IgG4-related sclerosing mesenteritis, a rare condition that causes abdominal pain
نویسندگان
چکیده
منابع مشابه
IgG4-Related Sclerosing Mesenteritis
© 2016 The Korean Society of Pathologists/The Korean Society for Cytopathology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. pISSN 2383-7...
متن کاملIgG4-related sclerosing mesenteritis causing bowel obstruction: a case report
Sclerosing mesenteritis (SM) is a rare inflammatory and fibrosing disease primarily involving the small-bowel mesentery. Recently, SM was reported to be closely related to IgG4-related disease (IgG4-RD). This report describes a patient with SM associated with IgG4-RD. A 77-year-old woman with a history of surgery for ectopic pregnancy and wound dehiscence presented with intestinal obstruction. ...
متن کاملA rare and emerging entity: Sinonasal IgG4–related sclerosing disease
BACKGROUND Immunoglobulin G4 (IgG4) related sclerosing disease (rSD) is a new disease entity, first described in 2001, that involves autoimmune pancreatitis. Considered a systemic disease with lesions described in multiple organ systems, IgG4-rSD that affects the sinonasal region is rare. Our goal was to highlight the sinonasal presentation of this unique disease and to review previously report...
متن کاملSclerosing mesenteritis as a rare cause of abdominal pain and intraabdominal mass: a cases report and review of the literature
Sclerosing mesenteritis is a rare, benign, and chronic fibrosing inflammation disease with unknown etiology that affects the mesentery of small bowel and colon. The disease has two well-established histological types: the acute or subacute form known as mesenteric panniculitis and the chronic form known as retractile or sclerosing mesenteritis. Because the sclerosing mesenteritis is lack of spe...
متن کاملIgG4-related sclerosing disease.
Based on histological and immunohistochemical examination of various organs of patients with autoimmune pancreatitis (AIP), a novel clinicopathological entity of IgG4-related sclerosing disease has been proposed. This is a systemic disease that is characterized by extensive IgG4-positive plasma cells and T-lymphocyte infiltration of various organs. Clinical manifestations are apparent in the pa...
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ژورنال
عنوان ژورنال: Revista Española de Enfermedades Digestivas
سال: 2017
ISSN: 1130-0108
DOI: 10.17235/reed.2017.5228/2017