Light chain proximal tubulopathy

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Amyloid proximal tubulopathy: a novel form of light chain proximal tubulopathy

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A 66-year-old retired librarian was referred to the nephrology clinic for evaluation of a recent onset of asymptomatic proteinuria identified at a routine hypertension check-up. She had a 15-year history of hypertension and was treated with ramipril and bendrofluomethazide with no history of diabetes. The urinary protein–creatinine ratio was elevated at 819 mg/mmol, with no evidence of glycosur...

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Light chain tubulopathy without Fanconi syndrome.

A 59-year-old white male was found to have mild proteinuria and renal insufficiency during a life insurance test in 2003. His serum creatinine has been stable at 1.6mg/dl since then. His 24 h urine protein was 720mg in 2003 and 861mg in 2006. Urinalysis showed 1þ protein with inactive sediment. His ANA, hepatitis B surface antigen, hepatitis C antibody and serum cryoglobulin were all negative. ...

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Light chain proximal tubulopathy (LCPT) is characterized by cytoplasmic inclusions of monoclonal LC within proximal tubular cells. The significance of crystalline versus noncrystalline LCPT and the effect of modern therapies are unknown. We reported the clinical-pathologic features of 40 crystalline and six noncrystalline LCPT patients diagnosed between 2000 and 2014. All crystalline LCPTs were...

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ژورنال

عنوان ژورنال: Kidney International

سال: 2009

ISSN: 0085-2538

DOI: 10.1038/ki.2008.666