麻疹、腮腺炎和风疹疫苗免疫治疗传染性软疣的疗效:一项前瞻性研究

Fariz Sarshar, Mohammad Adil, Prateek Pathak, Triveni Harode, Mitali Sethi
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They were injected with the MMR vaccine intralesionally into 2-3 lesions including the largest mollusca up to a maximum of 0.3 ml in one sitting every 2 weeks for a maximum of 5 treatments at a 2-week interval (week: 0, 2, 4, 6, 8) or till the complete resolution of MC whichever was earlier. The action of the MMR vaccine was assessed by the reduction of the number of lesions and the day of resolution of lesions. The response of all patients at subsequent visits (at second, fourth, sixth, eighth, and 10th week from the initiation of therapy which was taken as week 0) was analyzed. All the patients were subjected to photographic documentation before the initiation of therapy, during therapy, and at 1 month (week 14) and 3 months (week-22) of the follow-up period. Results Out of 200 patients, 184 completed the study. There were 116 males and 84 females. The mean age of study participants was 17.17±12.64 years. 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引用次数: 0

摘要

传染性软疣(MC)是一种皮肤和粘膜的病毒感染,其特征是单个或多个,珍珠白色到肉色的脐丘疹。由于细胞介导的免疫在MC的消退中起着重要的作用,有一些特定的治疗方法可以通过局部或全身的方式增加细胞免疫反应。免疫调节药物是相对较新的治疗方式,对于广泛的和可能毁容的皮疹患者来说更成功。目的探讨麻疹、腮腺炎和风疹(MMR)免疫治疗多发性软疣的疗效和安全性。患者和方法本研究纳入200例多发性mcc患者,每2周一次注射MMR疫苗,在2-3个病灶内注射MMR疫苗,其中最大的软体动物最多注射0.3 ml,每2周间隔(第0、2、4、6、8周),最多注射5次,或直到mcc完全消退,以较早者为准。MMR疫苗的作用是通过减少病变数量和病变消退的时间来评估的。分析所有患者在后续就诊时(治疗开始后第2、4、6、8和10周,即第0周)的反应。所有患者在治疗开始前、治疗期间以及随访1个月(第14周)和3个月(第22周)时均进行了摄影记录。结果在200例患者中,184例完成了研究。其中男性116人,女性84人。研究参与者的平均年龄为17.17±12.64岁。研究结束时,149例(81%)患者MC完全消退,21例(11.4%)患者出现相对缓解,14例(7.6%)患者出现不良反应。25例(12.5%)患者在注射过程中出现轻度可耐受疼痛,17例(8.5%)患者出现色素改变,12例(6%)患者出现瘢痕形成。结论MMR疫苗局灶内免疫治疗是一种安全有效的治疗多发性硬化症的方法。
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Efficacy of intralesional measles, mumps and rubella vaccine immunotherapy in Molluscum contagiosum: a prospective study
Introduction Molluscum contagiosum(MC) is a viral infection of the skin and mucous membrane characterized by single or multiple, pearly white to flesh-colored umbilicated papules. There are certain therapies that increase the cellular immune response either through a topical or systemic approach as cell-mediated immunity plays an important role in the regression of MC. Immunomodulatory medications are relatively newer modalities of treatment that have been more successful for patients with widespread and potentially disfiguring eruptions. Objective To study the effect and safety of Measles, Mumps, and Rubella (MMR) immunotherapy in patients with multiple Mollusca. Patients and methods The study included 200 patients with multiple MC. They were injected with the MMR vaccine intralesionally into 2-3 lesions including the largest mollusca up to a maximum of 0.3 ml in one sitting every 2 weeks for a maximum of 5 treatments at a 2-week interval (week: 0, 2, 4, 6, 8) or till the complete resolution of MC whichever was earlier. The action of the MMR vaccine was assessed by the reduction of the number of lesions and the day of resolution of lesions. The response of all patients at subsequent visits (at second, fourth, sixth, eighth, and 10th week from the initiation of therapy which was taken as week 0) was analyzed. All the patients were subjected to photographic documentation before the initiation of therapy, during therapy, and at 1 month (week 14) and 3 months (week-22) of the follow-up period. Results Out of 200 patients, 184 completed the study. There were 116 males and 84 females. The mean age of study participants was 17.17±12.64 years. At the end of the study complete resolution of MC was seen in 149 (81%) patients, 21 (11.4%) patients had relative response while a poor response was seen in 14 (7.6%) of patients. Mild tolerable pain was seen in 25 (12.5%) patients during injection followed by pigmentary changes in 17 (8.5%) patients and scarring in 12 (6%) patients. Conclusion Intralesional immunotherapy with the MMR vaccine is an effective and safe modality for the treatment of MC.
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来源期刊
CiteScore
0.50
自引率
0.00%
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0
审稿时长
17 weeks
期刊介绍: The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.
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