Koh Sophie Jia Qian, Lo Yu Tung, Nga Vincent Diong Weng
Neurosurgery, National University Hospital, Singapore, SGP.
Cureus. 2025 Jul 23;17(7):e88602. doi: 10.7759/cureus.88602. eCollection 2025 Jul.
Paroxysmal sympathetic hyperactivity (PSH) is a potentially life-threatening clinical syndrome characterized by sudden, episodic increases in sympathetic nervous system activity. While commonly described after traumatic brain injury, it is a rare and under-recognized complication of intracerebral hemorrhage (ICH). Diagnosis is challenging in the acute setting due to its nonspecific presentation and constellation of symptoms. The pathophysiology remains poorly understood, and no standardized diagnosis or treatment guidelines exist. We describe a case of a 50-year-old male patient with spontaneous pontine ICH who developed PSH within a week of admission, with hyperthermia, hypertension, tachycardia, and dystonic posturing. Despite multimodal therapy with bromocriptine, baclofen and clobazam, the patient developed complications of rhabdomyolysis likely from drug-refractory paroxysmal rigidity and acute kidney injury requiring dialysis. This case highlights the diagnostic and therapeutic challenges of PSH in neurocritical care, underscoring the necessity of heightened clinical suspicion, exclusion of mimics, and early individualized treatment to optimise outcomes.
阵发性交感神经过度兴奋(PSH)是一种潜在的危及生命的临床综合征,其特征为交感神经系统活动突然发作性增加。虽然通常在创伤性脑损伤后出现,但它是脑出血(ICH)一种罕见且未被充分认识的并发症。由于其非特异性表现和一系列症状,在急性期诊断具有挑战性。其病理生理学仍知之甚少,并且不存在标准化的诊断或治疗指南。我们描述了一例50岁男性患者,患有自发性脑桥脑出血,在入院一周内出现PSH,伴有高热、高血压、心动过速和张力障碍姿势。尽管使用溴隐亭、巴氯芬和氯巴占进行了多模式治疗,但患者仍出现了可能源于药物难治性阵发性强直的横纹肌溶解并发症以及需要透析的急性肾损伤。该病例突出了PSH在神经重症监护中的诊断和治疗挑战,强调了提高临床怀疑度、排除类似情况以及早期个体化治疗以优化预后的必要性。