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皮内注射活化蛋白C用于治疗坏疽性脓皮病继发的大型慢性伤口。

Use of dermal injection of activated protein C for treatment of large chronic wounds secondary to pyoderma gangrenosum.

作者信息

Kapila S, Reid I, Dixit S, Fulcher G, March L, Jackson C, Cooper A

机构信息

Department of Dermatology, Kolling Institute of Medical Research, University of Sydney Royal North Shore Hospital, St Leonards, NSW, Australia.

出版信息

Clin Exp Dermatol. 2014 Oct;39(7):785-90. doi: 10.1111/ced.12361. Epub 2014 Aug 22.

DOI:10.1111/ced.12361
PMID:25155809
Abstract

BACKGROUND

Pyoderma gangrenosum (PG) is a systemic disease that presents with cutaneous necrotizing ulceration, producing deep necrotic ulcers, usually with a raised, undermined, violaceous border. Treatment typically involves high dose immunosuppressive drugs, but more recently anti-tumour necrosis factor and monoclonal antibodies have been used. Activated protein C (APC) stimulates wound healing in patients with treatment-refractory skin ulcers, possibly by stimulating angiogenesis and re-epithelialization, and preventing inflammation.

AIM

To investigate whether APC may be beneficial as a treatment for ulcers related to cutaneous PG.

METHODS

Two patients were recruited with a clinical history and physical and histopathological evidence of acute PG. A total of 400 μg (1.0 mL) of APC was injected subcutaneously into the dermal edge of necrotic PG ulcers weekly for a total treatment period of 6 weeks. Photographs were taken, and clinical progress, ulcer size and pain score were monitored during this period and after the cessation of treatment, at weeks 8 and 12.

RESULTS

Over the 12 weeks of the trial, APC led to a reduction in wound size from 3.8 cm(2) to 0.8 cm(2) in patient 1 (78.9% decrease) and from 41 cm(2) to 16 cm(2) in patient 2 (70.0% decrease, respectively), and a reduction in pain scores from 10 to 0 (100% decrease) in both patients.

CONCLUSION

Although this study has limited because of its small sample size and lack of a true placebo group, it does indicate that APC has potential as a therapeutic option for patients with chronic skin ulcers from PG.

摘要

背景

坏疽性脓皮病(PG)是一种全身性疾病,表现为皮肤坏死性溃疡,形成深部坏死性溃疡,通常边界隆起、呈潜行性、紫红色。治疗通常涉及高剂量免疫抑制药物,但最近也使用了抗肿瘤坏死因子和单克隆抗体。活化蛋白C(APC)可刺激治疗难治性皮肤溃疡患者的伤口愈合,可能是通过刺激血管生成和重新上皮化以及预防炎症来实现的。

目的

研究APC作为治疗与皮肤PG相关溃疡的药物是否有益。

方法

招募了两名有急性PG临床病史及体格检查和组织病理学证据的患者。将总共400μg(1.0mL)的APC每周皮下注射到坏死性PG溃疡的真皮边缘,共治疗6周。在此期间以及治疗停止后的第8周和第12周拍摄照片,并监测临床进展、溃疡大小和疼痛评分。

结果

在为期12周的试验中,APC使患者1的伤口大小从3.8cm²减小至0.8cm²(减少78.9%),患者2的伤口大小从41cm²减小至16cm²(分别减少70.0%),且两名患者的疼痛评分均从10降至0(降低100%)。

结论

尽管本研究因样本量小且缺乏真正的安慰剂组而存在局限性,但它确实表明APC有潜力成为PG慢性皮肤溃疡患者的一种治疗选择。

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