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脑出血合并变应性肉芽肿性血管炎:多学科协作与文献综述

Intracerebral Hemorrhage with Churg Strauss-Syndrome: Multidisciplinary Collaboration and Literature Review.

作者信息

Bai Pu, Xie Peitao

机构信息

Inner Mongolia Medical University Ordos School of Clinical Medicine, Ordos, 017000, People's Republic of China.

出版信息

Vasc Health Risk Manag. 2024 Dec 14;20:567-578. doi: 10.2147/VHRM.S489212. eCollection 2024.

DOI:10.2147/VHRM.S489212
PMID:39698545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11653849/
Abstract

OBJECTIVE

To explore the clinical characteristics and treatment outcomes of intracerebral hemorrhage in eosinophilic granulomatosis with polyangiitis (EGPA).

METHODS AND PATIENT PRESENTATION

We report an 18-year-old student of EGPA complicated with intracerebral hemorrhage. The laboratory tests showed a continuous increase in eosinophils. The CT of head and chest showed cerebral hemorrhage and pulmonary infiltration.

INTERVENTIONS

The patient received an intravenous infusion of methylprednisolone 1g/(kg·d) and cyclophosphamide for 3 days, followed by oral prednisone 1 mg/(kg·d).

OUTCOMES

At discharge, the patient's head and chest CT showed obvious absorption of intracranial hematoma and improvement of pulmonary infiltration. We reviewed 40 previously published cases of EGPA with intracerebral hemorrhage focusing on the clinical features and treatment of intracerebral hemorrhage caused by EGPA.

CONCLUSION

For the cases of EGPA complicated with intracerebral hemorrhage, we should timely differentiate diagnosis and recognition. Early diagnosis with aggressive immunosuppressive therapy can help improve the prognosis of patients EGPA with intracerebral hemorrhage. When a patient is affected by EGPA, it is essential to remain vigilant for signs of Central Nervous System involvement. The treatment with glucocorticoids and cyclophosphamide is effective in managing EGPA.

摘要

目的

探讨嗜酸性肉芽肿性多血管炎(EGPA)合并脑出血的临床特征及治疗效果。

方法及病例介绍

我们报告一名18岁的EGPA学生,并发脑出血。实验室检查显示嗜酸性粒细胞持续升高。头颅和胸部CT显示脑出血和肺部浸润。

干预措施

患者接受静脉输注甲泼尼龙1g/(kg·d)和环磷酰胺3天,随后口服泼尼松1mg/(kg·d)。

结果

出院时,患者的头颅和胸部CT显示颅内血肿明显吸收,肺部浸润改善。我们回顾了40例先前发表的EGPA合并脑出血的病例,重点关注EGPA所致脑出血的临床特征和治疗。

结论

对于EGPA合并脑出血的病例,应及时进行鉴别诊断和识别。早期诊断并积极进行免疫抑制治疗有助于改善EGPA合并脑出血患者的预后。当患者患有EGPA时,必须对中枢神经系统受累的迹象保持警惕。糖皮质激素和环磷酰胺治疗对管理EGPA有效。

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本文引用的文献

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Kaohsiung J Med Sci. 2024 Oct;40(10):949-950. doi: 10.1002/kjm2.12882. Epub 2024 Aug 19.
2
Eosinophilic granulomatous polyangiitis with central nervous system involvement in children: a case report and literature review.儿童嗜酸性肉芽肿性多血管炎伴中枢神经系统受累:病例报告及文献复习。
Front Immunol. 2024 May 15;15:1406424. doi: 10.3389/fimmu.2024.1406424. eCollection 2024.
3
A case of subarachnoid haemorrhage associated with MPO-ANCA-positive eosinophilic granulomatosis with polyangiitis, successfully treated with glucocorticoid, cyclophosphamide, and mepolizumab.
一例伴 MPO-ANCA 阳性嗜酸性肉芽肿性多血管炎的蛛网膜下腔出血,经糖皮质激素、环磷酰胺和美泊利珠单抗治疗后成功。
Mod Rheumatol Case Rep. 2024 Jul 8;8(2):310-313. doi: 10.1093/mrcr/rxad071.
4
Acute paraplegia in a patient with eosinophilic granulomatosis and polyangiitis with 20 years of evolution: case report.患者患有嗜酸性肉芽肿性多血管炎,病程长达 20 年,出现急性截瘫:病例报告。
Acta Biomed. 2023 Dec 5;94(6):e2023243. doi: 10.23750/abm.v95i1.14209.
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Eosinophilic Granulomatosis with Polyangiitis (EGPA): A case report with atypical presentation.嗜酸性肉芽肿性多血管炎(EGPA):一例非典型表现的病例报告。
Pak J Med Sci. 2023 Jan-Feb;39(1):307-309. doi: 10.12669/pjms.39.1.6436.
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2022 American College of Rheumatology/European Alliance of Associations for Rheumatology Classification Criteria for Granulomatosis With Polyangiitis.2022 年美国风湿病学会/欧洲风湿病联盟肉芽肿性多血管炎分类标准。
Arthritis Rheumatol. 2022 Mar;74(3):393-399. doi: 10.1002/art.41986. Epub 2022 Feb 2.
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