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A Rare Presentation of Familial Mediterranean fever; Acute Scrotum and Hydrocele Amyloidosis
BACKGROUND: Familial Mediterranean Fever (FMF) is a genetic disease characterized by recurrent febrile attacks and inflammation of serous membranes. Amyloidosis is frequent in untreated FMF patients and is also the most important complication of FMF. It is generally seen with renal, hepatic, gastroi...
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| Main Authors: | , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Tehran University of Medical Sciences
2010
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3446044/ https://ncbi.nlm.nih.gov/pubmed/23056732 |
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