Results 161 to 170 of about 29,894 (207)

Acute-Onset Type 1 Diabetes in a Patient With Autoimmune Polyendocrine Syndrome Type 3A Following Influenza A Infection: A Case Report. [PDF]

Cureus
Doi S, Kenzaka T, Kiriishi N, Fujiwara R, Nishisaki H.   +4 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Autoimmune pancreatitis type 2 (idiopathic duct-centric pancreatitis): A comprehensive review

Journal of Autoimmunity, 2023
Autoimmune pancreatitis (AIP) is an uncommon fibro-inflammatory disorder precipitated by autoimmune/inflammatory reactions. Currently, there are two clinical subtypes of AIP (type 1 [AIP-1] and type 2 [AIP-2]) that correspond to two histologic descriptors (lymphoplasmacytic sclerosing pancreatitis and idiopathic duct-centric pancreatitis, respectively).
Yang Li, Hanyi Song, Xiangzhen Meng, Runzhuo Li, Patrick S.C. Leung, M. Eric Gershwin, Shucheng Zhang, Siyu Sun, Junmin Song   +8 more
openaire   +2 more sources

A case of type 2 autoimmune pancreatitis with spontaneous remission

Clinical Journal of Gastroenterology, 2023
A 70-year-old man with epigastric pain was referred to our hospital. Computed tomography and magnetic resonance imaging showed the diffusely enlarged pancreas compared to his normal pancreas 6 months prior to presentation. Serum levels of IgG4 and amylase were normal, while C-reactive protein was slightly elevated.
Takashi Ito, Tsukasa Ikeura, Kenji Notohara, Masataka Masuda, Koh Nakamaru, Shinji Nakayama, Masaaki Shimatani, Makoto Takaoka, Kazuichi Okazaki, Makoto Naganuma   +9 more
openaire   +2 more sources

Autoimmune Pancreatitis Type 2

American Journal of Surgical Pathology, 2019
Background: Autoimmune pancreatitis (AIP) encompasses a heterogenous disease group that includes IgG4-related type 1 AIP and non–IgG4-related type 2 AIP. Clinically and on imaging, type 2 AIP mimics type 1 AIP, other forms of chronic pancreatitis and pancreatic ductal adenocarcinoma (PDAC); therefore, discriminatory markers may
Rajib, Gupta, Azfar, Neyaz, Abhijit, Chougule, Masayuki, Akita, Yoh, Zen, David, Forcione, Carlos Fernandez-Del, Castillo, Cristina R, Ferrone, Vikram, Deshpande   +8 more
openaire   +2 more sources

Recent advances in autoimmune pancreatitis: type 1 and type 2

Gut, 2013
Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis characterised clinically by frequent presentation with obstructive jaundice, histologically by a lymphoplasmacytic infiltrate with fibrosis, and therapeutically by a dramatic response to steroids. When so defined, AIP can be sub-classified into two subtypes, 1 and 2.
Terumi, Kamisawa, Suresh T, Chari, Markus M, Lerch, Myung-Hwan, Kim, Thomas M, Gress, Tooru, Shimosegawa   +5 more
openaire   +2 more sources

Outcome of Patients With Type 1 or 2 Autoimmune Pancreatitis

American Journal of Gastroenterology, 2011
Autoimmune pancreatitis (AIP) is better described than before, but there is still no international consensus for definition, diagnosis, and treatment. Our aims were to analyze the short- and long-term outcome of patients with focus on pancreatic endocrine and exocrine functions, to search for predictive factors of relapse and pancreatic insufficiency ...
Frédérique, Maire, Yann, Le Baleur, Vinciane, Rebours, Marie Pierre, Vullierme, Anne, Couvelard, Hélène, Voitot, Alain, Sauvanet, Olivia, Hentic, Philippe, Lévy, Philippe, Ruszniewski, Pascal, Hammel   +10 more
openaire   +3 more sources

Republished: Recent advances in autoimmune pancreatitis: type 1 and type 2

Postgraduate Medical Journal, 2013
Abstract Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis characterised clinically by frequent presentation with obstructive jaundice, histologically by a lymphoplasmacytic infiltrate with fibrosis, and therapeutically by a dramatic response to steroids. When so defined, AIP can be sub-classified into two subtypes, 1 and 2.
Terumi, Kamisawa, Suresh T, Chari, Markus M, Lerch, Myung-Hwan, Kim, Thomas M, Gress, Tooru, Shimosegawa   +5 more
openaire   +2 more sources