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Detection of Borrelia burgdorferi DNA (B garinii or B afzelii) in morphea and lichen sclerosus et atrophicus tissues of German and Japanese but not of US patients.在德国和日本患者的硬斑病及硬化萎缩性苔藓组织中检测到伯氏疏螺旋体DNA(伽氏疏螺旋体或阿氏疏螺旋体),而在美国患者中未检测到。
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引用本文的文献

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Morphea in two patients after being infected to and being vaccinated against SARS-CoV-2 infection.两名感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)并接种疫苗后出现硬斑病的患者。
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Biosimilars in dermatology: The wind of change.皮肤科生物类似药:变革之风。
Exp Ther Med. 2019 Aug;18(2):911-915. doi: 10.3892/etm.2019.7505. Epub 2019 Apr 18.
2
Therapeutic management with biological anti-TNF-α agent in severe psoriasis associated with chronic hepatitis B: A case report.生物抗TNF-α制剂治疗慢性乙型肝炎相关的重度银屑病:一例报告
Exp Ther Med. 2019 Aug;18(2):895-899. doi: 10.3892/etm.2019.7567. Epub 2019 May 9.
3
Disease recurrence in localized scleroderma: a retrospective analysis of 344 patients with paediatric- or adult-onset disease.局限性硬皮病的疾病复发:344 例儿童或成人发病患者的回顾性分析。
Br J Dermatol. 2015 Mar;172(3):722-8. doi: 10.1111/bjd.13514. Epub 2015 Feb 8.
4
Treatment of morphea or localized scleroderma: review of the literature.硬斑病或局限性硬皮病的治疗:文献综述
J Drugs Dermatol. 2010 Oct;9(10):1213-9.
5
Treatment of recalcitrant generalized morphea with infliximab.用英夫利昔单抗治疗顽固性泛发性硬斑病。
Arch Dermatol. 2010 Jun;146(6):601-4. doi: 10.1001/archdermatol.2010.120.
6
Localized scleroderma.局限性硬皮病
Curr Opin Rheumatol. 2006 Nov;18(6):606-13. doi: 10.1097/01.bor.0000245727.40630.c3.
7
Pulsed high-dose corticosteroids combined with low-dose methotrexate in severe localized scleroderma.脉冲高剂量皮质类固醇联合低剂量甲氨蝶呤治疗重度局限性硬皮病
Arch Dermatol. 2005 Jul;141(7):847-52. doi: 10.1001/archderm.141.7.847.
8
Is morphoea caused by Borrelia burgdorferi? A review.莱姆病螺旋体是否会引发硬斑病?一篇综述。
Br J Dermatol. 2000 Apr;142(4):636-44. doi: 10.1046/j.1365-2133.2000.03407.x.
9
Topical calcipotriene for morphea/linear scleroderma.外用卡泊三醇治疗硬斑病/线状硬皮病。
J Am Acad Dermatol. 1998 Aug;39(2 Pt 1):211-5. doi: 10.1016/s0190-9622(98)70077-5.
10
Further evidence for Borrelia burgdorferi infection in morphea and lichen sclerosus et atrophicus confirmed by DNA amplification.通过DNA扩增证实硬斑病和萎缩性硬化性苔藓中存在伯氏疏螺旋体感染的进一步证据。
J Invest Dermatol. 1993 May;100(5):717-20. doi: 10.1111/1523-1747.ep12472369.

在硬斑病中的病因学作用:一例报告。

Etiologic role of in morphea: A case report.

作者信息

Șandru Florica, Popa Adelina, Petca Aida, Miulescu Raluca-Gabriela, Constantin Maria Magdalena, Petca Răzvan-Cosmin, Constantin Traian, Dumitrașcu Mihai Cristian

机构信息

'Carol Davila' University of Medicine and Pharmacy, 050474 Bucharest, Romania.

Department of Dermatology, 'Elias' Emergency University Hospital, 011461 Bucharest, Romania.

出版信息

Exp Ther Med. 2020 Sep;20(3):2373-2376. doi: 10.3892/etm.2020.8815. Epub 2020 May 29.

DOI:10.3892/etm.2020.8815
PMID:32765717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7401849/
Abstract

Morphea is an inflammatory skin disease with self-limited evolution, presenting as localized sclerosis of the skin and/or underlying tissues. The incidence is not exactly known; the disease occurs more frequently in women, and there is no sex prevalence. Pathogenesis of morphea remains still controversial. Several theories exist and the infection is not yet elucidated. The aim of this report is to present the main mechanisms involved in the etiophatogenesis of morphea and also the thepapeutic options. A case of a 60-year-old woman is presented, who was referred to the clinic for an erythematous-violaceus, asymptomatic eruption, located on the trunk and legs, for appoximately 2 months. The patient's medical history revealed an infection with 1 year previously. After diagnosis of morphea was established, and with systemic therapy (corticosteroids and methotrexate), the evolution was favorable.

摘要

硬斑病是一种具有自限性病程的炎症性皮肤病,表现为皮肤和/或皮下组织的局限性硬化。其发病率尚不完全清楚;该疾病在女性中更为常见,且无性别差异。硬斑病的发病机制仍存在争议。有多种理论,感染因素尚未阐明。本报告的目的是介绍硬斑病发病机制中的主要机制以及治疗选择。报告了一例60岁女性病例,该患者因躯干和腿部出现约2个月的紫红色、无症状皮疹而转诊至诊所。患者病史显示1年前曾有感染。硬斑病诊断确立后,经全身治疗(皮质类固醇和甲氨蝶呤),病情好转。