Subclinical renal involvement in essential cryoglobulinemic vasculitis and classic polyarteritis nodosa
Autor: | Mohamed M. NasrAllah, Nermeen Khairy, Tamer A. Gheita, Hani Hussein |
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Rok vydání: | 2012 |
Předmět: |
Adult
Male Vasculitis medicine.medical_specialty Pathology Neutrophils Biopsy Fluorescent Antibody Technique Kidney urologic and male genital diseases Gastroenterology Glomerulonephritis Rheumatology Internal medicine Membranoproliferative glomerulonephritis Humans Medicine Outpatient clinic Autoantibodies Subclinical infection medicine.diagnostic_test business.industry Middle Aged medicine.disease Cryoglobulinemia Polyarteritis Nodosa Female Renal biopsy business Systemic vasculitis |
Zdroj: | Joint Bone Spine. 79:274-280 |
ISSN: | 1297-319X |
DOI: | 10.1016/j.jbspin.2011.06.009 |
Popis: | Objective Renal vasculitis is usually associated with anti-neutrophil cytoplasmic antibodies (ANCAs). However, non-ANCA patients constitute a rarely studied variant of renal vasculitis. The aim of the present study was to demonstrate the features of renal involvement in patients with primary systemic non-ANCA associated vasculitis (NAAV) and compare essential cryoglobulinemic vasculitis (ECV) with classic polyarteritis nodosa (PAN). Methods The study included 30 patients with primary systemic non-ANCA associated vasculitis (NAAV). Fifteen with ECV and another 15 patients with classic PAN. The patients were recruited from the Rheumatology and Internal medicine departments and outpatient clinics of Cairo University Hospitals. The patients had no or mild renal involvement at entry and the ANCA was negative as tested by immunoflourescence and ELISA. Renal biopsy was performed for all the patients and histopathologically studied. Results Renal biopsy abnormalities were seen in six females. One patient with PAN showed renal vasculitis and membranoproliferative glomerulonephritis (MPGN) and was HBV and ANA positive. The patient had negative HCV and cryoglobulins. Five patients with ECV-associated HCV had findings; one had chronic interstitial nephritis and was HBV positive. The other four were HBV negative with MPGN in two, focal proliferative and crescentic GN in one patient each. Conclusions Increased understanding of the manifestations of systemic vasculitis is likely to provide the basis for the use of more selective immunomodulatory therapies in the future. It is our hope that this study will raise awareness of the non ANCA-associated vasculitic renal involvement. |
Databáze: | OpenAIRE |
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