Extractions: Vol. 140 No. 3, March 1, 1980 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Hulter HN Bonner EL Articles that cite this article Contact me when this article is cited H. N. Hulter and E. L. Bonner Jr Acute oliguric renal failure previously was reported to develop in patients with preexisting idiopathic nephrotic syndrome in association with clinical evidence of vascular volume depletion. We describe an 81-year-old man without recent proteinuria or evidence of preexisting nephrotic syndrome in whom acute oliguric renal failure developed. Renal biopsy disclosed minimal change disease. Nephrotic range proteinuria without severe hypoalbuminemia
Extractions: This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Alert me to new issues of the journal Add to My File Cabinet ... Download to citation manager PubMed Articles by Block, W. M. Articles by Butsch, M. P. Pediatrics, Jun 1948, 733-753, Vol 1, No. 6 WM Block, RL Jackson, G Stearns and MP Butsch Department of Pediatrics, College of Medicine, State University of Iowa. Our purpose is to present experiences gained from the study of children with nephrosis observed in the Children's Hospital of the State University of Iowa during the past 15 years. The diagnosis of nephrosis was made only when the following criteria were met: presence of edema, proteinuria, good renal concentration ability, high blood fats and low blood protein with marked decrease in the albumin fraction; absence of retinopathy, persistent
Lipoid Nephrosis lipoid nephrosis. Nephrotic syndrome. Electron micrograph. Previous Next 1 2 3 4 5 Return to Systemic Pathology Page. http://biomed.brown.edu/Courses/BI279/Lec09/Lec09-D.htm
Lipoid Nephrosis » Medical Diagnosis lipoid nephrosis. Medical Diagnosis » L » lipoid nephrosis 581.3 lipoidnephrosis (see images) Want to discuss this term? http://www.medfamily.org/diagnosis/L/diagnosis-terms-Lipoid_nephrosis.phtml
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Karger Publishers Cytokine mRNA Profile in lipoid nephrosis Evidence for Increased IL8 mRNAStability Paul F. Laflam, Soichi Haraguchi, Eduardo H. Garin http://content.karger.com/ProdukteDB/produkte.asp?Doi=65022
Minimal Change Disease(lipoid Nephrosis) Minimal change disease(lipoid nephrosis) Minimal change disease(lipoid nephrosis).Histologically normalappearing glomeruli are seen in a renal biopsy http://ajoupath.ajou.ac.kr/slides/kd6.htm
Extractions: This Article correspondence: Submit a response Alert me when this article is cited Alert me when correspondence are posted Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Gur, A. Articles by Hayslett, J. P. A Gur, PY Adefuin, NJ Siegel and JP Hayslett Children with lipoid nephrosis were studies during clinical relapse and after complete remission. As expected, the calculated serum oncotic pressure was reduced severely from the remission value of 28.6 +/- 0.9 mm Hg to 15.4 +/- 1.1 (P less than 0.005) during relapse. Although no apparent change in plasma volume was noted using the volume of distribution of labeled human albumin, calculated plasma volume was reduced 13 +/- 8% during relapse when estimated from changes in hematocrit. After a water
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EMedicine - Nephrotic Syndrome : Article By Luther Travis, MD Synonyms and related keywords NS, nephrosis, lipoid nephrosis, Briefly, thename was modified to lipoid nephrosis after the routine finding of lipid http://www.emedicine.com/PED/topic1564.htm
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Nephrology Last Updated: April 14, 2005 Rate this Article Email to a Colleague Synonyms and related keywords: NS, nephrosis, lipoid nephrosis, primary nephrotic syndrome, primary NS, PNS, idiopathic nephrotic syndrome, idiopathic NS, INS, secondary nephrotic syndrome, secondary NS, minimal change nephrotic syndrome, MCNS, minimal lesion nephrotic syndrome, MLNS, nil disease, steroid-sensitive nephrotic syndrome, SSNS, steroid-resistant nephrotic syndrome, SRNS, steroid-dependent nephrotic syndrome, SDNS, mesangial proliferative glomerulonephritis, MPN, immunoglobulin M nephropathy, focal segmental glomerulosclerosis, FSGS, membranoproliferative or mesangiocapillary glomerulonephritis, MPGN, hypocomplementemic glomerulonephritis, membranous glomerulonephritis, MGN, congenital nephrotic syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Extractions: (advertisement) Synonyms, Key Words, and Related Terms: NS, nephrosis, lipoid nephrosis, primary nephrotic syndrome, primary NS, PNS, idiopathic nephrotic syndrome, idiopathic NS, INS, secondary nephrotic syndrome, secondary NS, minimal change nephrotic syndrome, MCNS, minimal lesion nephrotic syndrome, MLNS, nil disease, steroid-sensitive nephrotic syndrome, SSNS, steroid-resistant nephrotic syndrome, SRNS, steroid-dependent nephrotic syndrome, SDNS, mesangial proliferative glomerulonephritis, MPN, immunoglobulin M nephropathy, focal segmental glomerulosclerosis, FSGS, membranoproliferative or mesangiocapillary glomerulonephritis, MPGN, hypocomplementemic glomerulonephritis, membranous glomerulonephritis, MGN, congenital nephrotic syndrome Background: The term nephrosis, or nephrotic syndrome, had its origin in the early 20th century and was introduced primarily to distinguish it from nephritis, a label used to denote a clinical state associated with hematuria, proteinuria, and a cellular proliferation of the glomerulus. It describes a clinical condition of edema and proteinuria in which the renal histology (light microscopy) demonstrates fatty degeneration of the tubules associated with normal appearing glomeruli. Briefly, the name was modified to lipoid nephrosis after the routine finding of lipid droplets in the urine of affected patients. The subcategories of PNS are based on histologic descriptions, but clinical-pathological correlations have been made. Even though knowledge of specific causes of NS are too limited for more precise classification, the variants of PNS/INS will be considered as clinical disease states with well-defined histopathologic processes. The histologic type at onset makes it possible to generalize about such things as response to therapy and ultimate prognosis. When possible, the authors use the definitions, descriptions, and nomenclature developed by the International Study of Kidney Diseases in Children (ISKDC). Most attention will be devoted to minimal change nephrotic syndrome (MCNS) and focal segmental glomerulosclerosis (FSGS) with only modest attention to familial or congenital nephrosis, membranoproliferative glomerulonephritis (MPGN), and membranous glomerulonephritis (MGN).
Kidneys - Nephrotic Syndrome Minimal change (lipoid nephrosis) this type is most common in children, Minimal Change disease (lipoid nephrosis) is the most common form of http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Kidneys_nephrotic
Minimal Change Disease Alternative Names. Minimal change nephrotic syndrome; Nil disease; lipoid nephrosis;Idiopathic nephrotic syndrome of childhood http://www.ehendrick.org/healthy/000496.htm
Extractions: Injury Disease Nutrition Poison ... Prevention Minimal change disease is a kidney disorder. Each kidney is made of more than a million units called nephrons. Each nephron has a tuft of blood vessels called a glomerulus, which is surrounded by a Bowman's Capsule. Together, these structures filter blood and form urine. Minimal change disease is one cause of nephrotic syndrome . It is named "minimal change" because the nephrons appear totally normal under a light microscope. The condition is only seen using an electron microscope, which reveals changes in the Bowman's Capsule in the nephrons. Urine tests also show high protein levels. Minimal change nephrotic syndrome; Nil disease; Lipoid nephrosis; Idiopathic nephrotic syndrome of childhood Minimal change disease is the most common cause of nephrotic syndrome in children. It is also frequently seen in adults. The cause is unknown, but the disease may be preceded by viral infection, allergic reactions, or recent immunizations. Minimal change disease does not reduce the amount of urine produced. It rarely progresses to
JN 2003; Vol.16 N°1: 148-153 One patient had focal glomerulosclerosis and lipoid nephrosis. lipoid nephrosisand focal glomerulosclerosis in a patient with polymyositis. http://www.sin-italy.org/jnonline/vol16n1/148.html
Extractions: Table of Contents Case report J NEPHROL 2003; 16: 148-153 Unexpected IgA nephropathy during the treatment of a young woman with idiopathic dermatomyositis: Case report and review of the literature Tzung-Hai Yen , Jeng-Yi Huang , Chen-Yin Chen Department of Nephrology, Department of Pediatrics, Chang Gung Memorial Hospital, Taipei, Taiwan - China ABSTRACT: This article reports the unexpected discovery of IgA nephropathy in a 26-year-old Chinese woman 1.5 years after the onset of idiopathic dermatomyositis. The patient was taking immunosuppressive agents, prednisolone 25 mg and azathioprine 75 mg daily. Glomerulonephritis associated with idiopathic polymyositis/dermatomyositis is rare. A review of the medical literature indicates that the most common pattern seen in idiopathic polymyositis is mesangial proliferative glomerulonephritis. However, both membranous and mesangial proliferative glomerulonephritis are often seen in idiopathic dermatomyositis. It is still not clear, however, whether the humorally- mediated immune process in dermatomyositis and the cell-mediated immune process in polymyositis can explain the different patterns of occurrence of glomerular lesions in these two closely related disease entities. Key words: Dermatomyositis, Polymyositis, Nephrotic syndrome, IgA nephropathy
REFERENCES Pathogenesis of lipoid nephrosis a disorder of Tcell function. Lancet 1974;2 (7880) 556-60. 47.Candiano G, Musante L, Zennaro C, Bruschi M, Carraro M, http://www.sin-italy.org/jnonline/forum/fsgs/references.htm
Penn State Faculty Research Expertise Database (FRED) , Glomerular disease causing heavy proteinuria Lipoid Nephroses, lipoid nephrosis. Minimal Change GlomerulonephritidesNephrosis, Lipoid. http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D009402
