Literature DB >> 20024509

A case of immunotactoid glomerulopathy with rapid progression to end-stage renal disease.

Shikha Jain1, Darshika Chhabra.   

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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Year:  2009        PMID: 20024509      PMCID: PMC5823090          DOI: 10.1100/tsw.2009.164

Source DB:  PubMed          Journal:  ScientificWorldJournal        ISSN: 1537-744X


  2 in total

1.  Recurrence of fibrillary glomerulonephritis in a renal transplant recipient.

Authors:  Ahmed Mitwalli; Iqbal Shah; Durdana Hammad; Hala Kafoury
Journal:  Int Urol Nephrol       Date:  2012-07-24       Impact factor: 2.370

2.  A case of membranoproliferative glomerulonephritis associated with curved fibril deposition.

Authors:  Ikuyo Narita; Michiko Shimada; Takeshi Fujita; Reiichi Murakami; Masayuki Nakamura; Norio Nakamura; Hideaki Yamabe; Ken Okumura
Journal:  BMC Nephrol       Date:  2015-09-15       Impact factor: 2.388

  2 in total

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