Rare Diagnosis in a Patient with Diabetes with Nephrotic Proteinuria

Autor: Mário Góis, Patricia Cotovio, Ariana Azevedo, Fernando Nolasco
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Male
Nephrotic Syndrome
Nephrotic Syndrome / etiology
Biopsy
030232 urology & nephrology
Disease
030204 cardiovascular system & hematology
urologic and male genital diseases
Gastroenterology
Vascular Access Devices / standards
0302 clinical medicine
Glomerulonephritis
Nephrotic Syndrome / diagnosis
Proteinuria
medicine.diagnostic_test
Glucocorticoids / therapeutic use
HCC NEF
General Medicine
Amyloidosis
Middle Aged
Treatment Outcome
Prednisolone
Renal biopsy
medicine.symptom
Amyloidosis / diagnosis
Vascular Access Devices
medicine.drug
medicine.medical_specialty
Proteinuria / diagnosis
Renal function
Proteinuria / etiology
03 medical and health sciences
Glomerulonephritis / pathology
Rare Diseases
Rare Disease
Internal medicine
Diabetes mellitus
medicine
Humans
Diabetes Mellitus
Type 2 / complications

Prednisolone / therapeutic use
Glucocorticoids
Diabetes Mellitus
Type 2 / epidemiology

business.industry
Type 2 Diabetes Mellitus
medicine.disease
Diabetes Mellitus
Type 2

Biopsy / methods
Prednisolone / administration & dosage
Nephrotic Syndrome / pathology
business
Nephrotic syndrome
Zdroj: BMJ Case Rep
Popis: We report a 63-year-old man with well-controlled type 2 diabetes mellitus and hypertension, who presented with new onset nephrotic proteinuria and rapid deterioration in renal function. The atypical clinical presentation prompted us to consider a non-diabetic and non-hypertensive cause and to perform a renal biopsy. A diagnosis of fibrillarglomerulonephritis (FGn) was made based on electronic microscopy. Proteinuria remained in nephrotic range despite treatment with prednisolone, and renal function deteriorated. We suggest that other causes of proteinuria should be considered in patients with diabetes who present with the nephrotic syndrome when there is no other evidence of microvascular disease. We review the spectrum of fibrillar glomerulopathies including FGn, primary and secondary amyloidosis and immunotactoid glomerulonephritis. info:eu-repo/semantics/publishedVersion
Databáze: OpenAIRE