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Castleman病9例报道 被引量:2

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摘要 目的总结Castleman病的临床特征及诊治经验。方法回顾性分析2010年1月至2014年12月期间我院收治的9例Castleman病患者的临床资料。结果本组患者发病部位以颈部多见(4例),病理分型以透明血管型多见(5例),5例局灶型Castleman病患者经手术治疗取得良好效果;3例多中心型Castleman病患者经环磷酰胺+多柔比星+长春新碱+泼尼松(CHOP)化疗后病情得到好转,1例中心型Castleman病患者因基础疾病未化疗而复发。结论 Castleman病是一种罕见的淋巴系统增生性疾病,无特异性表现,诊断依赖于病理组织学,手术是治疗局灶型Castleman病的首选方法,CHOP化疗方案是治疗中心型Castleman病的一种有效方案。
出处 《中国普外基础与临床杂志》 CAS 2016年第2期234-236,共3页 Chinese Journal of Bases and Clinics In General Surgery
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参考文献9

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二级参考文献16

  • 1Hisaaki Miyoshi,Shima Mimura,Takako Nomura,Joji Tani,Asahiro Morishita,Hideki Kobara,Hirohito Mori,Hirohito Yoneyama,Akihiro Deguchi,Takashi Himoto,Naoki Yamamoto,Keiichi Okano,Yasuyuki Suzuki,Tsutomu Masaki.A rare case of hyaline-type Castleman disease in the liver[J].World Journal of Hepatology,2013,5(7):404-408. 被引量:14
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