Related Experiment Video
Updated: Nov 12, 2025

Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
Celiac Disease as a Rare Cause of Membranous Nephropathy: A Case Report
Nicole Pestana1, Carlota Vida1, Pedro Vieira1
1Nephrology Department, Hospital Central do Funchal, Funchal, PRT.
Insights
Membranous nephropathy, a kidney disorder, can be linked to celiac disease. This case highlights a patient with celiac disease who developed membranous nephropathy, emphasizing the need for early diagnosis and tailored treatment strategies.
Area of Science:
- Nephrology
- Gastroenterology
- Immunology
Background:
- Membranous nephropathy is a leading cause of nephrotic syndrome in adults.
- Systemic conditions are associated with a significant number of membranous nephropathy cases.
- Celiac disease is an autoimmune disorder triggered by gluten consumption.
Abstract:
Membranous nephropathy is the most common cause of nephrotic syndrome in adults. A non-negligible number of cases are associated with systemic conditions. We report a case of a 50-year-old man who presented with nephrotic syndrome six months after being diagnosed with celiac disease. Although the patient showed disappearance of circulating immunoglobulin A (IgA) anti-tissue transglutaminase antibodies following a gluten-free diet, he had a sudden onset of nephrotic syndrome presenting with severe hypoalbuminemia. Other secondary causes were promptly excluded leading to the assumption of celiac disease-associated membranous nephropathy with remission after treatment with angiotensin system blockade and a gluten-free diet. The goal of this case report is to alert the clinic towards this rare association aiming for an early diagnosis and adequate selection of long-term therapy.
More Related Videos
Related Concept Videos
Nephrotic Syndrome I : Introduction
Nephrotic Syndrome II : Assessment and Medical Management
Chronic Kidney Disease II: Clinical Manifestations
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Nephrons

