karyomegalic tubulointerstitial nephritis: a rare cause of chronic kidney disease

نویسندگان

ebru uz department of nephrology, fatih university medical school, turkey

yeter bayram department of internal medicine, fatih university medical school, turkey +90-03122035555, [email protected]; department of internal medicine, fatih university medical school, turkey +90-03122035555, [email protected]

hacer haltas department of nephrology, fatih university medical school, turkey

nuket bavbek department of nephrology, fatih university medical school, turkey

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Acute and Chronic Tubulointerstitial Nephritis

Cellular and fluid exudation in the interstitial tissue was noted by Councilman in 1898, while he studied kidneys of patients who died of scarlet fever and diphtheria (1). Councilman also determined that these kidneys did not contain bacteria (they were sterile). He called the condition acute interstitial nephritis (AIN). The term interstitial nephritis connotes predominant involvement of the r...

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Karyomegalic Interstitial Nephritis

Karyomegalic interstitial nephritis is a rare cause of hereditary chronic interstitial nephritis, described for the first time over 40 years ago.A 36-year-old woman, of Turkish origin, presented with chronic kidney disease and high blood pressure. She had a history of recurrent upper respiratory tract infections but no familial history of nephropathy. Physical examination was unremarkable. Labo...

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Explorer FAN 1 mutations cause karyomegalic interstitial nephritis , linking chronic kidney failure to defective DNA damage repair

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Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.

Apolipoprotein A-I amyloidosis is a rare, late-onset, autosomal dominant condition characterized by systemic deposition of amyloid in tissues, the major clinical problems being related to renal, hepatic, and cardiac involvement. Described is the clinical and histologic picture of renal involvement as a result of apolipoprotein A-I amyloidosis in five families of Italian ancestry. In all of the ...

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Progressive chronic kidney disease secondary to tubulointerstitial nephritis in primary biliary cirrhosis

Primary biliary cirrhosis (PBC) is an autoimmune disease characterized by the presence of anti-mitochondrial antibodies (AMA). Whilst asymptomatic distal tubular acidosis (DTA) is the commonest renal lesion reported in PBC, tubulointerstitial nephritis (TIN) has also been reported as a rare association. Although PBC could be a familial disorder, there have been no previous reports of familial c...

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PReS-FINAL-2266: A rare cause for childhood uveitis: TINU (tubulointerstitial nephritis and uveitis) syndrome

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عنوان ژورنال:
nephro-urology monthly

جلد ۳، شماره ۳، صفحات ۲۰۱-۲۰۳

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