免疫球蛋白g4相关炎性腹主动脉瘤伴多种罕见并发症的罕见临床病程。

Case Reports in Vascular Medicine Pub Date : 2019-06-03 eCollection Date: 2019-01-01 DOI:10.1155/2019/8249061
Yuji Naito, Tsukasa Miyatake, Manami Iwasaki, Atsushi Okuyama, Akio Takada, Koji Chiba, Masahiko Obata, Junichi Oba
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引用次数: 0

摘要

免疫球蛋白G4- (IgG4-)相关炎症性腹主动脉瘤(AAA)已被认为是IgG4相关疾病(IgG4- rd)的一种表现。我们有1例igg4相关炎症性AAA (IAAA)患者在血管内支架植入术前后出现多个连续表现。患者71岁,因血清IgG4浓度增高,腮腺活检表现典型,并伴有主动脉周炎,于就诊前2年零7个月在另一家医院确诊为IgG4- rd。他来我们医院是因为腹痛和腹痛。住院后出现截瘫,接受血管内支架植入术治疗IAAA。支架移植后约1个月,患者因肠炎出现乙状结肠穿孔。他还患有心肌梗塞。最后,他死于肠道出血。在这里,我们描述了这种罕见的、多重的、连续的IgG4-RD表现,其中一些可能是由igg4相关的IAAA或治疗副作用引起的,而不是由IgG4-RD本身引起的。我们报告这个病例是因为IgG4-RD或igg4相关IAAA的临床病程似乎很少见。用igg4相关IAAA治疗IgG4-RD时,应考虑引起症状的因素,慎重选择合适的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications.

Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications.

Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications.

Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications.

Immunoglobulin G4- (IgG4-) related inflammatory abdominal aortic aneurysm (AAA) has been recognized as a manifestation of IgG4-related disease (IgG4-RD). We experienced one patient with multiple consecutive manifestations before and after endovascular stent grafting for IgG4-related inflammatory AAA (IAAA). A 71-year-old man was diagnosed with IgG4-RD due to increased IgG4 serum concentration, typical findings of parotid gland biopsy, and periaortitis in another hospital 2 years and 7 months before visiting our hospital. He came to our hospital because of abdominal pain and IAAA. He developed paraplegia after hospitalization and underwent endovascular stent grafting for the IAAA. About one month after stent grafting, he developed perforation of the sigmoid colon due to enteritis. He also had myocardial infarction. Finally, he died of intestinal bleeding. Here, we describe this case with rare, multiple, consecutive manifestations of IgG4-RD, some of which might be caused by IgG4-related IAAA or side effects of treatments rather than by IgG4-RD itself. We report this case because the clinical course seemed rare for IgG4-RD or IgG4-related IAAA. For treating IgG4-RD with IgG4-related IAAA, we should consider factors causing the symptoms and carefully select the proper treatment.

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