Gianaris P G, Leestma J E, Cerullo L J, Butler A
Department of Surgery, Northwestern University Medical School, Chicago, Illinois.
Neurosurgery. 1989 Apr;24(4):608-13. doi: 10.1227/00006123-198904000-00021.
Castleman's disease is an uncommon lymphoproliferative disorder that manifests itself as a local or generalized tumor-like condition affecting both lymph nodes and nonnodal tissues, usually in the chest or abdomen. Only two prior examples involving the central nervous system had been reported when this patient was encountered. Very recently, three additional cases have been reported by Severson et al. We report the sixth case of Castleman's disease affecting the central nervous system, which occurred in a 63-year-old woman in whom the diagnosis was made after craniotomy for a mass lesion involving the dura over the frontal regions. Neuroradiological, clinical, and immunopathological characteristics of the case are presented. The lesion was treated with cranial irradiation and the patient is alive and symptom free three years after initial treatment.
卡斯特尔曼病是一种罕见的淋巴增生性疾病,表现为局部或全身性肿瘤样病变,可累及淋巴结和非淋巴结组织,通常位于胸部或腹部。在遇到该患者时,此前仅报道过两例累及中枢神经系统的病例。最近,塞弗森等人又报道了另外三例。我们报告第六例累及中枢神经系统的卡斯特尔曼病,该病例发生在一名63岁女性身上,她因额叶硬脑膜肿块病变接受开颅手术后确诊。本文介绍了该病例的神经放射学、临床和免疫病理学特征。病变接受了头部放疗,患者在初始治疗三年后仍存活且无症状。