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Upper endoscopy and colonoscopy showed normal duodenal and colonic mucosae. Both infectious and malignancy workup were also unremarkable. Bereft of other systemic symptoms, autoimmune pathology was initially deemed unlikely; however, autoimmune workup revealed positive antinuclear antibody, double-stranded DNA, anti-Smith antibody, antinuclear ribonucleoprotein and hypocomplementaemia. With multidisciplinary collaboration, the patient was initiated on high-dose steroids, which dramatically improved her symptoms. She was discharged home with a steroid taper, and at 3 months of follow-up with her rheumatologist, she was continued on steroids and hydroxychloroquine.<\/jats:p>","DOI":"10.1136\/bcr-2020-239072","type":"journal-article","created":{"date-parts":[[2021,8,24]],"date-time":"2021-08-24T12:38:06Z","timestamp":1629808686000},"page":"e239072","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":2,"title":["Lupus enteritis as a lone manifestation of SLE: rare but possible"],"prefix":"10.1136","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6253-5065","authenticated-orcid":false,"given":"Eduardo","family":"Quintero","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, Albert Einstein Medical Center, Philadelphia, Pennsylvania, 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