Abdominal syndrome in monogenic autoinflammatory disease – is it just a familial Mediterranean fever?
https://doi.org/10.14412/1996-7012-2020-4-144-149
Abstract
The paper describes a clinical case of the classic manifestations of TRAPS (fever, rash, periorbital edema, arthritis, and elevated levels of acutephase inflammatory markers) concurrent with severe abdominalgia during attacks and with the development of severe peritoneal adhesions, which led to bowel perforation and emergency surgical intervention. The prolonged persistence of inflammatory attacks before the initiation of therapy, as well as violation of the IL1 inhibitor administration regimen facilitated the development of an urgent exacerbation. Thus, TRAPS should be included in the differential diagnostic circle for patients with severe gastrointestinal manifestations characterized by an attack-like course. These patients need timely prescription of targeted therapy, strict adherence to the dosing and intervals between drug administrations, and careful monitoring to prevent serious complications with the visceral organs, including the gastrointestinal tract, and their immediate correction.
About the Authors
S. O. SaluginaRussian Federation
Laboratory of Pediatric Rheumatic Diseases
34A, Kashirskoe Shosse, Moscow 115522, Russia;
E. S. Fedorov
Russian Federation
Laboratory of Pediatric Rheumatic Diseases
34A, Kashirskoe Shosse, Moscow 115522, Russia;
N. G. Volf
Russian Federation
2A, Academician Kirensky St., Krasnoyarsk 660074, Russia
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Review
For citations:
Salugina SO, Fedorov ES, Volf NG. Abdominal syndrome in monogenic autoinflammatory disease – is it just a familial Mediterranean fever? Sovremennaya Revmatologiya=Modern Rheumatology Journal. 2020;14(4):144-149. (In Russ.) https://doi.org/10.14412/1996-7012-2020-4-144-149