Inflammatory Fibroid Polyps: A Systematic Review Focusing on Genetics
1. Abstract 1.1. Background: This study will review IFP (inflammatory fibroid polyp) by analyzing both sporadic and familial cases with a genetics- focused approach.
1. Abstract 1.1. Background: This study will review IFP (inflammatory fibroid polyp) by analyzing both sporadic and familial cases with a genetics- focused approach.
1. Abstract 1.1. Background: Pancreatic fibrosis has also been found to occur in association with insulin insufficiency and pancreatic ductal adenocarcinoma. It is important to investigate the development, progression and causal factors of fibrosis.
1. Abstract Enteritis as the only manifestation of (COVID-19) in adolescents without features of multisystem syndrome in children (MIS-C) or a prior history of inflammatory bowel disease (IBD) is presented.
1. Abstract 1.1. Background: SMARCB1/INI-1-deficient pancreatic carcinoma is a rarely reported entity. So far, only 10 cases have been published in the literature, and most of the reported cases have poor prognosis and mortality rate within six months is extremely high. The clinical presentation, histopathological features, and biologically behaviors are essentially unclear.
1. Abstract This case demonstrates a rare cause of acute pancreatitis secondary to migration of a gastrostomy tube into the descending part of the duodenum to cause pancreatic duct obstruction.
1. Abstract 1.1. Introduction: Determinants of mortality of patients with liver cirrhosis and septic shock are poorly known.
1. Clinical Image A 38-year-old bile prosthesis bearer, not anti-coagulated nor anti-aggregated, was subjected to an ERCP to move it away. A hard-working procedure was made so multiple attempts were needed. After it, the patient felt right lumbar pain and hemoglobin fall, developing hemorrhagic shock and requiring orotracheal intubation, blood components transfusion and use of …
1. Introduction Infectious esophagitis, including candida and HSV, often presents in the backdrop of systemic illness and an immunocompromised state, with dysphagia as a prominent symptom. Here, we describe a case of infectious esophagitis in the setting of neurosyphilis.
1. Case Report The igG4-related disease is a chronic relapsing multiorgan fibroinflammatory syndrome of autoimmune etiology [1], characterized by a distinctive histopathological pattern of IgG4 in affected tissues, imaging findings, increased serum IgG4 levels, synchronous multiorgan distress, and response to glucocorticoids.
1. Abstract Efferocytosis is the process by which phagocytes remove programmed dead cells, a process understood as the burial of apoptotic cells, hence the term “efferocytosis”.