Winkel M, Pagano M A, Allievi A, Kartin D, Lera G
División de Clínica Médica B y Unidad de Neurología, Hospital Juan A. Fernández, Buenos Aires, Argentina.
Neurologia. 1998 May;13(5):250-3.
Brainstem tuberculoma is exceptionally observed. We report a 44 year-old immunocompetent man with proven diagnosis of miliary tuberculosis (TBC) who developed a complex neurological syndrome characterized by right ophtalmoplegia, left-sided hemiparesis and hemihypoesthesia and a gross ipsilateral postural and action tremor with hand dystonia. A ponto-mesencephalic mass was detected by CT and MRI studies of the brain. Clinical, bacteriological and neuroimaging studies allowed to suspect a ponto-mesencephalic tuberculoma. Long-term therapy with anti-TBC drugs and steroids was started, achieving clinical and imaging improvement which retrospectively confirmed the diagnosis. Although with less amplitude, tremor persisted but a complete disappearance of focal dystonia was observed. The pathogenesis of both abnormal movements is particularly discussed since hand dystonia has never been mentioned in the literature as a consequence of brainstem damage.
脑干结核瘤极为罕见。我们报告一名44岁免疫功能正常的男性,确诊为粟粒性肺结核,出现了一种复杂的神经综合征,其特征为右眼眼肌麻痹、左侧偏瘫和偏身感觉减退,以及同侧明显的姿势性和动作性震颤伴手部肌张力障碍。脑部CT和MRI检查发现桥脑-中脑有一肿块。临床、细菌学和神经影像学检查怀疑为桥脑-中脑结核瘤。开始使用抗结核药物和类固醇进行长期治疗,临床和影像学均有改善,这在回顾性分析中证实了诊断。尽管震颤幅度减小,但仍持续存在,而局灶性肌张力障碍完全消失。本文特别讨论了这两种异常运动的发病机制,因为文献中从未提及脑干损伤会导致手部肌张力障碍。