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用Janus激酶抑制剂托法替布成功治疗的溃疡性结肠炎合并特发性血小板减少性紫癜难治性病例:一例报告

Refractory case of ulcerative colitis with idiopathic thrombocytopenic purpura successfully treated by Janus kinase inhibitor tofacitinib: A case report.

作者信息

Komeda Yoriaki, Sakurai Toshiharu, Sakai Kazuko, Morita Yasuyoshi, Hashimoto Arito, Nagai Tomoyuki, Hagiwara Satoru, Matsumura Itaru, Nishio Kazuto, Kudo Masatoshi

机构信息

Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka 589-8511, Japan.

Department of Genome Biology, Kindai University Faculty of Medicine, Osaka 589-8511, Japan.

出版信息

World J Clin Cases. 2020 Dec 26;8(24):6389-6395. doi: 10.12998/wjcc.v8.i24.6389.

Abstract

BACKGROUND

Concomitant ulcerative colitis (UC) and idiopathic thrombocytopenic purpura (ITP) is a rare phenomenon. The management of UC with ITP can be challenging, since a decreased platelet count augments UC.

CASE SUMMARY

A 24-year-old man with UC and steroid-resistant ITP experienced UC flare. Although continuous infusion of cyclosporine was initiated, UC did not improve. The administration of tofacitinib subsequently led to the induction of remission. The patient has maintained remission of UC and ITP for over one year on tofacitinib treatment. Whole transcriptomic sequencing was performed for inflamed rectal mucosae obtained before and after the initiation of Janus kinase (JAK) inhibitor, suggesting that distinct molecular signatures seemed to be regulated by JAK inhibitors and other conventional therapies including tumor necrosis factor lockers.

CONCLUSION

Tofacitinib should be considered in refractory cases of UC with ITP.

摘要

背景

溃疡性结肠炎(UC)与特发性血小板减少性紫癜(ITP)并存是一种罕见现象。UC合并ITP的治疗具有挑战性,因为血小板计数降低会加重UC。

病例摘要

一名患有UC且对类固醇耐药的ITP的24岁男性经历了UC发作。尽管开始持续输注环孢素,但UC并未改善。随后使用托法替布导致病情缓解。该患者在托法替布治疗下已维持UC和ITP缓解超过一年。对开始使用Janus激酶(JAK)抑制剂前后获取的发炎直肠黏膜进行了全转录组测序,表明不同的分子特征似乎受JAK抑制剂和包括肿瘤坏死因子阻滞剂在内的其他传统疗法调控。

结论

对于难治性UC合并ITP病例应考虑使用托法替布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b913/7760419/aa67dfb8bce5/WJCC-8-6389-g001.jpg

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