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本文引用的文献

1
Successful treatment of rituximab in a steroid-dependent immunoglobulin A vasculitis patient with gastrointestinal involvement: a case report.利妥昔单抗成功治疗一例合并胃肠道受累的类固醇依赖型免疫球蛋白A血管炎患者:病例报告
Scand J Rheumatol. 2023 May;52(3):324-325. doi: 10.1080/03009742.2022.2154525. Epub 2023 Jan 12.
2
Pathogenesis of IgA Vasculitis: An Up-To-Date Review.IgA 血管炎的发病机制:最新综述。
Front Immunol. 2021 Nov 9;12:771619. doi: 10.3389/fimmu.2021.771619. eCollection 2021.
3
IgA Vasculitis in Adults: a Rare yet Challenging Disease.成人 IgA 血管炎:一种罕见但极具挑战性的疾病。
Curr Rheumatol Rep. 2021 Jul 1;23(7):50. doi: 10.1007/s11926-021-01013-x.
4
Henoch-Schönlein Purpura (IgA Vasculitis): Rapid Evidence Review.过敏性紫癜(IgA 血管炎):快速证据回顾。
Am Fam Physician. 2020 Aug 15;102(4):229-233.
5
Rituximab treatment for chronic steroid-dependent Henoch-Schonlein purpura: 8 cases and a review of the literature.利妥昔单抗治疗慢性类固醇依赖型过敏性紫癜:8例报告及文献复习
Pediatr Rheumatol Online J. 2018 Nov 14;16(1):71. doi: 10.1186/s12969-018-0285-2.
6
Brief Report: Rituximab for the Treatment of Adult-Onset IgA Vasculitis (Henoch-Schönlein).简要报告:利妥昔单抗治疗成人 IgA 血管炎(过敏性紫癜)。
Arthritis Rheumatol. 2018 Jan;70(1):109-114. doi: 10.1002/art.40339. Epub 2017 Dec 1.
7
Henoch-Schönlein Purpura: A Literature Review.过敏性紫癜:文献综述。
Acta Derm Venereol. 2017 Nov 15;97(10):1160-1166. doi: 10.2340/00015555-2733.
8
An adult case of severe steroid-resistant Henoch-Schönlein purpura nephritis treated with intravenous cyclophosphamide and tonsillectomy.1例成年重症激素抵抗型过敏性紫癜性肾炎患者接受静脉注射环磷酰胺及扁桃体切除术治疗。
CEN Case Rep. 2016 Nov;5(2):212-218. doi: 10.1007/s13730-016-0227-0. Epub 2016 Jul 13.
9
Azathioprine therapy for steroid-resistant Henoch-Schönlein purpura: a report of 6 cases.硫唑嘌呤治疗激素抵抗型过敏性紫癜:6例报告
Pediatr Rheumatol Online J. 2016 Jun 23;14(1):37. doi: 10.1186/s12969-016-0100-x.
10
Mycophenolate mofetil plus prednisone for inducing remission of Henoch-Schönlein purpura nephritis: a retrospective study.霉酚酸酯联合泼尼松诱导紫癜性肾炎缓解:一项回顾性研究
J Zhejiang Univ Sci B. 2015 Sep;16(9):772-9. doi: 10.1631/jzus.B1400335.

一名19岁女性的类固醇依赖型复发性IgA血管炎

Steroid-Dependent Recurrent IgA Vasculitis in a 19-Year-Old Woman.

作者信息

Berrett Hannah, Gohil Shivangi, Kurian Rebecca, Neyman Patricia

机构信息

Menorah Medical Center, Overland Park, KS.

出版信息

HCA Healthc J Med. 2024 Aug 1;5(4):453-458. doi: 10.36518/2689-0216.1660. eCollection 2024.

DOI:10.36518/2689-0216.1660
PMID:39290479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11404596/
Abstract

BACKGROUND

Immunoglobulin A (IgA) vasculitis is common in children and typically resolves spontaneously. However, when presenting in adults, it is more likely to be severe and recurrent.

CASE PRESENTATION

We present the case of a 19-year-old female patient with recurrent steroid-dependent IgA vasculitis. She had a history of a prolonged episode of IgA vasculitis in childhood. She presented to our hospital with proteinuria and a painful, palpable purpuric rash on her bilateral lower extremities. She was treated with high-dose intravenous steroids. When steroids were tapered, the patient had a recurrence of her painful rash. Over several months, she developed steroid-induced hyperglycemia and worsening proteinuria.

CONCLUSION

Recent studies have shown that corticosteroids have limited effect on long-term outcomes in IgA vasculitis, but steroid-sparing agents have potential for the treatment of recurrent steroid-dependent IgA vasculitis.

摘要

背景

免疫球蛋白A(IgA)血管炎在儿童中很常见,通常会自发缓解。然而,在成人中发病时,病情更可能较为严重且易复发。

病例报告

我们报告一例19岁复发性依赖类固醇的IgA血管炎女性患者。她童年时有过一次持续时间较长的IgA血管炎发作史。她因蛋白尿以及双侧下肢疼痛性可触及的紫癜性皮疹前来我院就诊。她接受了大剂量静脉注射类固醇治疗。当类固醇减量时,患者疼痛性皮疹复发。在几个月的时间里,她出现了类固醇诱导的高血糖症且蛋白尿加重。

结论

最近的研究表明,皮质类固醇对IgA血管炎的长期预后影响有限,但类固醇节约剂有治疗复发性依赖类固醇的IgA血管炎的潜力。