A case of giant retroperitoneal lymphangioma and IgG4-positive fibrosis: Causality or coincidence?
Abdominal cyst
IgG4-related disease
Ormond’s disease
acute kidney failure
lymphangioma
retroperitoneal fibrosis
Journal
SAGE open medical case reports
ISSN: 2050-313X
Titre abrégé: SAGE Open Med Case Rep
Pays: England
ID NLM: 101638686
Informations de publication
Date de publication:
2021
2021
Historique:
received:
22
11
2020
accepted:
21
04
2021
entrez:
7
6
2021
pubmed:
8
6
2021
medline:
8
6
2021
Statut:
epublish
Résumé
Several chronic inflammatory diseases have been found to be a subtype of IgG4-related disease, all of which have a typical clinical and histological change, which is based in particular on an overexpression of IgG4 and subsequent fibrosis. At least a part of the retroperitoneal fibrosis, which was originally classified as idiopathic, seems to be assigned to IgG4-related disease. Lymphangiomas are benign, cystic tumors that rarely occur in adults. However, there is no firm association with IgG4-related disease described in the literature to date. This report is about a patient suffering from acute renal failure due to a giant retroperitoneal cyst. Surgical resection remains incomplete in the iliac vessel area due to severe fibrosis and histology revealed features of both lymphangioma and IgG4
Identifiants
pubmed: 34094565
doi: 10.1177/2050313X211016993
pii: 10.1177_2050313X211016993
pmc: PMC8141978
doi:
Types de publication
Case Reports
Langues
eng
Pagination
2050313X211016993Informations de copyright
© The Author(s) 2021.
Déclaration de conflit d'intérêts
Declaration of conflicting interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
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