A simultaneous occurrence of Tolosa-Hunt syndrome and fibrillary glomerulonephritis: a case report
Autor: | Rossella Cianci, Roberta Renzulli, Antonietta Gigante, Konstantinos Giannakakis, Francesca Borghesi, Marcella Visentini, Massimo Fiorilli, Biagio Barbano |
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Jazyk: | angličtina |
Rok vydání: | 2009 |
Předmět: |
medicine.medical_specialty
medicine.medical_treatment Biopsy Kidney Glomerulus Renal function Mild proteinuria Gastroenterology Pathology and Forensic Medicine Glomerulonephritis Internal medicine Tolosa-Hunt Syndrome medicine Humans Dialysis Diplopia Proteinuria medicine.diagnostic_test business.industry Fibrillary Glomerulonephritis General Medicine Middle Aged medicine.disease Surgery Female Renal biopsy medicine.symptom business Tolosa–Hunt syndrome |
Popis: | Fibrillary glomerulonephritis (FibGN) is a rare cause of progressive renal dysfunction, often leading to dialysis within a few years. A 60-year-old woman presented with a 2 month history of right-sided retro-orbital pain and recent diplopia. Laboratory testing revealed an altered renal function with increased serum creatinine and mild proteinuria. MRI of the brain revealed the presence of a soft tissue mass on the right cavernous sinus compatible with the diagnosis of Tolosa–Hunt syndrome (THS). Renal biopsy showed a pattern compatible with fibrillary glomerulonephritis. For this reason steroid therapy was initiated at a dose of 1 mg/kg/day and adjusted according to the clinical course. Neurological symptoms regressed shortly after the beginning of therapy and renal function and proteinuria remained stable for the 3 years following the withdrawal of steroid therapy. Percutaneous renal biopsy was again performed and confirmed the previous diagnosis of FibGN in association with other glomerular-lesion-like mesangial widening, thickening of capillary walls and severe arterio-arteriolosclerosis. This case report describes what is believed to first report of the association of FibGN and THS, which both responded to steroid therapy. |
Databáze: | OpenAIRE |
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