| Literature DB >> 19711078 |
Hamdi Emeksiz1, Sevcan Bakkaloglu, Orhun Camurdan, Mehmet Boyraz, Oguz Soylemezoglu, Enver Hasanoglu, Necla Buyan.
Abstract
The most devastating complication of familial Mediterranean fever (FMF) is amyloidosis which is capable of resulting in chronic renal failure. Although amyloid deposits are frequent in adrenal glands based on the autopsies of FMF patients however; to our knowledge, symptomatic adrenal insufficiency has not been reported yet. We describe a 21-year-old-FMF amyloidosis case with a well-functioning allograft who presented to the emergency clinic with the complaints of abdominal pain, vomiting and diarrhea mimicking FMF attack. adrenocorticotrophic hormone stimulation test was performed due to resistant hyponatremia and disclosed Addison disease. In countries with a high prevalence of FMF, adrenal crisis should be borne in mind in long standing FMF patients.Entities:
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Year: 2009 PMID: 19711078 DOI: 10.1007/s00296-009-1115-0
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631