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2-氯脱氧腺苷治疗巨大淋巴结增生症。

2-Chloro-deoxyadenosine therapy for giant lymph node hyperplasia.

作者信息

Bordeleau L, Bredeson C, Markman S

机构信息

Division of Haematology, University of Ottawa, Ontario, Canada.

出版信息

Br J Haematol. 1995 Nov;91(3):668-70. doi: 10.1111/j.1365-2141.1995.tb05366.x.

Abstract

Giant lymph node hyperplasia (GLNH) or Castleman disease is a heterogenous group of atypical lymphoproliferative disorders. Two main histologic variants, the hyaline vascular variant and the plasma cell variant, have been recognized. Although localized GLNH can often be managed successfully with surgery, optimal therapy for multifocal disease has yet to be identified. We report two cases of GLNH treated with 2-chloro-deoxyadenosine (2-CDA), a synthetic purine analogue. 2-CDA was utilized based on its relative lymphocytic toxicity and the putative pathophysiologic process in GLNH being either hamartomatous overgrowth (hyaline-vascular variant) or immune dysfunction and lymphoproliferation (plasma cell variant). One patient with unresectable localized hyaline-vascular GLNH has had a 9-month continuous complete remission following two courses of 2-CDA therapy followed by radiation therapy. The second patient with disseminated plasma cell type had a partial response to two cycles of 2-CDA therapy; however, further cycles were not given due to development of possible early neurotoxicity. Although the optimal management of non-resectable GLNH is yet to be determined, 2-CDA appears to be a viable therapeutic option for patients with this disease process.

摘要

巨大淋巴结增生症(GLNH)或卡斯尔曼病是一组异质性的非典型淋巴增生性疾病。已识别出两种主要的组织学变体,即透明血管变体和浆细胞变体。尽管局限性GLNH通常可通过手术成功治疗,但多灶性疾病的最佳治疗方法尚未确定。我们报告了两例用2-氯脱氧腺苷(2-CDA)治疗的GLNH病例,2-CDA是一种合成嘌呤类似物。使用2-CDA是基于其相对淋巴细胞毒性以及GLNH中假定的病理生理过程,即错构瘤性过度生长(透明血管变体)或免疫功能障碍和淋巴增生(浆细胞变体)。一名患有不可切除的局限性透明血管型GLNH的患者在接受两个疗程的2-CDA治疗后再进行放射治疗,已持续完全缓解9个月。第二名患有播散性浆细胞型的患者对两个周期的2-CDA治疗有部分反应;然而,由于可能出现早期神经毒性,未进行进一步的周期治疗。尽管不可切除的GLNH的最佳治疗方法尚未确定,但2-CDA似乎是患有这种疾病的患者的一种可行治疗选择。

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