningen.
Contact: Froukje A. Feenstra (
Ned Tijdschr Geneeskd. 2020 Feb 17;164:D4397.
Bálint's syndrome is characterized by the triad of ocular apraxia, dorsal simultanagnosia and optic ataxia. It most commonly occurs following bilateral parieto-occipital brain injury, for which several aetiologies have been described.
We present a case of a 39-year-old male with penetrating brain injury following a suicide attempt with a crossbow. A CT scan of the head revealed the intracranial position of the arrow, piercing the parietal and occipital cortex from the left-parietal direction with the tip on the right parietal bone. After surgical removal of the arrow, visuospatial symptoms persisted that were consistent with Bálint's syndrome. The characteristic symptoms, patho-anatomy and treatment of this syndrome are discussed in this article.
The patient in this case had visual impairment following a suicide attempt with a crossbow. On the basis of neurological and neuropsychological assessments, the triad of ocular apraxia, dorsal simultanagnosia and optic ataxia was observed, characteristic of Bálint's syndrome.
巴林特综合征的特征为眼球失用、背侧同时失认和视觉性共济失调三联征。它最常发生于双侧顶枕部脑损伤后,对此已有多种病因描述。
我们报告一例39岁男性,其在试图用弩自杀后发生穿透性脑损伤。头部CT扫描显示箭头在颅内的位置,箭头从左顶叶方向刺入顶叶和枕叶皮质,尖端位于右侧顶骨。手术取出箭头后,持续存在与巴林特综合征相符的视觉空间症状。本文讨论了该综合征的特征性症状、病理解剖及治疗。
该病例患者在用弩自杀后出现视力障碍。基于神经学和神经心理学评估,观察到眼球失用、背侧同时失认和视觉性共济失调三联征,这是巴林特综合征的特征。