Results 91 to 100 of about 23,206 (196)
Pathophysiology of autoimmune pancreatitis
Autoimmune pancreatitis (AIP) is a recently discovered form of pancreatitis and represents one of the diseases of the pancreas which can be cured and healed medically. International consensus diagnostic criteria have been developed, and the clinical phenotypes associated with the histopathologic patterns of lymphoplasmacytic sclerosing pancreatitis and
Raffaele, Pezzilli, Nico, Pagano
openaire +2 more sources
ABSTRACT Systemic lupus erythematosus (SLE) can rarely present as concurrent acute pancreatitis (AP), splenic infarction, and renal failure. This case demonstrates that prompt diagnosis and immunosuppression are crucial for reversing organ damage—even in male patients, expanding the known clinical spectrum of this disease.
Jian‐mei Gong, Xu Jun
wiley +1 more source
Salivary Extracellular Vesicles: Paradigm Shift in Liquid Biopsy Diagnostics
ABSTRACT Extracellular vesicles (EVs), lipid bilayer nanoparticles released by virtually all cells, serve as essential messengers for intercellular communication. Due to their involvement in several pathophysiological processes, EVs have recently gained considerable attention as potentially diagnostic and prognostic biomarkers for various illnesses ...
Kwanele Xulu +3 more
wiley +1 more source
Necrotising pancreatitis is a severe and life-threatening form of acute pancreatitis characterised by the necrosis of pancreatic and peripancreatic tissues due to intense inflammation and autodigestion.
Antonio Al Hazzouri +6 more
doaj +1 more source
We report a series of 12 patients (mean age 63 years) with chronic oesophageal ulceration showing morphological features of IgG4‐related inflammatory disease. Most patients underwent several rounds of endoscopy until this association was recognized. The majority of patients went into clinical and histological remission following corticosteroid therapy.
Hanna Henzinger +5 more
wiley +1 more source
ABSTRACT Background We aimed to investigate and characterise DILI due to approved therapies for inflammatory bowel disease (IBD). Methods Using the Drug‐Induced Liver Injury Network (DILIN) prospective study, we evaluated definite, highly likely, or probable DILI attributed to IBD therapies, including use for non‐IBD indications (but excluding ...
Harish Gopalakrishna +9 more
wiley +1 more source
A Three‐Step Diagnostic Strategy for Malignant Pleural Effusions
ABSTRACT New diagnostic tools, such as high fluorescence cells (HFc) and tumor markers (TMs), have emerged in the quest to accurately diagnose malignant pleural effusion (MPE). This study evaluated the diagnostic performance of the HFc and TMs combination.
Elisa Nuez‐Zaragoza +17 more
wiley +1 more source
ABSTRACT Drug‐induced liver injury (DILI) remains a diagnosis of exclusion and requires systematic causality assessment. Meropenem is generally considered hepatically safe; however, rare cases of idiosyncratic DILI have been reported. We describe a 33‐year‐old female who developed progressive elevation of liver tests following exposure to meropenem ...
Nidal Mutawodeh +6 more
wiley +1 more source
ABSTRACT Methotrexate (MTX) is a folate antagonist widely used as a disease‐modifying antirheumatic drug (DMARD) in rheumatoid arthritis (RA), as well as in several malignancies and autoimmune disorders. Although low‐dose MTX (5–20 mg/week) is generally considered safe, it has a narrow therapeutic index, and toxicity can occur even at therapeutic doses,
Fatemeh Afra +7 more
wiley +1 more source
A Rare Presentation of Granulomatosis With Polyangiitis: A Case Report and Literature Review
ABSTRACT Granulomatosis with polyangiitis (GPA) is a rare ANCA‐associated necrotizing vasculitis that predominantly affects the respiratory tract and kidneys. Gastrointestinal involvement is uncommon, and pancreatic manifestations are exceedingly rare. Diffuse alveolar hemorrhage (DAH) represents a severe and potentially fatal complication. We report a
Anil Shahi +2 more
wiley +1 more source

