Launay M, Bozzolo E, Venissac N, Delmont E, Fredenrich A, Thomas P
Service de neurologie, pavillon F, hôpital Pasteur, 30, voie Romaine, B.P. 69, 06002 Nice, France.
Rev Neurol (Paris). 2008 Jun-Jul;164(6-7):612-9. doi: 10.1016/j.neurol.2008.02.044. Epub 2008 May 13.
We report the case of a 49-year-old man who was admitted for progressive behaviorial disorders with frontal elements. There was no sensorial nor motor deficiency. Clinical examination revealed android obesity, cutaneous and mucous paleness, pubic and axillary depilation and gynecomastia. Encephalic MRI found a lesion of the left amygdalian region with high T2 intensity and low T1 intensity associated with gadolinium-enhancement. Cerebrospinal fluid analysis showed a lymphocytic meningitis. Panhypopituitarism was found on the endocrine investigations. Anti-RI antibodies were positive, leading to the diagnosis of paraneoplastic limbic encephalitis. The CT-scan showed a node of the lower part of the thymic area. Surgical resection revealed an ectopic mediastinal seminoma. The evolution consisted of paraneoplastic fever and crossed-syndrome with right hemiparesia and left common oculomotor nerve paralysis. Treatment was completed by two cycles of carboplatin, corticosteroids and substitutive opotherapy. Paraneoplastic fever disappeared, but behavioral disorders and palsy remain unchanged. The patient died two years later in a bedridden state. This case of paraneoplastic limbic encephalitis associated with positive anti-RI antibodies and mediastinal seminoma is exceptional and has not to our knowledge been described in the literature. Cancers usually associated with anti-RI antibody are breast and lung cancer. Paraneoplastic limbic encephalitis is not the classical clinical presentation, which usually is brainstem encephalitis. Hypothalamic involvement, uncommon in paraneoplastic limbic encephalitis is mainly associated with positive antineuronal anti-Ma2 antibodies. Finally, the gadolinium enhancement on encephalic MRI is unusual in paraneoplastic limbic encephalitis.
我们报告了一例49岁男性患者,因伴有额叶症状的进行性行为障碍入院。患者无感觉或运动功能缺陷。临床检查发现其呈男性化肥胖、皮肤和黏膜苍白、阴毛和腋毛脱落以及乳腺增生。脑部磁共振成像(MRI)发现左侧杏仁核区域有一个T2高信号、T1低信号且钆增强的病变。脑脊液分析显示为淋巴细胞性脑膜炎。内分泌检查发现全垂体功能减退。抗RI抗体呈阳性,从而诊断为副肿瘤性边缘叶脑炎。计算机断层扫描(CT)显示胸腺区域下部有一个结节。手术切除显示为纵隔异位精原细胞瘤。病情发展包括副肿瘤性发热以及出现交叉综合征,伴有右侧偏瘫和左侧动眼神经麻痹。通过两个周期的卡铂、皮质类固醇和替代疗法完成了治疗。副肿瘤性发热消失,但行为障碍和麻痹症状未改变。患者两年后卧床不起,最终死亡。这例与抗RI抗体阳性和纵隔精原细胞瘤相关的副肿瘤性边缘叶脑炎病例较为罕见,据我们所知,文献中尚未有过描述。通常与抗RI抗体相关的癌症是乳腺癌和肺癌。副肿瘤性边缘叶脑炎并非典型的临床表现,典型表现通常是脑干脑炎。下丘脑受累在副肿瘤性边缘叶脑炎中并不常见,主要与抗神经元抗Ma2抗体阳性有关。最后,脑部MRI上的钆增强在副肿瘤性边缘叶脑炎中并不常见。