Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience
© JOURNAL OF THE MEDICAL ASSOCIATION OF THAILAND| 2020 Background: Autoimmune pancreatitis (AIP) and IgG4-related cholangitis (IRC) are newly-recognized diseases. Reports in Thailand are scarce. Objective: To evaluate clinical presentations, other organ involvement (OOI), serology, radiologic, endos...
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th-mahidol.605182020-12-28T13:01:06Z Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience Kritsanat Lertussavavivat Sasamon Chumjang Supot Pongprasobchai Faculty of Medicine, Siriraj Hospital, Mahidol University Medicine © JOURNAL OF THE MEDICAL ASSOCIATION OF THAILAND| 2020 Background: Autoimmune pancreatitis (AIP) and IgG4-related cholangitis (IRC) are newly-recognized diseases. Reports in Thailand are scarce. Objective: To evaluate clinical presentations, other organ involvement (OOI), serology, radiologic, endoscopic features and treatment of AIP and IRC in one institute. Materials and Methods: Patients with AIP and IRC, who were diagnosed and followed-up at Siriraj Hospital during 2005 to 2016 were retrospectively reviewed. Results: There were 15 patients (75%) with AIP, 7 patients (37%) with IRC (4 isolated IRC and 3 IRC with AIP) and 1 (5%) with IgG4-related disease without AIP or IRC (sialadenitis and retroperitoneal fibrosis). Male to female ratio was 1.9: 1. Median age of onset was 64 years. Among the 15 AIP, all were type 1. Initial presentations were jaundice (60%), abdominal pain (40%), OOI (20%; sialadenitis, orbital pseudotumor), and weight loss (7%). Clinical manifestations during the course were jaundice (80%), abdominal pain (67%), weight loss (47%), OOI (47%; retroperitoneal fibrosis, IRC, sialadenitis, orbital pseudotumor, periurethral mass, lung nodules) and steatorrhea (7%). Serum IgG4 was elevated in all patients. Radiography showed diffuse type in 8 cases (53%), focal type in 5 (33%), and unknown in 2 (13%). More than half were suspicious of AIP before diagnosis. Corticosteroid was required in 10 patients (67%). Maintenance therapy was offered in 5 patients (33%) with steroid and azathioprine. Surgery was performed before diagnosis in 7 patients (47%). Spontaneous remission occurred in 4 patients (27%). Among the 7 IRC, initial presentations were jaundice (57%), weight loss (29%), abdominal pain (14%), prolonged fever (14%), and cholangitis (14%). Clinical manifestations during the course were jaundice (57%), abdominal pain (57%), weight loss (29%), recurrent cholangitis (14%) and retroperitoneal fibrosis (14%). Serum IgG4 was elevated in 5 patients (71%). Prednisolone was prescribed in 6 cases (86%). Five patients (71%) required azathioprine. Surgery was performed before diagnosis in 4 patients (57%). Conclusion: AIP and IRC were uncommon. The most common presentation was jaundice. All AIP were type 1 and more than half were diffuse type. OOI were common. Half of IRC had AIP. Approximately half of AIP/IRC patients underwent surgery before diagnosis. Corticosteroid was mainstay treatment. 2020-12-28T06:01:06Z 2020-12-28T06:01:06Z 2020-12-01 Article Journal of the Medical Association of Thailand. Vol.103, No.12 (2020), S58-S63 10.35755/jmedassocthai.2020.S08.12173 01252208 2-s2.0-85097610969 https://repository.li.mahidol.ac.th/handle/123456789/60518 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85097610969&origin=inward |
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Medicine Kritsanat Lertussavavivat Sasamon Chumjang Supot Pongprasobchai Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience |
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© JOURNAL OF THE MEDICAL ASSOCIATION OF THAILAND| 2020 Background: Autoimmune pancreatitis (AIP) and IgG4-related cholangitis (IRC) are newly-recognized diseases. Reports in Thailand are scarce. Objective: To evaluate clinical presentations, other organ involvement (OOI), serology, radiologic, endoscopic features and treatment of AIP and IRC in one institute. Materials and Methods: Patients with AIP and IRC, who were diagnosed and followed-up at Siriraj Hospital during 2005 to 2016 were retrospectively reviewed. Results: There were 15 patients (75%) with AIP, 7 patients (37%) with IRC (4 isolated IRC and 3 IRC with AIP) and 1 (5%) with IgG4-related disease without AIP or IRC (sialadenitis and retroperitoneal fibrosis). Male to female ratio was 1.9: 1. Median age of onset was 64 years. Among the 15 AIP, all were type 1. Initial presentations were jaundice (60%), abdominal pain (40%), OOI (20%; sialadenitis, orbital pseudotumor), and weight loss (7%). Clinical manifestations during the course were jaundice (80%), abdominal pain (67%), weight loss (47%), OOI (47%; retroperitoneal fibrosis, IRC, sialadenitis, orbital pseudotumor, periurethral mass, lung nodules) and steatorrhea (7%). Serum IgG4 was elevated in all patients. Radiography showed diffuse type in 8 cases (53%), focal type in 5 (33%), and unknown in 2 (13%). More than half were suspicious of AIP before diagnosis. Corticosteroid was required in 10 patients (67%). Maintenance therapy was offered in 5 patients (33%) with steroid and azathioprine. Surgery was performed before diagnosis in 7 patients (47%). Spontaneous remission occurred in 4 patients (27%). Among the 7 IRC, initial presentations were jaundice (57%), weight loss (29%), abdominal pain (14%), prolonged fever (14%), and cholangitis (14%). Clinical manifestations during the course were jaundice (57%), abdominal pain (57%), weight loss (29%), recurrent cholangitis (14%) and retroperitoneal fibrosis (14%). Serum IgG4 was elevated in 5 patients (71%). Prednisolone was prescribed in 6 cases (86%). Five patients (71%) required azathioprine. Surgery was performed before diagnosis in 4 patients (57%). Conclusion: AIP and IRC were uncommon. The most common presentation was jaundice. All AIP were type 1 and more than half were diffuse type. OOI were common. Half of IRC had AIP. Approximately half of AIP/IRC patients underwent surgery before diagnosis. Corticosteroid was mainstay treatment. |
author2 |
Faculty of Medicine, Siriraj Hospital, Mahidol University |
author_facet |
Faculty of Medicine, Siriraj Hospital, Mahidol University Kritsanat Lertussavavivat Sasamon Chumjang Supot Pongprasobchai |
format |
Article |
author |
Kritsanat Lertussavavivat Sasamon Chumjang Supot Pongprasobchai |
author_sort |
Kritsanat Lertussavavivat |
title |
Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience |
title_short |
Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience |
title_full |
Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience |
title_fullStr |
Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience |
title_full_unstemmed |
Autoimmune Pancreatitis and IgG4-related Cholangitis: A Single-center Experience |
title_sort |
autoimmune pancreatitis and igg4-related cholangitis: a single-center experience |
publishDate |
2020 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/60518 |
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1763495688269725696 |