Iampreechakul Prasert, Wangtanaphat Korrapakc, Angsusing Chonlada, Hangsapruek Sunisa, Lertbutsayanukul Punjama, Kiathirannon Nitat, Thammachantha Samasuk, Tanpun Adisak, Komonchan Surasak
Department of Neurosurgery, Neurological Institute of Thailand, Bangkok, Thailand.
Department of Neuroradiology, Neurological Institute of Thailand, Bangkok, Thailand.
Surg Neurol Int. 2025 May 16;16:189. doi: 10.25259/SNI_146_2025. eCollection 2025.
Central nervous system (CNS) sparganosis is an exceptionally rare parasitic infection caused by the larvae of species. Its migratory nature and nonspecific clinical presentation often lead to misdiagnosis, posing significant diagnostic and therapeutic challenges. While CNS involvement typically affects either the brain or spinal cord, disseminated cases involving both regions are exceedingly rare.
We report the case of a 34-year-old woman who initially presented with progressive low back pain and paraparesis. She was diagnosed with spinal sparganosis following surgical resection and histopathological confirmation. Despite an uneventful postoperative recovery, she developed progressive headaches 3 years later. Magnetic resonance imaging revealed intracranial lesions, and subsequent surgery confirmed sparganosis in the cisterna magna. One year after brain surgery and ventriculoperitoneal shunt placement, the patient experienced progressive headaches accompanied by confusion. Under the initial misdiagnosis of brain abscess, she was inadvertently treated with intravenous metronidazole for 2 months, resulting in symptomatic improvement. However, a review of imaging demonstrated extensive CNS involvement, including the supratentorial, infratentorial, and upper cervical regions. In addition, there was clear evidence of parasite migration through the cribriform plate into the frontal lobe, highlighting the disseminated and migratory nature of CNS sparganosis.
This case highlights the diagnostic complexity and disseminated nature of CNS sparganosis, underscoring the importance of early surgical intervention and histopathological confirmation. The unexpected clinical response to metronidazole raises the possibility of its adjunctive role in symptom modulation, although its antiparasitic efficacy remains unproven. Given the risk of asymptomatic dissemination and recurrence, long-term follow-up with serial imaging is essential. Clinicians should maintain a high index of suspicion for sparganosis in endemic regions to improve diagnostic accuracy and patient outcomes.
中枢神经系统(CNS)裂头蚴病是一种由裂头蚴属幼虫引起的极为罕见的寄生虫感染。其游走特性和非特异性临床表现常导致误诊,给诊断和治疗带来重大挑战。虽然中枢神经系统受累通常影响大脑或脊髓,但累及这两个区域的播散性病例极为罕见。
我们报告了一名34岁女性的病例,她最初表现为进行性下腰痛和双下肢轻瘫。手术切除及组织病理学确诊后,她被诊断为脊髓裂头蚴病。尽管术后恢复顺利,但3年后她出现了进行性头痛。磁共振成像显示颅内病变,随后的手术证实枕大池有裂头蚴病。在脑部手术和脑室腹腔分流术后一年,患者出现进行性头痛并伴有意识模糊。最初被误诊为脑脓肿,她无意中接受了2个月的静脉甲硝唑治疗,症状有所改善。然而,影像学复查显示中枢神经系统广泛受累,包括幕上、幕下和上颈椎区域。此外,有明确证据表明寄生虫通过筛板迁移至额叶,突出了中枢神经系统裂头蚴病的播散性和游走性。
该病例突出了中枢神经系统裂头蚴病的诊断复杂性和播散性,强调了早期手术干预和组织病理学确诊的重要性。甲硝唑意外的临床反应增加了其在症状调节中辅助作用的可能性,尽管其抗寄生虫疗效尚未得到证实。鉴于无症状播散和复发的风险,定期影像学检查的长期随访至关重要。在流行地区,临床医生应高度怀疑裂头蚴病,以提高诊断准确性和患者预后。