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Pseudo–pseudo Meigs' syndrome (PPMS) in chronic lupus peritonitis: a case report with review of literature
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Citations
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References
2021
Year
VasculitisPseudo-pseudo MeigsImmunologyGastroenterologyPathologySignificant AscitesClinical FindingPseudo–pseudo MeigsAutoimmune DiseaseAllergySystemic Lupus ErythematosusSystemic Lupus Erythematosus TreatmentChronic Lupus PeritonitisSystemic SclerodermaLupus NephritisAutoimmunityImmunologic DiseaseSclerodermaCase ReportLupusMedicine
Gastrointestinal involvement in systemic lupus erythematosus (SLE) usually occurs in the form of mesenteric vasculitis, protein-losing enteropathy, intestinal pseudo-obstruction, and pancreatitis. We describe a 23-year-old female, a known case of SLE presented with significant ascites and pleural effusion. Further evaluation showed elevated CA-125 levels without evidence of malignancy. The patient was treated with corticosteroids, hydroxychloroquine, and azathioprine resulting in the resolution of ascites in 2 weeks. The triad of ascites, pleural effusion, and increased CA-125 is known as pseudo-pseudo Meigs' syndrome, which is rarely reported in the literature. Clinicians should be aware of this entity while evaluating an SLE patient with low serum-ascites albumin gradient (SAAG) ascites.
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