A rare case: IgG4‐related chronic inflammatory disease with kidney involvement

Author:

Mete Fatos1,Mengeneci Tuba1ORCID,Albayrak Emre1,Ayar Yavuz2ORCID,Nalbant Melike3,Ozudeniz Mutlucan Ilknur4ORCID,Fusun Baba Zeliha5

Affiliation:

1. Department of Internal Medicine Bursa City Hospital Bursa Turkey

2. Division of Nephrology, Department of Internal Medicine Bursa City Hospital Bursa Turkey

3. Department of Medical Pathology Bursa City Hospital Bursa Turkey

4. Department of Radiology Bursa City Hospital Bursa Turkey

5. Department of Medical Pathology Acıbadem International Hospital Istanbul Turkey

Abstract

AbstractIgG4‐related disease is an inflammatory, multisystemic disease that affects the immune system. The disease progresses to fibrosis due to inflammation. Retroperitoneal fibrosis is a serious complication. Pancreas, biliary tract, glands, thyroid, lymph nodes, etc. may be involved. Prognosis is usually subacute, and seen in middle age and advanced men. It is characterized histopathologically by IgG4 positive plasma cells, lymphoplasmocytic cell infiltration, and storiform fibrosis. In our case, we evaluated a patient who referred to our clinic from an external center with the complaints of generalized pain, itching, tearing and redness in eyes, involvement of bilateral large joints, and impaired renal function. Diagnosis, treatment and management of the disease are important. Response to glucocorticoid therapy is good.

Publisher

Wiley

Subject

General Medicine

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