Results: 9

IgG4-related disease associated with immune thrombocytopenia: A clinical case report

Rev. colomb. reumatol; 29 (4), 2022
Autoimmune pancreatitis is a characteristic manifestation of the spectrum of the disease related to IgG4, a rare autoimmune disorder that presents clinically with obstructive jaundice due to the infiltration of plasma cells and fibrosis in the pancreas. There may be other symptoms in case of involvement ...

Enfermedad relacionada con IgG4: reporte de un caso y revisión de la literatura

Rev. méd. Maule; 36 (2), 2021
Immunoglobulin G4 (IgG4-RD) -related disease is a regional or systemic fibroinflammatory disease of unknown etiology. It has a characteristic histopathological appearance of dense lymphoplasmacytic infiltrates with abundant IgG4 positive plasma cells, storiform fibrosis and obliterative phlebitis with th...

Pancreatitis autoinmune en pediatría. Caso clínico

Arch. argent. pediatr; 119 (3), 2021
La pancreatitis recurrente ocurre en el 15-35% en la edad pediátrica. Se define como 2 o más episodios distintos de pancreatitis aguda con normalización de enzimas pancreáticas entre cada episodio. Una de sus causas es la pancreatitis autoinmune. En los últimos 10 años se contro...

Type 1 autoimmune pancreatitis: relapse with liver abscess

ABSTRACT: Type 1 autoimmune pancreatitis is a cause of chronic pancreatitis related to the systemic disease known as IgG4-related Sclerosing Disease. Case report: We report the case of a 64-year-old male patient who presented recurrentepigastric pain radiating to the ...

Diabetes mellitus asociada a pancreatitis autoinmune: caso clínico

Rev. méd. Chile; 147 (5), 2019
Autoimmune pancreatitis is uncommon, responds to steroids and is usually associated with diabetes mellitus. We report a 73 year-old male who, two months after a diagnosis of diabetes mellitus, presented with obstructive jaundice and weight loss. Abdominal magnetic resonance imaging was suggestive of an a...

Enfermedad por IgG4 multisistémica: a propósito de un caso: revisión de la literatura

Gastroenterol. latinoam; 30 (3), 2019
We report a 63-year-old male patient who consulted for a 4-month history of xerophthalmia, xerostomia and cervicalgia, associated with jaundice, choluria, low weight and night sweats. Exams show an obstructive pattern and abdominal ultrasound describes a possible mass in the pancreatic head with secondar...

Espectro clínico de la enfermedad relacionada con IgG4 en Colombia

Rev. colomb. reumatol; 25 (1), 2018
RESUMEN La enfermedad relacionada con IgG4 es una condición inflamatoria sistémica, caracterizada por la infiltración de diversos órganos por complejos formados por células plasmáticas IgG4 positivas, asociadas con niveles elevados de IgG4 en el suero. El diagnóstico de esta enfermedad es complejo...

Pancreatitis autoinmune: desafío diagnóstico y tratamiento actual

Gastroenterol. latinoam; 28 (supl.1), 2017
Autoimmune pancreatitis (AIP) is an inflammatory disease of the pancreas. The mechanism of the disease is not completely known. However, AIP shows cellular and humoral immunity elements, the most important being helper and regulatory T lymphocytes as well as B-lymphocytes and plasmocytes, participating i...

Doença sistêmica associada à IgG4, mimetizando colangiocarcinoma

A doença sistêmica associada à IgG4 pode acometer virtualmente todos os órgãos, o que torna seu diagnóstico diferencial bastante abrangente. A pancreatite autoimune foi a primeira lesão orgânica a ser associada à IgG4 e, apenas em 2003, manifestações extrapancreáticas foram descritas. Portant...