Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913577PMC
http://dx.doi.org/10.3238/arztebl.2018.0181DOI Listing

Publication Analysis

Top Keywords

igg4-associated inflammatory
4
inflammatory pseudotumor
4
pseudotumor bilobar
4
bilobar hepatic
4
hepatic foci
4
igg4-associated
1
pseudotumor
1
bilobar
1
hepatic
1
foci
1

Similar Publications

Background: Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis that presents clinically with obstructive icterus, histologically with infiltration of pancreatic parenchyma by inflammatory cells leading to chronic inflammation with fibrosis, and therapeutically with good response to corticosteroid therapy. Clinically, it may resemble malignant disease, making diagnosis difficult and requiring a multidisciplinary team (gastroenterologist, endoscopist, radiologist, surgeon, pathologist). Two types of AIP are distinguished.

View Article and Find Full Text PDF

IgG4-related sclerosing cholangitis (IgG4-SC) is an inflammatory disease that leads to bile duct stricture, characterized by the infiltration of IgG4-positive plasma cells into the bile duct wall, thickening of the bile duct wall, and narrowing of the lumen. The differential diagnosis of IgG4-SC mainly includes primary sclerosing cholangitis, cholangiocarcinoma, and pancreatic cancer. IgG4-SC is often associated with autoimmune pancreatitis and can be accurately diagnosed based on clinical diagnostic criteria.

View Article and Find Full Text PDF

Background: Idiopathic retroperitoneal fibrosis is characterized by the development of inflammatory infiltrates with marked fibrosis along the large retroperitoneal vessels. Rituximab in combination with glucocorticoids constitute an effective therapy, but the responses are not long-lasting. In other similar situations, addition of cyclophosphamide to the combination achieved longer and deeper responses.

View Article and Find Full Text PDF
Article Synopsis
  • A 49-year-old man visited the emergency department with symptoms including weight loss, abdominal pain, and elevated inflammatory markers, leading to the discovery of a large liver tumor and swollen bile ducts.
  • The tumor raised concerns for intrahepatic cholangiocarcinoma, prompting surgical procedures including segmental hepatectomy and lymphadenectomy.
  • Post-surgery analysis revealed the tumor was an IgG4-associated disease, and the patient showed positive recovery without any recurrence of symptoms.
View Article and Find Full Text PDF
Article Synopsis
  • Idiopathic granulomatous mastitis (IGM) is a chronic, non-cancerous breast condition, and this study focused on the impact of steroid treatment on tissue levels of Immunoglobulin G4 (IgG4) in patients with IGM.
  • The study analyzed data from 55 patients diagnosed with IGM, categorizing them into three groups based on their tissue IgG4 levels, with varying response rates to steroid treatment: 77.8% for Group I (negative IgG4), 91.3% for Group II (slightly positive), and an initial 95.65% for Group III (highly positive) but with a relapse rate of 26.1% after treatment stopped.
View Article and Find Full Text PDF