{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,15]],"date-time":"2026-10-15T22:14:39Z","timestamp":1792102479695,"version":"4.4.0"},"reference-count":18,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2023,11,29]],"date-time":"2023-11-29T00:00:00Z","timestamp":1701216000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Lupus"],"published-print":{"date-parts":[[2024,1]]},"abstract":"<jats:p>Lymphoid interstitial pneumonia (LIP) is a rare form of interstitial pulmonary disease, which has been described in association with a wide range of autoimmune disorders. Although the association of this entity with Sjogren\u2019s syndrome is well known, only a few cases are reported in relation to systemic lupus erythematosus (SLE). The aim of this paper is to review the cases reported in literature to date, as well as to describe the characteristics of these patients including the new case presented herein. We will be focusing on the case of a 36-year-old female patient diagnosed with SLE on hydroxychloroquine treatment who develops pleuritic chest pain and progressive dyspnea after 3\u00a0years of follow-up. The chest CT scan showed pleural thickening and both multiple and bilateral micronodules. A lung biopsy was also performed, revealing an infiltration of lymphocytes, plasma cells, and histiocytes in the alveolar septa suggestive of LIP. After conducting a review of the literature, we identified seven other cases describing SLE in association with LIP. The majority of them were young women, and LIP tends to appear early in the course of the disease, even as a form of initial presentation in some cases. Symptoms included cough, dyspnea, and pleuritic pain, with the exception of one case which was asymptomatic. It is noteworthy that half of the patients were positive for anti-SSA\/anti-SSB autoantibodies, and some of them also met criteria for Sjogren\u2019s syndrome. Treatment with steroids and other immunosuppressive agents improved symptoms in all of them.<\/jats:p>","DOI":"10.1177\/09612033231218957","type":"journal-article","created":{"date-parts":[[2023,11,29]],"date-time":"2023-11-29T07:51:36Z","timestamp":1701244296000},"page":"83-87","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":4,"title":["Lymphoid interstitial pneumonia in a patient with systemic lupus erythematosus: Case report and literature review"],"prefix":"10.1177","volume":"33","author":[{"ORCID":"https:\/\/orcid.org\/0009-0004-3870-3163","authenticated-orcid":false,"given":"Laura","family":"Dans Vil\u00e1n","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, Hospital Cl\u00ednico San Carlos, Madrid, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Raquel","family":"R\u00edos Fern\u00e1ndez","sequence":"additional","affiliation":[{"name":"Systemic Autoimmune 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Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Francisco Javier","family":"De la Hera","sequence":"additional","affiliation":[{"name":"Systemic Autoimmune Diseases Unit, Hospital Cl\u00ednico San Cecilio, Granada, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Norberto","family":"Ortego Centeno","sequence":"additional","affiliation":[{"name":"Department of Medicine, University of Granada, Granada, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jose Luis","family":"Callejas Rubio","sequence":"additional","affiliation":[{"name":"Systemic Autoimmune Diseases Unit, Hospital Cl\u00ednico San Cecilio, Granada, 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