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Clinical Features end Outcome in Seven Patients with Hyaline or Mixed Variant Type of Castleman's Disease. A Single Center Experience

机译：临床特征在透明或混合变种类型的Castleman疾病中的七名患者结束。单一中心经验

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Castleman's Disease (CD) is a rare lymphoproliferative disease of unknow origin that belongs to so-called atypical lymphoproliferative disorders. Here we report seven new cases with a histologic diagnosis of CD hyaline-vascular (4/7) or mixed (3/7) variant type. Five patients had localized disease. Complete remission was obtained in 6/7 cases (86%). The median follow-up is 50 months. All patients are currently alive, only one with disease (partial remission). The favourable outcome of these cases confirme that surgery is treatment of choice for localized CD especially on the hyaline-vascular histologic type.

机译：Castleman的疾病（CD）是一种罕见的淋巴抑制性疾病，属于所谓的非典型淋巴抑制性疾病。在这里，我们报告了七种新病例，其组织学诊断CD透明血管（4/7）或混合（3/7）变体类型。五名患者有局部疾病。在6/7例（86％）中获得完全缓解。中位后续时间为50个月。所有患者目前都是活着的，只有一种疾病（部分缓解）。这些病例的有利结果证实，手术是治疗局部CD的选择，特别是在透明血管组织学类型上。

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《European Haematology Association》|2002年||共4页
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A. Candoni; D. Damiani; R. Fanin;
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正文语种
中图分类血液疾病;
关键词
Castleman's disease; Atypical lymphoproliferative disorders.;

机译：Castleman的疾病;非典型淋巴抑制剂疾病。;

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Clinical Features end Outcome in Seven Patients with Hyaline or Mixed Variant Type of Castleman's Disease. A Single Center Experience

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