Title of article
Familial Mediterranean fever—a not so unusual cause of abdominal pain
Author/Authors
Anna Simon، نويسنده , , Jos W.M. van der Meer، نويسنده , , Joost P.H. Drenth، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
15
From page
199
To page
213
Abstract
Familial Mediterranean fever is a hereditary syndrome characterised by recurrent episodes of fever and serositis, resulting in pain in the abdomen, chest, joints and muscles. It is primarily diagnosed in people of Jewish, Arabic, Turkish or Armenian ancestry and is caused by mutations in the gene encoding for pyrin. Abdominal FMF attacks resemble the clinical presentation of ‘acute abdomen’, with severe abdominal pain and rigidity, but in FMF symptoms always resolve spontaneously. It is important to distinguish these regular pain episodes from small bowel obstruction due to adhesions to prevent life-threatening bowel strangulation. In most cases, colchicine will prevent new painful attacks. This seminar also discusses other causes of abdominal pain in FMF patients.
Keywords
Familial Mediterranean fever , Colchicine , autoinflammatory syndromes , acute abdomen , vasculitis.
Journal title
Best Practice and Research Clinical Gastroenterology
Serial Year
2005
Journal title
Best Practice and Research Clinical Gastroenterology
Record number
466499
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