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BMC Nephrol ; 22(1): 277, 2021 08 10.
Artículo en Inglés | MEDLINE | ID: mdl-34376183

RESUMEN

BACKGROUND: Horseshoe kidney (HSK) is a common congenital defect of the urinary system. The most common complications are urinary tract infection, urinary stones, and hydronephrosis. HSK can be combined with glomerular diseases, but the diagnosis rate of renal biopsy is low due to structural abnormalities. There are only a few reports on HSK with glomerular disease. Here, we have reported a case of PLA2R-positive membranous nephropathy occurring in a patient with HSK. CASE PRESENTATION: After admission to the hospital due to oedema of both the lower extremities, the patient was diagnosed with nephrotic syndrome due to abnormal 24-h urine protein (7540 mg) and blood albumin (25 g/L) levels. Abdominal ultrasonography revealed HSK. The patient's brother had a history of end-stage renal disease due to nephrotic syndrome. Therefore, the patient was diagnosed with PLA2R-positive stage II membranous nephropathy through renal biopsy under abdominal ultrasonography guidance. He was administered adequate prednisone and cyclophosphamide, and after 6 months of treatment, urinary protein excretion levels significantly decreased. CONCLUSION: The risk and difficulty of renal biopsy in patients with HSK are increased due to structural abnormalities; however, renal biopsy can be accomplished through precise positioning with abdominal ultrasonography. In the literature, 20 cases of HSK with glomerular disease have been reported thus far. Because of the small number of cases, estimating the incidence rate of glomerular diseases in HSK is impossible, and the correlation between HSK and renal pathology cannot be stated. Further studies should be conducted and cases should be accumulated to elucidate this phenomenon.


Asunto(s)
Edema , Riñón Fusionado , Glomerulonefritis Membranosa , Biopsia Guiada por Imagen/métodos , Riñón , Síndrome Nefrótico , Proteinuria , Diagnóstico Diferencial , Edema/diagnóstico , Edema/etiología , Riñón Fusionado/complicaciones , Riñón Fusionado/diagnóstico por imagen , Riñón Fusionado/genética , Riñón Fusionado/patología , Glomerulonefritis Membranosa/diagnóstico , Glomerulonefritis Membranosa/etiología , Glomerulonefritis Membranosa/fisiopatología , Humanos , Riñón/diagnóstico por imagen , Riñón/patología , Extremidad Inferior , Masculino , Persona de Mediana Edad , Síndrome Nefrótico/diagnóstico , Síndrome Nefrótico/etiología , Síndrome Nefrótico/fisiopatología , Atención al Paciente/métodos , Proteinuria/diagnóstico , Proteinuria/etiología , Receptores de Fosfolipasa A2 , Resultado del Tratamiento , Ultrasonografía/métodos
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