Recognizing isolated IgG4-related nephropathy
Autor: | Rabya Sayed, A. Palmer, Terence Cook |
---|---|
Rok vydání: | 2013 |
Předmět: |
Transplantation
Pathology medicine.medical_specialty Kidney Systemic disease Clinical Report business.industry fungi IgG4-related systemic disease medicine.disease Tubulointerstitial Nephritis Nephropathy medicine.anatomical_structure isolated renal involvement Nephrology Immunoglobulin g4 parasitic diseases Clinical Cases Medicine Organ involvement tubulointerstitial nephritis skin and connective tissue diseases business |
Zdroj: | Clinical Kidney Journal |
ISSN: | 2048-8513 2048-8505 |
DOI: | 10.1093/ckj/sfs187 |
Popis: | IgG4-related tubulointerstitial nephritis is an uncommon cause of renal impairment. It has been associated with dysfunction in a number of other organs giving rise to the term IgG4-related systemic disease; organ involvement can occur metachronously, hence, making it more difficult to identify patients. The exact cause of this condition remains unknown. Here, we present a case of isolated renal involvement which demonstrates how particular biochemical, radiological and histopathological changes should raise the suspicion of IgG4-related nephropathy, especially when there is an absence of clues from any other organ. |
Databáze: | OpenAIRE |
Externí odkaz: |