Orphanet Journal of Rare Diseases | 2021

Clinical features of lupus enteritis: a single-center retrospective study

 
 
 
 
 
 
 
 

Abstract


Background Lupus enteritis (LEn) is a rare complication of systemic lupus erythematosus (SLE). Timely diagnosis and treatment of LEn are necessary to prevent the most serious consequences — intestinal perforation, gastrointestinal bleeding, and death. We compared the clinical features of SLE patients with and without LEn. Methods The clinical data of LEn inpatients at Suining Central Hospital from July 2012 to June 2020 were examined. These LEn patients were matched (1:2 ratio) with concurrently hospitalized SLE patients who did not have LEn. The two groups were compared using multivariate logistic regression. Results We compared SLE inpatients with LEn (n\u2009=\u200943) and SLE inpatients without LEn (n\u2009=\u200986) at our institution. Multivariate logistic regression showed that ascites (odds ratio [OR]: 9.961, 95%CI: 2.215–44.802, P \u2009=\u20090.003), hydronephrosis (OR: 28.060, 95%CI: 2.303–341.962, P \u2009=\u20090.009), leukopenia (OR: 5.890, 95%CI: 1.813–19.135, P \u2009=\u20090.003), reduced complement C3 level (OR: 4.791, 95%CI: 1.605–14.300, P \u2009=\u20090.005), and elevated immunoglobin (Ig)A level (OR: 4.040, 95%CI: 1.307–12.487, P \u2009=\u20090.015) were independently associated with LEn. Within the LEn group, abdominal pain was the most common abdominal symptom (88.4%), and increased mesenteric fat attenuation (74.4%) and bowel wall thickening (58.1%) were the most common computed tomography (CT) findings. Most LEn patients (88.4%) required high-dose glucocorticoid therapy (≥\u200980\xa0mg methylprednisolone/day), and cyclophosphamide was the most commonly used immunosuppressant (62.8%). Conclusions Abdominal pain was the most common clinical symptom of LEn. Abdominal CT provides important information for detection and diagnosis of LEn. Ascites, hydronephrosis, leukopenia, hypocomplementemia (C3), and increased IgA were independently associated with LEn.

Volume 16
Pages None
DOI 10.1186/s13023-021-02044-4
Language English
Journal Orphanet Journal of Rare Diseases

Full Text