Paula Andrea Chacón-Jaramillo, Johana Andrea Gil-Ovalle, David Castillo-Molina, Rubén Darío Mantilla
{"title":"罗威尔综合征:病例报告及文献复习","authors":"Paula Andrea Chacón-Jaramillo, Johana Andrea Gil-Ovalle, David Castillo-Molina, Rubén Darío Mantilla","doi":"10.1016/j.rcreue.2023.10.001","DOIUrl":null,"url":null,"abstract":"<div><p><span>Rowell syndrome is a rare disease which consists of lesions of lupus erythematosus and erythema multiforme<span><span> in patients<span> with a characteristic immunological pattern, given by the presence of positive antinuclear antibodies<span> in a mottled pattern and the absence of infectious and/or pharmacologic triggers. We present a case of a 23-year-old woman with a 4-year history of recurrent episodes of vesicles and blisters, of soft consistency and erythematous base on upper and lower limbs, affecting the oral and nasal mucosa; associated with chilblains, </span></span></span>Raynaud's phenomenon, </span></span>ulcers<span><span> in oral and nasal mucosa and polyarthralgia<span>; skin biopsy reported erythema multiforme, with negative direct </span></span>immunofluorescence and positive speckled pattern antinuclear antibodies, findings that fulfil the diagnostic criteria of Zeitouni et al. (2000) and Torchia et al. (2012) for the diagnosis of Rowell's syndrome.</span></p></div>","PeriodicalId":101099,"journal":{"name":"Revista Colombiana de Reumatología (English Edition)","volume":"30 4","pages":"Pages 332-336"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rowell syndrome: Case report and review of the literature\",\"authors\":\"Paula Andrea Chacón-Jaramillo, Johana Andrea Gil-Ovalle, David Castillo-Molina, Rubén Darío Mantilla\",\"doi\":\"10.1016/j.rcreue.2023.10.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Rowell syndrome is a rare disease which consists of lesions of lupus erythematosus and erythema multiforme<span><span> in patients<span> with a characteristic immunological pattern, given by the presence of positive antinuclear antibodies<span> in a mottled pattern and the absence of infectious and/or pharmacologic triggers. We present a case of a 23-year-old woman with a 4-year history of recurrent episodes of vesicles and blisters, of soft consistency and erythematous base on upper and lower limbs, affecting the oral and nasal mucosa; associated with chilblains, </span></span></span>Raynaud's phenomenon, </span></span>ulcers<span><span> in oral and nasal mucosa and polyarthralgia<span>; skin biopsy reported erythema multiforme, with negative direct </span></span>immunofluorescence and positive speckled pattern antinuclear antibodies, findings that fulfil the diagnostic criteria of Zeitouni et al. (2000) and Torchia et al. (2012) for the diagnosis of Rowell's syndrome.</span></p></div>\",\"PeriodicalId\":101099,\"journal\":{\"name\":\"Revista Colombiana de Reumatología (English Edition)\",\"volume\":\"30 4\",\"pages\":\"Pages 332-336\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista Colombiana de Reumatología (English Edition)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2444440523000699\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Colombiana de Reumatología (English Edition)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2444440523000699","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
罗威尔综合征是一种罕见的疾病,由红斑狼疮和多形性红斑病变组成,患者具有典型的免疫模式,由于存在斑驳模式的阳性抗核抗体和缺乏感染和/或药物触发。我们报告一个23岁的女性病例,她有4年的反复发作的囊泡和水疱,软稠度和红斑基础在上肢和下肢,影响口腔和鼻黏膜;与冻疮、雷诺氏现象、口腔和鼻腔粘膜溃疡和多关节痛有关;皮肤活检报告多形红斑,直接免疫荧光阴性,斑点型抗核抗体阳性,符合Zeitouni等人(2000)和Torchia等人(2012)诊断罗威尔综合征的诊断标准。研究结果表明:①①①①①①①①①①①①①①①①①①①①①①①①①②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②②。目前,我们报告了23例小儿麻痹症años, 1例años, 2例evolución,复发性发作1例vesículas, 1例扁桃体炎,2例上、下、afectación, 1例口腔粘膜和鼻,2例伴有先天性先天性先天性脓疮(冻疮),1例fenómeno, 1例雷诺,1例口腔粘膜和鼻神经痛。报告性多形活组织病,免疫荧光直接阴性,反反核反应patrón阳性反应,hallazgos que cumplían反反标准diagnósticos Zeitouni等人año 2000; de Torchia等人2012 para el diagnóstico de síndrome de Rowell。
Rowell syndrome: Case report and review of the literature
Rowell syndrome is a rare disease which consists of lesions of lupus erythematosus and erythema multiforme in patients with a characteristic immunological pattern, given by the presence of positive antinuclear antibodies in a mottled pattern and the absence of infectious and/or pharmacologic triggers. We present a case of a 23-year-old woman with a 4-year history of recurrent episodes of vesicles and blisters, of soft consistency and erythematous base on upper and lower limbs, affecting the oral and nasal mucosa; associated with chilblains, Raynaud's phenomenon, ulcers in oral and nasal mucosa and polyarthralgia; skin biopsy reported erythema multiforme, with negative direct immunofluorescence and positive speckled pattern antinuclear antibodies, findings that fulfil the diagnostic criteria of Zeitouni et al. (2000) and Torchia et al. (2012) for the diagnosis of Rowell's syndrome.