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Review: Emerging role of thalidomide in the treatment of gastrointestinal bleeding

机译:综述:沙利度胺在胃肠道出血治疗中的新兴作用

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摘要

Thalidomide was initially synthesised in 1954 and marketed as a sedative and antiemetic for morning sickness. It was withdrawn in 1961 due to the realisation that it was teratogenic with over 10 000 children born with congenital abnormalities. Since then it has been used for treatment of dermatological and oncological conditions, including myeloma. In 1994, it was found to have a potent antiangiogenic effect via downregulation of vascular endothelial growth factor (VEGF). This has led to its use in gastrointestinal bleeding, as vascular abnormalities such as angiodysplasia have been found to have elevated VEGF levels. This article will review the current evidence of the use of thalidomide in bleeding associated with gastrointestinal vascular malformations, including angiodysplasia, gastric cancer and radiation-induced proctitis.
机译:沙利度胺最初于1954年合成,并作为镇静和止吐药用于晨吐。由于认识到它具有致畸性,有超过1万名先天性畸形的儿童而于1961年被撤回。从那时起,它已被用于治疗皮肤病和肿瘤病,包括骨髓瘤。 1994年,发现它通过下调血管内皮生长因子(VEGF)具有有效的抗血管生成作用。由于发现血管异常(例如血管增生)的VEGF水平升高,因此已将其用于胃肠道出血。本文将回顾使用沙利度胺治疗与胃肠道血管畸形(包括血管增生,胃癌和放射性诱发的直肠炎)相关的出血的最新证据。

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