Hamaji Masatsugu, Neal Joel W, Burt Bryan M
Department of Thoracic Surgery, Kyoto University, Kyoto, Japan.
Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Ann Thorac Surg. 2015 Jan;99(1):e7-9. doi: 10.1016/j.athoracsur.2014.10.028.
A 30-year-old man presented with rapidly progressive cerebellar symptoms. Brain magnetic resonance imaging was consistent with cerebellitis. A subsequent chest computed tomography revealed a multilobulated anterior mediastinal mass, which was diagnosed on the surgical biopsy specimen as hyaline vascular Castleman disease. After resection of the mediastinal mass and multiple involved adjacent mediastinal lymph nodes, the cerebellitis resolved. To the best of our knowledge, this is the first report of Castleman disease associated with cerebellitis. This rare case of suspected paraneoplastic cerebellitis related to a multifocal unicentric Castleman disease confined to the mediastinum is discussed.
一名30岁男性出现快速进展的小脑症状。脑部磁共振成像与小脑炎相符。随后的胸部计算机断层扫描显示前纵隔有一个分叶状肿块,手术活检标本诊断为透明血管型Castleman病。切除纵隔肿块及多个受累的相邻纵隔淋巴结后,小脑炎症状缓解。据我们所知,这是Castleman病合并小脑炎的首例报告。本文讨论了这例罕见的疑似与局限于纵隔的多灶性单中心Castleman病相关的副肿瘤性小脑炎病例。