An unusual association between familial Mediterranean fever and IgM nephropathy
dc.contributor.author | Peru, Harun | |
dc.contributor.author | Elmaci, Ahmet Midhat | |
dc.contributor.author | Akin, Fatih | |
dc.contributor.author | Akcoren, Zuhal | |
dc.contributor.author | Orhan, Diclehan | |
dc.date.accessioned | 2020-03-26T17:26:24Z | |
dc.date.available | 2020-03-26T17:26:24Z | |
dc.date.issued | 2008 | |
dc.department | Selçuk Üniversitesi | en_US |
dc.description.abstract | Objective: To report a case with the diagnosis of IgM nephropathy and familial Mediterranean fever (FMF). Clinical Presentation and Intervention: A 9-year-old boy was admitted to our hospital with recurrent abdominal pain since the age of 4 years. Laboratory investigations revealed a sedimentation rate of 88 mm/h, C-reactive protein: 83.2 mg/l (0-10 mg/l), white blood cell count: 12,700/mm(3), fibrinogen: 622 mg/dl (200-400 mg/dl) and serum amyloid A: 186 mg/l (0-5.8 mg/l). Urinalysis revealed +2 proteinuria. A 24-hour urinary protein excretion was 12 mg/m(2)/h. M694V homozygous mutation was identified in exon 10. Percutaneous renal biopsy showed mesangial cell proliferation and increased mesangial matrix in the glomeruli, without amyloid accumulation. Immunofluorescence study showed IgM (+1) and C1q (+1) deposits. Treatment with 1 mg/day colchicine was started. Six weeks later, proteinuria had disappeared and the patient was asymptomatic. Conclusion: This case illustrates the unusual association of FMF with non-amyloid glomerulopathy. Glomerular diseases such as IgM nephropathy may be seen as a manifestation of FMF. Copyright (C) 2008 S. Karger AG, Basel. | en_US |
dc.identifier.doi | 10.1159/000117803 | en_US |
dc.identifier.endpage | 257 | en_US |
dc.identifier.issn | 1011-7571 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 18408398 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 255 | en_US |
dc.identifier.uri | https://dx.doi.org/10.1159/000117803 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12395/22204 | |
dc.identifier.volume | 17 | en_US |
dc.identifier.wos | WOS:000254894400015 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | KARGER | en_US |
dc.relation.ispartof | MEDICAL PRINCIPLES AND PRACTICE | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.selcuk | 20240510_oaig | en_US |
dc.subject | familial Mediterranean fever | en_US |
dc.subject | glomerulonephritis | en_US |
dc.subject | IgM nephropathy | en_US |
dc.title | An unusual association between familial Mediterranean fever and IgM nephropathy | en_US |
dc.type | Article | en_US |