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病例报告:吡喹酮治疗失败后,手术成功治疗难治性癫痫-脑裂头蚴病背后的移动性肿瘤样病灶

Case Report: Moving Tumor-Like Foci Behind Refractory Epilepsy-Cerebral Sparganosis Successfully Treated by Surgery After Failure of Praziquantel Treatment.

作者信息

Chen Yusi, Chen Xu, Kang Huicong

机构信息

Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Neurol. 2022 Feb 10;13:838849. doi: 10.3389/fneur.2022.838849. eCollection 2022.

Abstract

Cerebral sparganosis is clinically non-specific and easily misdiagnosed, exposing patients to the risk of severe brain damage and neurological dysfunction caused by actively migrating larvae. Diagnostic biomarkers from typical cases can help to establish an early diagnosis and proper treatment. We present a 25-year-old woman who suffered from 9 years of refractory epilepsy and was misdiagnosed with glioma and subjected to surgery. The postoperative pathology confirmed granuloma, and the tumor-like foci reappeared 3 months later. Along with the "tunnel sign" on MRI, cerebral sparganosis was suspected and confirmed by positive serum and cerebrospinal fluid antibodies against . The patient visited us after a failure of four cycles of praziquantel treatment, recurrent seizures and hemiplegia with basal ganglia foci. Craniotomy was not carried out until the larva moved to the superficial lobe on follow-up MRIs, and pathology revealed sparganosis granuloma. The patient became seizure-free and recovered myodynamia but had long-lasting cognitive dysfunction due to severe brain damage. This case indicated the importance of tunnel signs and moving tumor-like foci on MRI as diagnostic clues of cerebral sparganosis. An early diagnosis is vitally important to avoid severe neural dysfunction by the long-living and moving larvae. Surgical removal of the larva is a critical remedy for cases failed by praziquantel treatment.

摘要

脑裂头蚴病临床表现缺乏特异性,易被误诊,使患者面临因幼虫活跃移行导致严重脑损伤和神经功能障碍的风险。来自典型病例的诊断生物标志物有助于早期诊断和恰当治疗。我们报告一名25岁女性,患有9年难治性癫痫,曾被误诊为胶质瘤并接受手术。术后病理证实为肉芽肿,3个月后肿瘤样病灶再次出现。结合MRI上的“隧道征”,怀疑为脑裂头蚴病,并通过血清和脑脊液抗 抗体阳性得以确诊。该患者在吡喹酮治疗4个周期失败、癫痫复发且基底节区病灶出现偏瘫后前来就诊。直到随访MRI显示幼虫移至浅表叶才进行开颅手术,病理显示为裂头蚴病肉芽肿。患者癫痫发作停止,肌力恢复,但由于严重脑损伤出现了长期认知功能障碍。该病例表明MRI上的隧道征和移动的肿瘤样病灶作为脑裂头蚴病诊断线索的重要性。早期诊断对于避免长寿且移动的幼虫导致严重神经功能障碍至关重要。手术摘除幼虫是吡喹酮治疗失败病例的关键治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a760/8866191/ab3c72d4f35f/fneur-13-838849-g0001.jpg

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