Ibrahim Ismail Ismail, K John John, Ibrahim Mohamed, Al-Hashel Jasem Yousef
Department of Neurology, Ibn Sina Hospital, Safat, Kuwait.
Department of Medicine, Faculty of Medicine, Health Sciences Centre, Kuwait University, Kuwait City, Kuwait.
Case Rep Neurol. 2020 Feb 5;12(1):50-55. doi: 10.1159/000505232. eCollection 2020 Jan-Apr.
Paraneoplastic neurological syndromes (PNS) associated with anti-CV2/CRMP5 antibodies are rare in the literature. Various clinical manifestations can occur including paraneoplastic limbic encephalitis (PLE). Thymoma is one of the rare causes that can be associated with this syndrome. It has not been reported in the literature in children or adolescents to the best of our knowledge. We report a case of PLE in a 19-year-old male patient secondary to thymoma that was diagnosed after 5 years of onset. Anti-CV2/CRMP5 antibodies were positive in the serum and became negative after thymectomy. Diagnosis of PNS should be evoked in cases with atypical neurological manifestation and can be confirmed by the presence of onconeuronal antibodies. We report the first pediatric PLE secondary to thymoma associated with anti-CV2/CRMP5 antibodies.
与抗CV2/CRMP5抗体相关的副肿瘤性神经系统综合征(PNS)在文献中较为罕见。可出现多种临床表现,包括副肿瘤性边缘叶脑炎(PLE)。胸腺瘤是可与此综合征相关的罕见病因之一。据我们所知,儿童或青少年中尚未见相关文献报道。我们报告一例19岁男性患者,继发于胸腺瘤的PLE,发病5年后确诊。血清中抗CV2/CRMP5抗体呈阳性,胸腺切除术后转为阴性。对于有非典型神经表现的病例应考虑PNS的诊断,可通过存在肿瘤神经元抗体来确诊。我们报告了首例继发于胸腺瘤且与抗CV2/CRMP5抗体相关的儿童PLE。