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人疱疹病毒感染并发 acquired epidermolysis bullosa。

Human orf complicated by epidermolysis bullosa acquisita.

机构信息

Dermatology Department, Saint-Louis Hospital, 1 Avenue Claude Vellefaux, 75010, Paris, France.

Paris VII Sorbonne Paris Cité University, Paris, France.

出版信息

Br J Dermatol. 2018 Feb;178(2):547-550. doi: 10.1111/bjd.15496. Epub 2017 Oct 17.

DOI:10.1111/bjd.15496
PMID:28338219
Abstract

Orf is a DNA parapoxvirus transmitted to humans by contact with infected goats and sheep. Many complications have been reported after orf infection, including erythema multiforme. A few cases of autoimmune bullous dermatosis complicating orf disease have been reported to date. They are usually characterized by tense blister eruptions with or without mucosal involvement; linear deposition of C3, IgG and/or IgA along the basement membrane; and negativity of indirect immunofluorescence analysis and enzyme-linked immunosorbent assay (ELISA) (performed in four of 11 reported cases). These analyses have targeted antigens of bullous pemphigoid, mucous membrane pemphigoid or epidermolysis bullosa acquisita, except one case of mucosal pemphigoid with antilaminin-332 antibodies. We describe the case of a patient who presented with an ulceration on his finger 10 days after direct contact with a lamb during Eid al-Adha. Four weeks later he developed a severe tense blistering eruption associated with mucous membrane erosions. Indirect immunofluorescence analysis using the patient's serum revealed circulating antibasement membrane IgG that bound the dermal side of salt-split skin. ELISA was positive for recombinant immunodominant NC1 domain of type VII collagen. We finally diagnosed epidermolysis bullosa acquisita complicating probable human orf infection.

摘要

羊痘是一种由感染的山羊和绵羊通过接触传播给人类的 DNA 副痘病毒。感染羊痘后会出现许多并发症,包括多形红斑。迄今为止,已有少数自身免疫性大疱性皮肤病并发羊痘的病例报告。它们通常表现为紧张性水疱性皮疹,伴或不伴有黏膜受累;沿基底膜线状沉积 C3、IgG 和/或 IgA;间接免疫荧光分析和酶联免疫吸附试验(ELISA)均为阴性(在 11 例报告病例中的 4 例中进行)。这些分析的靶抗原为大疱性类天疱疮、黏膜性类天疱疮或获得性大疱性表皮松解症,除了一例抗层粘连蛋白 332 抗体的黏膜性类天疱疮。我们描述了一例患者的病例,他在宰牲节期间直接接触羔羊 10 天后手指出现溃疡,4 周后他出现严重的紧张性水疱性皮疹,并伴有黏膜糜烂。使用患者血清进行间接免疫荧光分析显示循环抗基底膜 IgG 结合盐裂皮肤的真皮侧。ELISA 对重组免疫显性 VII 型胶原 NC1 结构域呈阳性。我们最终诊断为获得性大疱性表皮松解症并发可能的人类羊痘感染。

相似文献

1
Human orf complicated by epidermolysis bullosa acquisita.人疱疹病毒感染并发 acquired epidermolysis bullosa。
Br J Dermatol. 2018 Feb;178(2):547-550. doi: 10.1111/bjd.15496. Epub 2017 Oct 17.
2
Orf-induced immunobullous disease: A distinct autoimmune blistering disorder.羊痘疮引起的免疫性大疱性疾病:一种独特的自身免疫性大疱性疾病。
J Am Acad Dermatol. 2008 Jan;58(1):49-55. doi: 10.1016/j.jaad.2007.08.029. Epub 2007 Oct 4.
3
A case of mixed bullous disease of epidermolysis bullosa acquisita and linear IgA bullous dermatosis.1例获得性大疱性表皮松解症与线状IgA大疱性皮肤病混合型病例。
Dermatology. 2005;211(2):146-8. doi: 10.1159/000086445.
4
Childhood Epidermolysis Bullosa Acquisita: Confirmation of Diagnosis by Skin Deficient in Type VII Collagen, Enzyme-linked Immunosorbent Assay, and Immunoblotting.儿童获得性大疱性表皮松解症:通过VII型胶原蛋白缺乏的皮肤、酶联免疫吸附测定和免疫印迹法确诊
Indian J Dermatol. 2016 May-Jun;61(3):329-32. doi: 10.4103/0019-5154.182420.
5
A case of an inflammatory variant of epidermolysis bullosa acquisita: chronic bullous dermatosis associated with nonscarring mucosal blisters and circulating IgG anti-type-VII-collagen antibody.获得性大疱性表皮松解症的一种炎症变体病例:与无瘢痕性黏膜水疱和循环IgG抗VII型胶原蛋白抗体相关的慢性大疱性皮肤病。
Dermatology. 1998;197(1):58-61. doi: 10.1159/000017958.
6
Passive transfer of autoantibodies from a patient with mutilating epidermolysis bullosa acquisita induces specific alterations in the skin of neonatal mice.来自一名获得性致残性大疱性表皮松解症患者的自身抗体被动转移可诱导新生小鼠皮肤发生特异性改变。
Arch Dermatol. 1995 May;131(5):590-5.
7
Epidermolysis bullosa acquisita and anti-p200 pemphigoid as major subepidermal autoimmune bullous diseases diagnosed by floor binding on indirect immunofluorescence microscopy using human salt-split skin.获得性大疱性表皮松解症和抗p200类天疱疮是主要的表皮下自身免疫性大疱病,通过使用人盐裂皮肤的间接免疫荧光显微镜检查中的基底膜带结合来诊断。
Indian J Dermatol Venereol Leprol. 2017 Sep-Oct;83(5):550-555. doi: 10.4103/ijdvl.IJDVL_678_16.
8
IgA-epidermolysis bullosa acquisita in a child resulting in blindness.
Br J Dermatol. 1997 Aug;137(2):270-5. doi: 10.1046/j.1365-2133.1997.18191915.x.
9
Case of epidermolysis bullosa acquisita with concomitant anti-laminin-332 antibodies.获得性大疱性表皮松解症伴抗层粘连蛋白 332 抗体。
J Dermatol. 2018 Apr;45(4):472-474. doi: 10.1111/1346-8138.14169. Epub 2017 Dec 4.
10
Distinguishing Epidermolysis Bullosa Acquisita From Bullous Pemphigoid Without Direct Immunofluorescence.在无直接免疫荧光情况下鉴别获得性大疱性表皮松解症与大疱性类天疱疮
J Cutan Med Surg. 2018 Jan/Feb;22(1):22-24. doi: 10.1177/1203475417722734. Epub 2017 Jul 18.

引用本文的文献

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Finger nodules with a papulovesicular hands and feet eruption: a complicated human Orf virus infection.手指结节伴手足部丘疹水疱样发疹:复杂的人传染性软疣病毒感染。
BMC Infect Dis. 2024 Jan 17;24(1):95. doi: 10.1186/s12879-024-08998-7.
2
Autoimmunity against laminin 332.抗层粘连蛋白 332 的自身免疫
Front Immunol. 2023 Aug 10;14:1250115. doi: 10.3389/fimmu.2023.1250115. eCollection 2023.
3
Human Orf with Immune-Mediated Reactions: A Systematic Review.伴有免疫介导反应的人传染性软疣:一项系统评价
Microorganisms. 2023 Apr 27;11(5):1138. doi: 10.3390/microorganisms11051138.
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A Review on Human Orf: A Neglected Viral Zoonosis.关于人类传染性脓疱病的综述:一种被忽视的病毒性人畜共患病。
Res Rep Trop Med. 2021 Jul 8;12:153-172. doi: 10.2147/RRTM.S306446. eCollection 2021.