目的 探讨结肠系膜局限型Castleman病的临床病理特征。方法 回顾性分析发生在结肠系膜的Castleman病1例,并结合相关文献及免疫组织化学技术进行分析。结果 诊断Castleman病(透明血管型),系原发于乙状结肠肠系膜内。结论 原发于乙状结肠肠系膜局灶型Castleman病,较为罕见,施行肿块手术切除,预后好,随访2年10个月无复发。

Objective To investigate the clinical and pathological features of mesocolon localized Castleman's disease. Methods A retrospective analysis of 1 case of localized Castleman's disease, occurred in the mesocolon, and unifies the immunohistochemical technique and pertinent literature. Results The Castleman disease (hyaline vascular type) isdiagnosed primary sigmoid mesentery. Conclusion Primary sigmoid mesentery localized Castleman's disease is a rare tumor. After surgical resection, prognosis is good, followed up for 10 months without recurrence.