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导致声门下狭窄的免疫球蛋白G4相关性疾病(IgG4-RD)的一种不寻常表现。

An Unusual Presentation of Immunoglobulin G4-Related Disease (IgG4-RD) Causing Subglottic Stenosis.

作者信息

Nallani Prakash, Guo Weixia, Mayerhoff Ross M, Meysami Alireza

机构信息

Rheumatology, Henry Ford Health System, Detroit, USA.

Rheumatology, Wayne State University Detroit Medical Center, Detroit, USA.

出版信息

Cureus. 2022 Jun 23;14(6):e26250. doi: 10.7759/cureus.26250. eCollection 2022 Jun.

Abstract

Immunoglobulin G4-related disease (IgG4-RD) is an immune-mediated fibroinflammatory condition that is known to involve multiple organs and was first described as an entity in 2003. It is characterized by lesions with a dense lymphoplasmacytic infiltrate, IgG4-positive plasma cells, storiform fibrosis, and frequently elevated serum IgG4 levels. Organs that are commonly involved include the pancreas, biliary tree, salivary glands, periorbital tissues, kidneys, retroperitoneum, lungs, pleura, thyroid, aorta, and lymph nodes. Rarer manifestations of IgG4-RD include central nervous system (CNS) involvement, prostatitis, mastitis, midline destructive disease, and nasopharyngeal disease. In this report, we discuss an atypical case of a young woman with laryngeal subglottic involvement leading to stenosis and airway obstruction, which was ultimately successfully managed with systemic immunosuppression.

摘要

免疫球蛋白G4相关疾病(IgG4-RD)是一种免疫介导的纤维炎症性疾病,已知可累及多个器官,于2003年首次被描述为一种独立的疾病实体。其特征为病变处有密集的淋巴浆细胞浸润、IgG4阳性浆细胞、席纹状纤维化,且血清IgG4水平常升高。常见受累器官包括胰腺、胆道、唾液腺、眶周组织、肾脏、腹膜后、肺、胸膜、甲状腺、主动脉和淋巴结。IgG4-RD较罕见的表现包括中枢神经系统(CNS)受累、前列腺炎、乳腺炎、中线破坏性疾病和鼻咽部疾病。在本报告中,我们讨论了一例年轻女性的非典型病例,其喉下咽部受累导致狭窄和气道阻塞,最终通过全身免疫抑制成功治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9464/9313090/88b64c3f1b36/cureus-0014-00000026250-i01.jpg

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