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[1例斯图尔特-特里夫斯综合征——重组白细胞介素2治疗及日本文献综述]

[A case of Stewart-Treves syndrome--treatment with recombinant interleukin 2 and a review of Japanese literature].

作者信息

Nabeya R, Kobayashi M, Fujita M, Yorifuji K, Eguchi N, Okamoto S

机构信息

Department of Dermatology, Chiba University School of Medicine.

出版信息

Nihon Hifuka Gakkai Zasshi. 1990 Sep;100(10):1029-39.

PMID:2266596
Abstract

A 76-year-old woman developed angiosarcoma 11 years after a radical mastectomy in the chronic lymphedema of the ipsilateral arm, referred to as Stewart-Treves syndrome. The patient was treated by intravenous and intralesional injection of recombinant interleukin 2 (rIL-2; TGP-3, Takeda Chemical Industries, LTD, Osaka). Intralesional injection was more effective than systemic administration. After a month, the lesion where the local injection was done showed little tumor cells with a dense infiltrate composed of lymphoid cells. It was observed that NK activity, LAK activity and IL-2 receptor positive T-cells in the peripheral blood increased during the administration of rIL-2. As the lesion was too large to be treated with rIL-2 alone, radiotherapy was performed. But the patient had no remarkably improvement and died 16 months later from the onset. Immunotherapy with rIL-2 can be useful for angiosarcoma and more effective regimen of rIL-2 is a important problem.

摘要

一名76岁女性在根治性乳房切除术后11年,于同侧手臂慢性淋巴水肿部位发生血管肉瘤,即所谓的斯图尔特-特雷夫斯综合征。患者接受了重组白细胞介素2(rIL-2;TGP-3,武田化学工业株式会社,大阪)的静脉注射和瘤内注射治疗。瘤内注射比全身给药更有效。一个月后,进行局部注射的病变部位肿瘤细胞很少,有由淋巴细胞组成的密集浸润。观察到在给予rIL-2期间外周血中的自然杀伤(NK)活性、淋巴因子激活的杀伤(LAK)活性和白细胞介素2受体阳性T细胞增加。由于病变太大,无法仅用rIL-2治疗,遂进行了放射治疗。但患者没有明显改善,发病16个月后死亡。rIL-2免疫疗法对血管肉瘤可能有用,更有效的rIL-2治疗方案是一个重要问题。

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