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异时性双侧免疫球蛋白G4相关性胸膜炎:一例报告及文献复习

Metachronous bilateral immunoglobulin G4-related pleuritis: A case report and literature review.

作者信息

Tanabe Keitaro, Homma Takahiro, Matsui Shoko, Tsuchiya Tomoshi, Saji Hisashi

机构信息

Division of Thoracic Surgery University of Toyama Toyama Japan.

Division of Thoracic Surgery Kurobe City Hospital Kurobe Japan.

出版信息

Respirol Case Rep. 2023 Aug 16;11(9):e01204. doi: 10.1002/rcr2.1204. eCollection 2023 Sep.

DOI:10.1002/rcr2.1204
PMID:37593372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10427978/
Abstract

Immunoglobulin G4-related disease (IgG4-RD) is a newly recognized disease, and therefore its clinical features are not yet fully understood. Here, we describe a surgical case of metachronous bilateral IgG4-related pleuritis and postoperative chylothorax. This case could provide key insights into the pathology of IgG4-RD from a surgical perspective. We present a 70-year-old woman who had a right pleural mass. Video-assisted thoracoscopic pleural mass resection was performed, and the patient was diagnosed with right-sided IgG4-related pleuritis. Two years later, she was also diagnosed with left-sided IgG4-related pleuritis. We suspected the presence of IgG4-positive plasma cell infiltration. Additionally, she experienced a complicated postoperative chylothorax on the left side. It is important to consider the altered course of lymphatic vessels when extensively removing the pleura near the right thoracic duct. The occurrence of metachronous bilateral IgG4-associated pleuritis has not been previously reported, making this case particularly significant for understanding the pathology of IgG4-RD from a surgical standpoint.

摘要

免疫球蛋白G4相关性疾病(IgG4-RD)是一种新发现的疾病,因此其临床特征尚未完全明确。在此,我们描述一例异时性双侧IgG4相关性胸膜炎及术后乳糜胸的外科病例。该病例能够从外科角度为IgG4-RD的病理学提供关键见解。我们报告一名70岁女性,她有右侧胸膜肿块。进行了电视辅助胸腔镜下胸膜肿块切除术,患者被诊断为右侧IgG4相关性胸膜炎。两年后,她又被诊断为左侧IgG4相关性胸膜炎。我们怀疑存在IgG4阳性浆细胞浸润。此外,她术后左侧发生了乳糜胸并发症。在广泛切除右胸导管附近的胸膜时,考虑淋巴管走行的改变很重要。异时性双侧IgG4相关性胸膜炎的发生此前未见报道,因此该病例对于从外科角度理解IgG4-RD的病理学具有特殊意义。

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本文引用的文献

1
A case of immunoglobulin G4-Related disease with pleural effusion, requiring exclusion of tuberculous pleurisy.1例伴有胸腔积液的免疫球蛋白G4相关性疾病,需排除结核性胸膜炎。
Respir Med Case Rep. 2022 Apr 25;37:101654. doi: 10.1016/j.rmcr.2022.101654. eCollection 2022.
2
Pleural Involvement in IgG4-Related Disease: Case Report and Review of the Literature.IgG4相关性疾病中的胸膜受累:病例报告及文献综述
Diagnostics (Basel). 2021 Nov 23;11(12):2177. doi: 10.3390/diagnostics11122177.
3
Immunoglobulin G4-related Pleuritis Complicated with Minimal Change Disease.
免疫球蛋白 G4 相关性胸膜炎合并微小病变性肾病。
Intern Med. 2022 Mar 1;61(5):723-728. doi: 10.2169/internalmedicine.7010-20. Epub 2021 Sep 4.
4
Follicular lymphoma with hepatic accumulation on FDG-PET/CT masquerading IgG4-related disease.FDG-PET/CT显示肝脏有积聚的滤泡性淋巴瘤伪装成IgG4相关疾病。
Radiol Case Rep. 2021 Aug 1;16(10):2886-2889. doi: 10.1016/j.radcr.2021.07.008. eCollection 2021 Oct.
5
Pleuritis associated with immunoglobulin G4-related disease under normal thoracoscopic findings: a case report.正常胸腔镜检查结果下与免疫球蛋白G4相关疾病相关的胸膜炎:一例报告
J Med Case Rep. 2021 Apr 30;15(1):241. doi: 10.1186/s13256-021-02718-4.
6
IgG4-related pleural effusion with high adenosine deaminase levels: A case report and literature review.腺苷脱氨酶水平升高的IgG4相关性胸腔积液:一例报告及文献复习
Medicine (Baltimore). 2021 Mar 19;100(11):e25162. doi: 10.1097/MD.0000000000025162.
7
Refractory IgG4-related Pleural Disease with Chylothorax: A Case Report and Literature Review.难治性IgG4相关性胸腔积液伴乳糜胸:一例报告及文献复习
Intern Med. 2021 Jul 1;60(13):2135-2143. doi: 10.2169/internalmedicine.6313-20. Epub 2021 Feb 1.
8
IgG4-related disease with elevated adenosine deaminase in pleural effusion diagnosed clinically using thoracoscopy under local anesthesia and FDG-PET-CT.通过局部麻醉下胸腔镜检查及氟代脱氧葡萄糖正电子发射断层显像-计算机断层扫描(FDG-PET-CT)临床诊断的胸腔积液中腺苷脱氨酶升高的IgG4相关性疾病。
Respir Med Case Rep. 2020 Apr 25;30:101066. doi: 10.1016/j.rmcr.2020.101066. eCollection 2020.
9
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Respirol Case Rep. 2020 Mar 10;8(4):e00550. doi: 10.1002/rcr2.550. eCollection 2020 May.
10
Characteristics of pleural effusion in IgG4-related pleuritis.IgG4相关性胸膜炎中胸腔积液的特征
Respir Med Case Rep. 2020 Feb 6;29:101019. doi: 10.1016/j.rmcr.2020.101019. eCollection 2020.