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Lung cancer-associated membranous nephropathy with positive anti-PLA2R autoantibodies: a case report
Mouna Jerbi1, Mouna Riguen1,2, Asma Bettaieb1,2
1Laboratory of Kidney Pathology LR01SP01, University Tunis El Manar, Tunis, Tunisia.
Abstract:
Membranous nephropathy (MN) is a common cause of idiopathic nephrotic syndrome in adults. The identification of the phospholipase A2 receptor 1 (PLA2R) as a podocyte antigen in adult patients with MN allows clinicians to quickly and accurately diagnose primary MN. Secondary forms associated with malignancy, medications, infection, or autoimmune disease do not generally express anti-PLA2R autoantibodies. We describe a case of a 66-year-old woman who presented with impure nephrotic syndrome, and a renal biopsy showed MN. The diagnosis of secondary MN was initially retained despite positive Anti- PLA2R in light of the discovery of a pulmonary adenocarcinoma. However, nephrotic syndrome persisted after surgical treatment and tumor remission. Remission was only achieved after the use of immunosuppressive therapy. Our case teaches us that even in the presence of an evident etiology for MN, the diagnosis of primary form should always be reconsidered in the absence of remission, especially when anti-PLA2R antibodies are positive.
Insights
Membranous nephropathy (MN) diagnosis requires careful consideration. Even with a secondary cause like cancer, persistent nephrotic syndrome with positive anti-PLA2R antibodies may indicate a primary form requiring immunosuppression.
Area of Science:
- Nephrology
- Immunology
- Oncology
Background:
- Membranous nephropathy (MN) is a leading cause of nephrotic syndrome in adults.
- Phospholipase A2 receptor 1 (PLA2R) autoantibodies are key biomarkers for primary MN.
- Secondary MN can be linked to malignancy, infections, medications, or autoimmune diseases, typically lacking anti-PLA2R antibodies.
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