Bone Marrow Edema and Pseudocyst as a Very Rare Complication of Familial Mediterranean Fever: A Case Report
Journal Title: Bagcilar Medical Bulletin - Year 2018, Vol 3, Issue 3
Abstract
Familial Mediterranean fever (FMF) is one of the most common autoinflammatory diseases. FMF is a disease that characterized by recurrent fever, transient and self-limiting polyserositis, responds well to the treatment of colchicine. In 95% of patients, the first attack occurs with severe abdominal pain. The first attack frequency that starts with pleuritic chest pain, pleural effusion and fever are lower than 10%. Ninety percent of the cases are younger than 20 years old. After 40 years old, it is rarely diagnosed (1.25%). In this case report; we wanted to present an FMF case diagnosed after 40 years old in the context of the patient's clinical follow-up, treatment, and literature, since it is very rare to diagnose in this age group, and unexpected complications can occur.
Authors and Affiliations
Abuzer Coskun, Sevki Hakan Eren, Mehmet Eren, Sedat Ozbay
Keywords
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- EP ID EP50342
- DOI 10.5350/BMB20180718070737
- Views 209
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