A Case of Protein Losing Enteropathy as Only Clinical manifestation of Systemic Lupus Erythematosus
Author(s) -
Tae Hyun Kim,
Yu Hee Choi,
Lae Hyung Kang,
Hyeong Jin Kim,
Jin Ho Jang,
Min Wook So
Publication year - 2017
Publication title -
kosin medical journal
Language(s) - English
Resource type - Journals
eISSN - 2586-7024
pISSN - 2005-9531
DOI - 10.7180/kmj.2017.32.1.84
Subject(s) - medicine , enteropathy , anti nuclear antibody , protein losing enteropathy , gastroenterology , edema , abdominal distension , systemic lupus , abdominal pain , dermatology , antibody , immunology , autoantibody , disease
Protein losing enteropathy (PLE) due to systemic lupus erythematosus (SLE) is relatively uncommon. PLE may be appeared sequentially after the diagnosis of SLE or concurrently with SLE. In most of concurrent cases, PLE was diagnosed one of various symptoms of SLE. Cases of PLE as the initial and only clinical presentation of SLE have been rarely reported. We described a 30-year old woman with general edema and abdominal distension was diagnosed PLE after stool alpha 1 antitrypsin clearance test. Her symptoms were getting worse even though the treatment with intravenous albumin. She was finally diagnosed PLE associated with SLE by additional laboratory findings (positive antinuclear antibody and anti-dsDNA IgG and low C3, C4 and CH50). She was treated with high dose of steroids and her symptoms were improved.
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