Ropponen K M, Kankkunen J P, Ronkainen A, Vihavainen M, Alafuzoff I
Department of Pathology, Kuopio University Hospital, Kuopio, Finland.
Clin Neuropathol. 2002 Nov-Dec;21(6):278-83.
Castleman's disease is an uncommon benign lymphoproliferative disorder that arises in lymph nodes. Few cases of Castleman's disease affecting the central nervous system have been described.
We report 2 new cases of Castleman's disease confined solely to the leptomeninges. The patients were referred to neurosurgery with presumptive clinical diagnosis of meningiomas. Histological investigation of the operative specimens taken from the abnormal leptomeninges revealed nodular lymphoid areas with multiple germinal centers surrounded by concentrically layered proliferations of small lymphocytes. Histologically, these 2 cases fulfilled the classification criteria for the mixed and for the hyaline-vascular type of Castleman's disease. The immunohistochemical analysis revealed a polyclonal B cell proliferation in the lesions with perifollicular T cell proliferation with the T helper cell predominance.
The authors conclude that Castleman's disease involving the leptomeninges have a similar immunological pattern reported for the disease in extracranial locations and that, though being rare, Castleman's disease should be considered as a differential diagnosis when dealing with mass lesions of leptomeninges.
卡斯特曼病是一种发生于淋巴结的罕见良性淋巴增生性疾病。很少有卡斯特曼病累及中枢神经系统的病例被描述。
我们报告2例仅局限于软脑膜的卡斯特曼病新病例。患者因临床疑似脑膜瘤被转诊至神经外科。对取自异常软脑膜的手术标本进行组织学检查,发现有多个生发中心的结节状淋巴样区域,周围是小淋巴细胞的同心层状增生。组织学上,这2例病例符合卡斯特曼病混合型和透明血管型的分类标准。免疫组化分析显示病变中有多克隆B细胞增殖,伴有滤泡周围T细胞增殖,且以辅助性T细胞为主。
作者得出结论,累及软脑膜的卡斯特曼病具有与颅外部位该疾病报道相似的免疫模式,并且,尽管罕见,但在处理软脑膜肿块病变时,卡斯特曼病应被视为鉴别诊断之一。