Familial Mediterranean fever presenting as recurrent acute pelvic inflammatory disease

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A Palestinian woman with recurrent pelvic pain refractory to antibiotics was successfully treated with colchicine, leading to a diagnosis of familial Mediterranean fever rather than endometriosis or infectious pelvic inflammatory disease.

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Abstract

BACKGROUND: Recurrent acute episodes of pelvic inflammatory disease (PID) often present a diagnostic dilemma. The differential diagnosis should include reinfection, appendicitis, endometriosis, irritable bowel syndrome, colitis, persistent ovarian cyst, and antibiotic-resistant bacterial strains. CASE: NA young Palestinian woman presented with recurrent episodes of pelvic pain with rebound tenderness, fever, and elevated white blood cell count, erythrocyte sedimentation rate, and C-reactive protein. The patient underwent extensive workup, multiple courses of intravenous and oral antibiotics, and diagnostic laparoscopies, with continued recurrent episodes. Treatment with colchicine for suspected familial Mediterranean fever resulted in resolution of symptoms. CONCLUSION: In patients of Mediterranean ancestry who have symptoms of recurrent PID that are refractory to conventional treatment, familial Mediterranean fever should be included in the differential diagnosis.

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Condition tags

endometriosisirritable_bowel_syndrome

MeSH descriptors

Familial Mediterranean Fever Pelvic Inflammatory Disease Adult Diagnosis, Differential Familial Mediterranean Fever Female Humans Pelvic Inflammatory Disease Recurrence

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europepmc
last seen: 2026-10-03T06:16:46.921020+00:00
pubmed
last seen: 2026-05-13T22:12:50.257867+00:00
unpaywall
last seen: 2026-10-03T06:31:36.481334+00:00
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