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...

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Main Authors: Yuji Naito, Tsukasa Miyatake, Manami Iwasaki, Atsushi Okuyama, Akio Takada, Koji Chiba, Masahiko Obata, Junichi Oba
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Case Reports in Vascular Medicine
Online Access:http://dx.doi.org/10.1155/2019/8249061
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author Yuji Naito
Tsukasa Miyatake
Manami Iwasaki
Atsushi Okuyama
Akio Takada
Koji Chiba
Masahiko Obata
Junichi Oba
author_facet Yuji Naito
Tsukasa Miyatake
Manami Iwasaki
Atsushi Okuyama
Akio Takada
Koji Chiba
Masahiko Obata
Junichi Oba
author_sort Yuji Naito
collection DOAJ
description 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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spelling doaj-art-85c1d0edb94a4b8f8846e902cf0d45c62025-02-03T06:00:58ZengWileyCase Reports in Vascular Medicine2090-69862090-69942019-01-01201910.1155/2019/82490618249061Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare ComplicationsYuji Naito0Tsukasa Miyatake1Manami Iwasaki2Atsushi Okuyama3Akio Takada4Koji Chiba5Masahiko Obata6Junichi Oba7Department of Thoracic Surgery, Asahikawa City Hospital, Asahikawa, JapanDepartment of Cardiovascular Surgery, Hokko Memorial Hospital, Sapporo, JapanDepartment of Radiation Medicine, Hokkaido University Graduate School of Medicine, Sapporo, JapanDepartment of Internal Medicine, Fukagawa Municipal Hospital, Fukagawa, JapanDepartment of Pathology, Asahikawa City Hospital, Asahikawa, JapanDepartment of Hematology, Asahikawa City Hospital, Asahikawa, JapanDepartment of Pathology, Asahikawa Red Cross Hospital, Asahikawa, JapanDepartment of Cardiovascular Surgery, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, JapanImmunoglobulin 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.http://dx.doi.org/10.1155/2019/8249061
spellingShingle Yuji Naito
Tsukasa Miyatake
Manami Iwasaki
Atsushi Okuyama
Akio Takada
Koji Chiba
Masahiko Obata
Junichi Oba
Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications
Case Reports in Vascular Medicine
title Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications
title_full Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications
title_fullStr Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications
title_full_unstemmed Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications
title_short Rare Clinical Course of Immunoglobulin G4-Related Inflammatory Abdominal Aortic Aneurysm with Multiple Rare Complications
title_sort rare clinical course of immunoglobulin g4 related inflammatory abdominal aortic aneurysm with multiple rare complications
url http://dx.doi.org/10.1155/2019/8249061
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