Adhesive small-bowel obstruction as a challenging complication of familial Mediterranean fever: A case-based review
- PMID: 37575017
- DOI: 10.1111/1756-185X.14867
Adhesive small-bowel obstruction as a challenging complication of familial Mediterranean fever: A case-based review
Abstract
Familial Mediterranean fever (FMF) is the most common inherited autoinflammatory disorder, characterized by recurrent and self-limiting episodes of fever and serosal inflammation. Recurrent serositis may rarely lead to the formation of adhesions in the peritoneum, which may result in mechanical bowel obstruction. The symptoms, such as abdominal pain and vomiting, may mimic typical FMF attacks, resulting in misdiagnosis and severe morbidity, including strangulation and intestinal necrosis. Physicians are generally aware of other complications associated with FMF but reports on peritoneal adhesions and intestinal obstruction in English-language literature are inadequate to increase clinicians' awareness. Therefore, it is crucial to meticulously evaluate FMF patients presenting with abdominal pain and ileus because these symptoms could be due to adhesive small-bowel obstruction (ASBO). Furthermore, patients presenting with ASBO without a history of abdominal surgery should also be thoroughly evaluated, especially as it could be an initial presentation for an autoinflammatory disease. Herein, we present a pediatric case of FMF with the M694V homozygous mutation, complicated by ASBO while under colchicine treatment. Additionally, we provide a comprehensive review of the available literature on ASBO in FMF.
Keywords: adhesive small-bowel obstruction; familial Mediterranean fever; peritoneal adhesions.
© 2023 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.
References
REFERENCES
-
- Yalçinkaya F, Ozen S, Ozçakar ZB, et al. A new set of criteria for the diagnosis of familial Mediterranean fever in childhood. Rheumatology (Oxford). 2009;48(4):395-398. doi:10.1093/rheumatology/ken509
-
- Ben-Chetrit E, Touitou I. Familial mediterranean fever in the world. Arthritis Rheum. 2009;61(10):1447-1453. doi:10.1002/art.24458
-
- “Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever.” The International FMF Consortium. Cell. 1997;90(4):797-807. doi:10.1016/s0092-8674(00)80539-5
-
- Park YH, Wood G, Kastner DL, Chae JJ. Pyrin inflammasome activation and RhoA signaling in the autoinflammatory diseases FMF and HIDS. Nat Immunol. 2016;17(8):914-921. doi:10.1038/ni.3457
-
- Öztürk K, Coşkuner T, Baglan E, et al. Real-life data from the largest pediatric familial Mediterranean fever cohort. Front Pediatr. 2022;9:805919. doi:10.3389/fped.2021.805919
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
