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IgG4-Related Systemic Disease Can Be Easily Mistaken as a Uroepithelial Tumor / 전남의대학술지
Chonnam Medical Journal ; : 39-42, 2015.
Article in English | WPRIM | ID: wpr-133646
ABSTRACT
Immunoglobulin G4-related disease (IgG4-RD) is a newly recognized systemic syndrome characterized by elevated serum IgG4 concentrations and tumefaction or tissue infiltration by IgG4-positive plasma cells. We experienced a case of IgG4-RD involving multiple organs in a 64-year-old female who was referred for a suspected uroepithelial tumor. A mass biopsy confirmed dense lymphoplasmacytic infiltration with an increased number of IgG4-positive plasma cells. We discuss this case and review the literature to bring IgG4-RD to the attention to clinicians because it responds dramatically well to steroid therapy and should be kept in mind as a differential diagnosis to avoid unnecessary surgery.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Plasma Cells / Sclerosis / Biopsy / Immunoglobulin G / Immunoglobulins / Unnecessary Procedures / Diagnosis, Differential / Kidney Type of study: Diagnostic study Limits: Female / Humans Language: English Journal: Chonnam Medical Journal Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Plasma Cells / Sclerosis / Biopsy / Immunoglobulin G / Immunoglobulins / Unnecessary Procedures / Diagnosis, Differential / Kidney Type of study: Diagnostic study Limits: Female / Humans Language: English Journal: Chonnam Medical Journal Year: 2015 Type: Article