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Familial Mediteranean fever with protein-losing enteropathy due to constrictive pericarditis 
 
Familial Mediteranean fever with protein-losing enteropathy due to constrictive pericarditis
  İbrahim Gökçe, Selim Gökçe, Ayhan Kılıç, Uğur Bozlar, Murat Kocaoğlu, Önder Öng¨¹r¨¹, Faysal Gök
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Ankara, Turkey

Author Affiliations: Department of Pediatric Nephrology and Rheumatology (Gökçe İ, Gök F), Department of Pediatric Gastroenterology (Gökçe S), Department of Pediatric Cardiology (Kılıç A), Department of Radiology (Bozlar U, Kocaoğlu M), and Department of Pathology (Öng¨¹r¨¹ Ö), G¨¹lhane Military Academy of Medicine, School of Medicine, 06018, Etlik, Ankara, Turkey

Corresponding Author: İbrahim Gökçe, Department of Pediatric Nephrology, G¨¹lhane Military Medical Academy, School of Medicine, 06018, Etlik, Ankara, Turkey (Tel:  0 (506) 7035001; Fax: 09 0312 304 43 81; Email: gokcemd@yahoo.com)

doi: 10.1007/s12519-011-0255-y

Background: Constrictive pericarditis (CP) represents a rare cause of protein-losing enteropathy (PLE) resulting from intestinal lymphangiectasia (IL). In this report, we describe an 8-year-old Turkish boy with IL and PLE secondary to CP.

Methods: The boy was introduced to our clinic due to bilateral pretibial edema and swelling of the eyelids caused by hypoproteinemia. Physical examination revealed a distended right jugular vein. Laboratory investigation revealed PLE with fecal concentration of alpha-1 antitripsin of 4.87 mg/g. Histopathologic examination of random biopsies obtained from the duodenum revealed markedly dilated lymphatics compatible with IL. Constrictive pericarditis was diagnosed by tagged cine cardiac magnetic resonance imaging.

Results: Pericardiectomy was performed for the patient. Genetic analysis was done and heterozygous mutation E148Q was detected as a disease-causing Mediterranean fever (MEFV) mutation. Colchicine was started after the operation. Six months after the initiation of regular colchicine therapy, echocardiography revealed disappearance of CP.

Conclusion: This is the first reported case of PLE with a distended right jugular vein due to CP secondary to familial Mediterranean fever associated with E148Q heterozygosity in the MEFV gene.

Key words: constrictive pericarditis; familial Mediterranean fever; intestinal lymphangiectasia; protein-losing enteropathy

World J Pediatr 2011;7(4):365-367

 
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