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Immunoglobulin G4 Related Retroperitoneal Fibrosis with Acute Kidney Injury: Report of A Case / 대한신장학회지
Korean Journal of Nephrology ; : 519-524, 2010.
Article in Korean | WPRIM | ID: wpr-63647
ABSTRACT
Immunoglobuin G4 (IgG4)-related sclerosing disease is a recently recognized syndrome characterized clinically by male predominance, elevated serum IgG4 level, and good response to steroid therapy. The pathologic characteristics are extensive lymphoplasmacytic infiltration with IgG4-positive cell and irregular fibrosis in various organs (pancreas, bile duct, salivary gland, retroperitoneum, kidney and lung). Some inflammatory pseudotumors may be involved in this disease. Herein, we experienced a case of IgG4-related retroperitoneal fibrosis with postrenal acute kidney injury and inflammatory pseudotumor of thyroid in a 31-year-old female who underwent insertion of double J catheter at both ureters and received corticosteroid treatment.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Retroperitoneal Fibrosis / Salivary Glands / Thyroid Gland / Ureter / Bile Ducts / Fibrosis / Immunoglobulin G / Immunoglobulins / Acute Kidney Injury / Catheters Limits: Adult / Female / Humans / Male Language: Korean Journal: Korean Journal of Nephrology Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Retroperitoneal Fibrosis / Salivary Glands / Thyroid Gland / Ureter / Bile Ducts / Fibrosis / Immunoglobulin G / Immunoglobulins / Acute Kidney Injury / Catheters Limits: Adult / Female / Humans / Male Language: Korean Journal: Korean Journal of Nephrology Year: 2010 Type: Article