Familial Mediterranean fever
Key points
- Familial Mediterranean fever is an inherited disorder characterized by recurrent fever and inflammation, often involving the abdomen or the lung.
- The cause of familial Mediterranean fever is unknown.
- There is no specific test to diagnose this disease.
- There is no known cure for familial Mediterranean fever.
Alternative names
Familial paroxysmal polyserositis; Periodic peritonitis; Recurrent polyserositis; Benign paroxysmal peritonitis; Periodic disease; Periodic fever
Definition
Familial Mediterranean fever is an inherited disorder characterized by recurrent fever and inflammation, often involving the abdomen or the lung.
Causes, incidence, and risk factors
The cause of familial Mediterranean fever is unknown. It usually affects people of Mediterranean ancestry, especially non-Ashkenazi (Sephardic) Jews, Armenians, and Arabs, although people from other ethnic groups may also be affected.
Symptoms usually begin between age 5 and 15. Inflammation in the lining of the abdominal cavity, chest cavity, skin, or joints occurs, along with high fevers that usually peak in 12 to 24 hours. Attacks may vary in severity of symptoms, and people are usually symptom free between attacks.
This disease is very rare. Risk factors include a family history of familial Mediterranean fever or having Mediterranean ancestry.
Symptoms
- Fever or alternating chills and fever (relapsing)
- Abdominal pain
- Chest pain that occurs repeatedly (recurrent)
- Recurrent abdominal pain, recurrent
- Recurrent joint pain
o Pain in hip, knee, ankle, shoulder elbow or wrist
o Pain over the small joints of the foot or hand
o Pain in other joints - Skin lesions that are red and swollen and range from 5-20 cm in diameter
Signs and tests
There is no specific test to diagnose this disease. Sometimes analysis of the chromosomes can help. Elimination of other possible diseases by laboratory tests or x-rays will help determine the diagnosis.
Patients with familial Mediterranean fever may have any of the following during an attack:
- Elevated white blood cell count
- Elevated erythrocyte sedimentation rate (ESR)
- Elevated plasma fibrinogen
- Elevated serum haptoglobin
- Elevated ceruloplasmin
- Elevated C-reactive protein
Treatment
The treatment for familial Mediterranean fever is treatment of symptoms. Colchicine, a medicine that reduces inflammation, may help during an attack and may prevent further attacks.
Written and revised by
Andrey Nailor, M.D.
Our doctors write and review articles for accuracy and keep them up to date.
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