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A case of immunotactoid glomerulopathy with rapid progression to end-stage renal disease
Shikha Jain1, Darshika Chhabra
1Department of Internal Medicine, University of Illinois, Chicago, USA. sjain03@gmail.com
Abstract:
Immunotactoid glomerulopathy (IGN) is a rare immunoglobulin deposition disease. It is often mistaken for cryoglobulinemia or amyloidosis due to the similarities on biopsy findings. The disease progresses to end-stage renal disease (ESRD) within 7 months to 10 years. This is the first case reported of a patient with a diagnosis of IGN who developed acute kidney injury (AKI) and ESRD within 1 week of initial presentation.
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