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一种非典型的华氏巨球蛋白血症,经多次化疗后完全缓解持续两年以上(作者译)

[An atypical form of Waldenstrom's macroglobulinaemia with complete remission lasting for more than two years after multiple chemotherapy (author's transl)].

作者信息

Bierling P, Rochant H, Brun B, Intrator L, Dreyfus B

出版信息

Ann Med Interne (Paris). 1979;130(10):443-7.

PMID:119455
Abstract

An authentic case of Waldenstrom's macroglobulinaemia without a tumoural syndrome is reported, with initial signs of peripheral pancytopenia. Complete and persistent remission appears to have followed multiple sequential chemotherapy. This very satisfactory and, according to data in the published literature, very rare result suggests that this type of treatment should be prescribed for all patients with macroglobulinaemia with poor prognostic clinical and histological characteristics.

摘要

报告了一例无肿瘤综合征的华氏巨球蛋白血症真实病例,最初表现为外周血细胞减少。多次序贯化疗后出现完全且持久的缓解。这一非常令人满意且根据已发表文献数据非常罕见的结果表明,对于所有具有预后不良临床和组织学特征的巨球蛋白血症患者均应采用这种治疗方法。

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