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IgG4相关性疾病的肺血管受累:符合PRISMA标准的系统评价病例系列

Pulmonary vascular involvement of IgG4-related disease: Case series with a PRISMA-compliant systemic review.

作者信息

Zhou Yong, Shao Lingyan, Ruan Wenjing, Jin Joy, Xu Hangdi, Ying Kejing, Wu Xiaohong

机构信息

Respiratory and Critical Care Medicine, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

Thoracic Oncology Program, Department of Surgery, Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, CA.

出版信息

Medicine (Baltimore). 2019 Feb;98(6):e14437. doi: 10.1097/MD.0000000000014437.

DOI:10.1097/MD.0000000000014437
PMID:30732204
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6380675/
Abstract

BACKGROUND

Immunoglobulin G4-related disease (IgG4-RD) is a recently recognized, immune-mediated chronic fibrotic inflammation that can involve almost all organs, causing tumefaction and dysfunction. Its presence in pulmonary circulation is underestimated and has not yet been investigated.

OBJECTIVES

We describe a representative IgG4-RD patient with pulmonary artery stenosis and pulmonary embolism, leading to reversible pulmonary hypertension. Literature review of IgG4-RD with pulmonary circulation involvement was conducted.

DATA SOURCES

References for this review were identified through searches via PubMed, EBSCO, and Web of Science for published articles before November 2016.

RESULTS

There were 15 published cases of IgG4-RD with pulmonary vascular involvement, 3 with pulmonary arteritis, 2 with pulmonary artery aneurysm, 3 with pulmonary artery stenosis, 1 with obliterative phlebitis, and 1 with pulmonary embolism. Possible immunity and inflammation mechanisms were summarized.

CONCLUSIONS

IgG4-RD with pulmonary vascular involvement is rare. Echocardiogram and contrast-enhanced chest CT are helpful to screen the disease. Clinical manifestations were found from asymptomatic to dyspnea or even syncope. And nearly all cases had more than 1 organ affected, with significantly increased serum IgG4 levels. PET/CT aided in identifying affected organs and determining candidate biopsy sites. More awareness is urged to evaluate the pulmonary vascular manifestations of this disease.

摘要

背景

免疫球蛋白G4相关性疾病(IgG4-RD)是一种最近才被认识的、免疫介导的慢性纤维化炎症,可累及几乎所有器官,导致肿胀和功能障碍。其在肺循环中的存在被低估,尚未得到研究。

目的

我们描述了一名具有代表性的IgG4-RD患者,其患有肺动脉狭窄和肺栓塞,导致可逆性肺动脉高压。对IgG4-RD累及肺循环的文献进行了综述。

数据来源

通过在PubMed、EBSCO和Web of Science上检索2016年11月之前发表的文章来确定本综述的参考文献。

结果

已发表15例IgG4-RD累及肺血管的病例,其中3例有肺动脉炎,2例有肺动脉瘤,3例有肺动脉狭窄,1例有闭塞性静脉炎,1例有肺栓塞。总结了可能的免疫和炎症机制。

结论

IgG4-RD累及肺血管较为罕见。超声心动图和胸部增强CT有助于筛查该病。临床表现从无症状到呼吸困难甚至晕厥。几乎所有病例都有不止一个器官受累,血清IgG4水平显著升高。PET/CT有助于识别受累器官并确定候选活检部位。迫切需要提高对该病肺血管表现的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/b25b2a77bb13/medi-98-e14437-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/196cb3541f3c/medi-98-e14437-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/65a77219fcc7/medi-98-e14437-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/3a9853b7dc55/medi-98-e14437-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/723b6feb5c03/medi-98-e14437-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/b25b2a77bb13/medi-98-e14437-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/196cb3541f3c/medi-98-e14437-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/65a77219fcc7/medi-98-e14437-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/3a9853b7dc55/medi-98-e14437-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/723b6feb5c03/medi-98-e14437-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/6380675/b25b2a77bb13/medi-98-e14437-g005.jpg

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Long-term clinical course and outcomes of immunoglobulin G4-related lung disease.免疫球蛋白 G4 相关肺部疾病的长期临床病程和结局。
Respir Res. 2020 Oct 19;21(1):273. doi: 10.1186/s12931-020-01542-6.
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The filling defect of pulmonary artery, an imaging finding what we should know.肺动脉充盈缺损,一项我们应该了解的影像学表现。
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