Pyoderma gangrenosum in ulcerative colitis patient treated with vedolizumab: adsorptive granulocyte/monocyte apheresis as a new therapeutic option refractory cases - a case report and literature review.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-11-03 eCollection Date: 2023-01-01 DOI:10.1177/20406223231194190
Mauro Mastronardi, Elisabetta Cavalcanti, Nunzia Labarile, Raffaele Armentano, Francesco Gabriele, Margherita Curlo
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Abstract

Extraintestinal manifestations occur rather frequently in ulcerative colitis (UC) and Crohn's disease patients and are usually related to an exacerbation of the underlying intestinal bowel disease but sometimes may run a course independent of the inflammatory bowel diseases (IBD). About one-third of patients with IBD develop extraintestinal manifestations, such as pyoderma gangrenosum (PG). PG is an uncommon inflammatory skin disorder of unknown pathogenesis. There are no specific serological or histological markers, and diagnosis is predominantly clinical. Topical and systemic therapies are both vital aspects of treatment and immune modulators have been used with increasing success in recent years, although immunosuppressive drugs raise some concerns due to an increased risk of serious and opportunistic infections and cancer, particularly in elderly and comorbid patients, underlining the unmet need for safer alternative therapies. Thus, in this case report, we highlighted an adsorptive granulocyte/monocyte apheresis (GMA) as a new therapeutic possibility in IBD patients with extraintestinal manifestations. We report a case of a 60-year woman with a history of UC with a Mayo grade 3 score which was associated with a PG. Given that the patients maintained clinical remission with vedolizumab, we preferred not to perform a combined treatment with other antitumor necrosis factor-alpha or ciclosporin, thus avoiding an increased risk of serious infections in the patient. Therefore, we performed the extracorporeal leukocyte apheresis. The patient progressed favorably, with progressive improvement of skin and bowel disease. Therefore, adsorptive GMA has a very favorable safety profile and has been confirmed in numerous studies. In this study, we underlined that an intensive regimen of GMA paves the way to an ideal option for patients with severe and refractory PG complicated with UC.

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vedolizumab治疗溃疡性结肠炎患者的坏疽性脓皮病:吸附性粒细胞/单核细胞单采作为一种新的治疗选择-难治性病例-病例报告和文献综述。
溃疡性结肠炎(UC)和克罗恩病患者的肠外表现相当频繁,通常与潜在肠道疾病的恶化有关,但有时可能独立于炎症性肠病(IBD)。大约三分之一的IBD患者出现肠外表现,如坏疽性脓皮病(PG)。PG是一种罕见的炎症性皮肤病,发病机制不明。没有特定的血清学或组织学标志物,诊断主要是临床诊断。局部和全身治疗都是治疗的重要方面,近年来免疫调节剂的使用越来越成功,尽管免疫抑制药物由于严重和机会性感染和癌症的风险增加而引起了一些担忧,尤其是在老年和合并症患者中,这突出了对更安全的替代疗法的需求未得到满足。因此,在本病例报告中,我们强调了吸附性粒细胞/单核细胞单采(GMA)作为一种新的治疗肠道外表现IBD患者的可能性。我们报告了一例有UC病史的60岁女性病例,其Mayo评分为3级,与PG相关。鉴于患者使用维多利珠单抗保持临床缓解,我们建议不要与其他抗肿瘤坏死因子α或环孢素联合治疗,从而避免患者严重感染的风险增加。因此,我们进行了体外白细胞单采。患者进展顺利,皮肤和肠道疾病逐渐好转。因此,吸附GMA具有非常有利的安全性,并已在大量研究中得到证实。在这项研究中,我们强调,GMA强化方案为重症和难治性PG合并UC患者的理想选择铺平了道路。
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4.30%
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567
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