Results 51 to 60 of about 39,270 (221)

Management of Autoimmune Pancreatitis [PDF]

Clinical Gastroenterology and Hepatology, 2019
The article contains modern data on such a chronic pancreatic disease as autoimmune pancreatitis (AIP). Statistical data on the prevalence and incidence of AIP are presented, the current international classification of this pathology is considered, the main features of type 1 AIP (lymphoplasmacytic sclerosing pancreatitis, LPSP) and type 2 AIP ...
Venkata S, Akshintala, Vikesh K, Singh
openaire   +3 more sources

Mass-forming type 2 autoimmune pancreatitis with upstream dilatation of the main pancreatic duct dilatation: a case report

Journal of Medical Case Reports
Background Type 2 autoimmune pancreatitis is characterized by multiple or segmental strictures of the main pancreatic duct without upstream dilatation.
Noriyuki Tagai, Takanori Goi, Kenji Koneri, Makoto Murakami   +3 more
doaj   +1 more source

Autoimmune Pancreatitis Type II: First Report from India [PDF]

Journal of Clinical and Diagnostic Research, 2017
Autoimmune Pancreatitis (AIP) presents in two forms - Type I or lymphoplasmacytic sclerosing pancreatitis and Type II or idiopathic ducto-centric pancreatitis (IDCP). AIP II is rare in south Asia and, especially so, in India.
Gunjan Desai, Prasad Pande, Chandralekha Tampi, Prasad Wagle   +3 more
doaj   +1 more source

An unusual case of autoimmune pancreatitis presenting as pancreatic mass and obstructive jaundice: a case report and review of the literature

Journal of Medical Case Reports, 2011
Background Autoimmune pancreatitis is a rare chronic inflammatory pancreatic disease that is increasingly being diagnosed worldwide. As a result of overlap in clinical and radiological features, it is often misdiagnosed as pancreatic cancer.
Conley Barbara A, Minter Rebecca M, Kotaru Veera-Pavan, Cuison Reuben V, Makol Ashima, Efeovbokhan Nephertiti, Chandana Sreenivasa R   +6 more
doaj   +1 more source

The Diagnostic Challenges of Autoimmune Pancreatitis

Case Reports in Gastroenterology, 2015
Autoimmune pancreatitis is a rare but important differential diagnosis from pancreatic cancer. This autoimmune disease can mimic pancreatic cancer by its clinical symptoms, including weight loss and jaundice.
Kata Papp, Eliane Angst, Stefan Seidel, Renata Flury-Frei, Franc Heinrich Hetzer   +4 more
doaj   +1 more source

Association of Childhood Acute Leukemia With Autoimmune Diseases

International Journal of Cancer, EarlyView.
A possible link exists between various pediatric autoimmune diseases (AIDs) and increased risk of childhood leukemia. Although immune dysregulation is a key feature of these conditions, the connection between them remains unclear. In this study, using cancer registry data in Finland, the authors examined associations between AIDs and childhood acute ...
Ida Pellikka, Julia Ventelä, Anssi Auvinen, Olli Lohi, Atte Nikkilä   +4 more
wiley   +1 more source

Autoimmune pancreatitis diagnosis based on immunoglobulin G4 levels: Case report

Revista de la Facultad de Medicina, 2021
Introduction: Autoimmune pancreatitis is a rare form of chronic pancreatitis, with an estimated prevalence of 1 case per 100 000 inhabitants in the general population.
Lina Acosta-Buitrago, Akram Kadamani , Daniel Jiménez-González, Paulo Cabrera , Carlos Pérez-Rivera   +4 more
doaj   +1 more source

Oral Cryptococcosis due to Naganishia diffluens in a Patient With Thalassemia: A Case Report and a Literature Review

Journal of Clinical Laboratory Analysis, EarlyView.
Naganishia diffluens, a rare non‐neoformans cryptococcal species, was identified by PCR sequencing as the causative agent of oral cryptococcosis in a 31‐year‐old Iranian man with β‐thalassemia. This case represents the first documented instance of oral infection by N.
Zahra Yahyazadeh, Zeynab Haseli, Javad Javidnia, Mahdi Abastabar, Eisa Nazar, Hosein Jalali, Mohamad Taghi Hedayati, Hossein Karami, Mohsen Nosratabadi, Lotfollah Davoodi, Seyyed Reza Aghili, Maryam Moazeni, Iman Haghani, Hamid Badali   +13 more
wiley   +1 more source

Autoimmune Pancreatitis Exhibiting Multiple Mass Lesions

Case Reports in Gastroenterology, 2011
Our case is a first report of autoimmune pancreatitis with multiple masses within the pancreas which was pathologically diagnosed by endoscopic ultrasound-guided fine needle aspiration and treated by steroid.
Masahiro Shiokawa, Yuzo Kodama, Yukiko Hiramatsu, Akira Kurita, Yugo Sawai, Norimitsu Uza, Tomohiro Watanabe, Tsutomu Chiba   +7 more
doaj   +1 more source

Long‐Term Outcomes and Predictors of Delayed Steroid Initiation in Type 1 Autoimmune Pancreatitis Initially Managed Without Corticosteroids

Journal of Hepato-Biliary-Pancreatic Sciences, EarlyView.
ABSTRACT Background/Purpose Although type 1 autoimmune pancreatitis (AIP) responds well to corticosteroids, spontaneous remission can also occur. This study evaluated long‐term outcomes and predictors of delayed steroid initiation in AIP patients initially managed conservatively.
Yasuhiro Kuraishi, Akira Nakamura, Masafumi Minamisawa, Takumi Yanagisawa, Chinatsu Yonekura, Nobukazu Sasaki, Shunsuke Imamura, Takefumi Kimura, Yugo Iwaya, Tadanobu Nagaya   +9 more
wiley   +1 more source