1. Antibrush Border Antibody Disease: A Case Report and Literature Review
- Author
-
Laíse Pereira Arcoverde Fechine Brito, Felipe Leite Guedes, Pedro Henrique Cavalcante Vale, Rivaldo Pereira Santos, José Bruno de Almeida, Sílvia Queiroz Santos Martins, Gleiko Yuri de Figueredo Dantas, David Wanderley, Stanley de Almeida Araújo, and Gyl Eanes Barros Silva
- Subjects
Anti-brush border antibody disease ,anti-LRP2 nephropathy ,auto-antibodies ,autoimmunity ,chronic kidney disease ,kidney biopsy ,Diseases of the genitourinary system. Urology ,RC870-923 - Abstract
Anti-brush border antibody (ABBA) disease, also called anti–low-density lipoprotein receptor-related protein 2 (anti-LRP2) nephropathy, occurs due to the formation of antibodies against brush border antigens of the renal proximal convoluted tubule. We report a case of ABBA disease in a male farmer in his 30s who presented with 2 years of polyuria, dysuria, nocturia, and urinary urgency. He described a history of long-term occupational exposure to pesticides and silica, evolving into possible pneumoconiosis, and prior pulmonary tuberculosis. At presentation, he had reduced kidney function (serum creatinine 3.6 mg/dL) with hyponatremia, hypokalemia, hypophosphatemia, a normal anion gap, metabolic acidosis, and respiratory acidosis, and 2.2 g/day of urine proteinuria. The kidney biopsy was consistent with ABBA, showing amorphous immune-deposits in the tubular basement membrane and strong positivity on indirect immunofluorescence in the brush border of the proximal tubules. The trigger for production of ABBA is still unknown, but it may be associated with chronic conditions such as pulmonary tuberculosis and occupational exposures such as silica and pesticides, as seen in the patient in this report. Most cases do not respond to immunosuppression, and the prognosis is poor.
- Published
- 2021
- Full Text
- View/download PDF