Calcium oxalate and other crystals associated with kidney diseases and arthritis
Identifieur interne : 001A68 ( Istex/Corpus ); précédent : 001A67; suivant : 001A69Calcium oxalate and other crystals associated with kidney diseases and arthritis
Auteurs : Antonio J. Reginato ; Brenda KurnikSource :
- Seminars in Arthritis and Rheumatism [ 0049-0172 ] ; 1989.
English descriptors
- Teeft :
- Acute arthritis, Acute synovitis, Aluminum phosphate, American rheumatism association, Anhydrous cholesterol, Arch intern, Arch pathol, Arthritis, Arthritis immunology center, Arthritis rheum, Arthritis section, Arthropathy, Articular, Articular cartilage, Articular oxalosis, Articular tissues, Ascorbic, Ascorbic acid, Birefringent, Birefringent crystals, Blood vessels, Bone erosions, Bone marrow, Bone oxalosis, Bone pain, Bowel, Bowel disease, Bowel resection, Calcium, Calcium oxalate, Calcium oxalate crystals, Calcium oxalate monohydrate, Calcium oxalate nephrolithiasis, Calcium pyrophosphate dihydrate, Case report, Cell membranes, Charcotleyden crystals, Cholesterol crystals, Cholesterol emboli, Cholesterol tophus, Chronic dialysis, Chronic synovitis, Clin, Clin orthop, Clinical manifestations, Cottonlike calcific deposits, Cryoglobulin crystals, Crystal, Crystal deposition, Crystal formation, Crystalline deposits, Crystalline lipid, Crystallographic studies, Cystine, Cystine crystals, Cystinosis, Deposit, Deposition, Diffraction analysis, Disease states, Effusion, Engl, Enteric hyperoxaluria, Eosinophilic, Eosinophilic crystals, Eosinophilic synovitis, Familial hyperoxaluria, Fatty acids, Giant cells, Glyoxylate, Glyoxylate metabolism, Gout, Hematoidin crystals, Hemodialysis, Hemodialysis oxalosis, Hemodialysis patients, Hemodialyzed patients, Hemoglobin crystals, Higher values, Human eosinophil lysophospholipase, Hypereosinophilic syndrome, Hyperoxaluria, Hypoxanthine, Immunoglobulin, Inflammation, Intense birefringence, Intern, Intracellular, Intracellular crystals, Johns hopkins, Kidney, Kidney stones, Kurnik, Large amounts, Lglyceric acid, Light chains, Lipid, Lipid crystals, Lipid deposition, Lipids lipid, Liquid crystals, Manifestations articulaires, Metabolic basis, Metabolism, Microscopic studies, Microspherules, Mononuclear cells, Monosodium urate, More polymorphic, Multiple myeloma, Muscle pain, Musculoskeletal, Musculoskeletal manifestations, Myeloma, Myoglobin crystals, Negative birefringence, Nephrolithiasis, Nephropathic cystinosis, Nephrotic syndrome, Nonsteroidal antiinflammatory agents, Normal controls, Ordinary light, Original magnification, Other crystal, Other crystals, Other tissues, Oxalate, Oxalate crystals, Oxalate deposition, Oxalate metabolism, Oxalosis, Paraprotein, Paraprotein crystals, Pathological fractures, Peritoneal dialysis, Plasma cells, Platelike, Platelike crystals, Pleural effusion, Polyarthritis, Polymorphic crystals, Polymorphonuclear cells, Positive birefringency, Primary hyperoxaluria, Primary oxalosis, Primary oxaluria, Pyrophosphate, Reginato, Renal, Renal disease, Renal excretion, Renal failure, Renal osteodystrophy, Renal tissue, Rheum, Rheumatoid, Rheumatoid arthritis, Rheumatol, Rosettelike arrangement, Scanning electron microscopy, Schumacher, Secondary oxalosis, Serum oxalate, Sizes range, Skeletal muscle, Skin lesions, Stone formation, Such crystals, Syndrome, Synovial, Synovial cells, Synovial fluid, Synovial fluid oxalate levels, Synovitis, Synovium, Tissue deposits, Transmission electron microscopy, Tubular cells, Tubular lumen, Tubule, Ultrastructural study, Urate, Urinary, Urine, Watts, Xanthine, Xanthinuria.
Abstract
Abstract: The recognition of tissue deposits of crystalline material in a variety of organs, including the kidney, predated the association of crystals and arthritic disease. Because of this, the pathophysiology of crystal formation and its resultant inflammation is based in part on studies of renal stones. A number of disease states involving renal and articular crystallization exist. The most common of these, uric acid precipitation, or gout, and calcium phosphate precipitation were not reviewed in this discussion. This review described a variety of less common disease states involving articular and renal crystal deposition. The renal diseases discussed included both parenchymal or ectopic crystal deposition, as seen in nephrocalcinosis or cystinosis, and ductal crystallization as seen in renal calculus disease. The crystals involved included not only calcium oxalate, but also aluminum, amino acids and proteins (cystine, hemoglobin, cryoglobulins, and immunoglobulins), purine metabolites (xanthine, hypoxanthine), and even lipids and their degradative enzymes (cholesterol, phospholipids, phospholipase, and fatty acids). The simultaneous occurrence of crystals in both kidneys and joints was found in some cases to result from the systemic deposition of an excess of a particular biological compound. However, of more interest, some renal deposits were shown to more selectively reflect the normal or abnormal function of the kidney in its secretory and excretory roles. This is particularly evident in the variety of arthritic states described in end-stage renal disease.
Url:
DOI: 10.1016/0049-0172(89)90062-0
Links to Exploration step
ISTEX:567CDC41E33112D34F4BFCB1085F2E7EECD11E48Le document en format XML
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Reginato</name><affiliation><mods:affiliation>Arthritis Section, Cooper Hospital/University Medical Center USA</mods:affiliation></affiliation></author><author><name sortKey="Kurnik, Brenda" sort="Kurnik, Brenda" uniqKey="Kurnik B" first="Brenda" last="Kurnik">Brenda Kurnik</name><affiliation><mods:affiliation>UMDNJ/Robert Wood Johnson Medical School USA</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:567CDC41E33112D34F4BFCB1085F2E7EECD11E48</idno><date when="1989" year="1989">1989</date><idno type="doi">10.1016/0049-0172(89)90062-0</idno><idno type="url">https://api.istex.fr/ark:/67375/6H6-WX9BDP9K-B/fulltext.pdf</idno><idno type="wicri:Area/Istex/Corpus">001A68</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001A68</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a">Calcium oxalate and other crystals associated with kidney diseases and arthritis</title><author><name sortKey="Reginato, Antonio J" sort="Reginato, Antonio J" uniqKey="Reginato A" first="Antonio J." last="Reginato">Antonio J. Reginato</name><affiliation><mods:affiliation>Arthritis Section, Cooper Hospital/University Medical Center USA</mods:affiliation></affiliation></author><author><name sortKey="Kurnik, Brenda" sort="Kurnik, Brenda" uniqKey="Kurnik B" first="Brenda" last="Kurnik">Brenda Kurnik</name><affiliation><mods:affiliation>UMDNJ/Robert Wood Johnson Medical School USA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Seminars in Arthritis and Rheumatism</title><title level="j" type="abbrev">YSARH</title><idno type="ISSN">0049-0172</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1989">1989</date><biblScope unit="volume">18</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="198">198</biblScope><biblScope unit="page" to="224">224</biblScope></imprint><idno type="ISSN">0049-0172</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0049-0172</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acute arthritis</term><term>Acute synovitis</term><term>Aluminum phosphate</term><term>American rheumatism association</term><term>Anhydrous cholesterol</term><term>Arch intern</term><term>Arch pathol</term><term>Arthritis</term><term>Arthritis immunology center</term><term>Arthritis rheum</term><term>Arthritis section</term><term>Arthropathy</term><term>Articular</term><term>Articular cartilage</term><term>Articular oxalosis</term><term>Articular tissues</term><term>Ascorbic</term><term>Ascorbic acid</term><term>Birefringent</term><term>Birefringent crystals</term><term>Blood vessels</term><term>Bone erosions</term><term>Bone marrow</term><term>Bone oxalosis</term><term>Bone pain</term><term>Bowel</term><term>Bowel disease</term><term>Bowel resection</term><term>Calcium</term><term>Calcium oxalate</term><term>Calcium oxalate crystals</term><term>Calcium oxalate monohydrate</term><term>Calcium oxalate nephrolithiasis</term><term>Calcium pyrophosphate dihydrate</term><term>Case report</term><term>Cell membranes</term><term>Charcotleyden crystals</term><term>Cholesterol crystals</term><term>Cholesterol emboli</term><term>Cholesterol tophus</term><term>Chronic dialysis</term><term>Chronic synovitis</term><term>Clin</term><term>Clin orthop</term><term>Clinical manifestations</term><term>Cottonlike calcific deposits</term><term>Cryoglobulin crystals</term><term>Crystal</term><term>Crystal deposition</term><term>Crystal formation</term><term>Crystalline deposits</term><term>Crystalline lipid</term><term>Crystallographic studies</term><term>Cystine</term><term>Cystine crystals</term><term>Cystinosis</term><term>Deposit</term><term>Deposition</term><term>Diffraction analysis</term><term>Disease states</term><term>Effusion</term><term>Engl</term><term>Enteric hyperoxaluria</term><term>Eosinophilic</term><term>Eosinophilic crystals</term><term>Eosinophilic synovitis</term><term>Familial hyperoxaluria</term><term>Fatty acids</term><term>Giant cells</term><term>Glyoxylate</term><term>Glyoxylate metabolism</term><term>Gout</term><term>Hematoidin crystals</term><term>Hemodialysis</term><term>Hemodialysis oxalosis</term><term>Hemodialysis patients</term><term>Hemodialyzed patients</term><term>Hemoglobin crystals</term><term>Higher values</term><term>Human eosinophil lysophospholipase</term><term>Hypereosinophilic syndrome</term><term>Hyperoxaluria</term><term>Hypoxanthine</term><term>Immunoglobulin</term><term>Inflammation</term><term>Intense birefringence</term><term>Intern</term><term>Intracellular</term><term>Intracellular crystals</term><term>Johns hopkins</term><term>Kidney</term><term>Kidney stones</term><term>Kurnik</term><term>Large amounts</term><term>Lglyceric acid</term><term>Light chains</term><term>Lipid</term><term>Lipid crystals</term><term>Lipid deposition</term><term>Lipids lipid</term><term>Liquid crystals</term><term>Manifestations articulaires</term><term>Metabolic basis</term><term>Metabolism</term><term>Microscopic studies</term><term>Microspherules</term><term>Mononuclear cells</term><term>Monosodium urate</term><term>More polymorphic</term><term>Multiple myeloma</term><term>Muscle pain</term><term>Musculoskeletal</term><term>Musculoskeletal manifestations</term><term>Myeloma</term><term>Myoglobin crystals</term><term>Negative birefringence</term><term>Nephrolithiasis</term><term>Nephropathic cystinosis</term><term>Nephrotic syndrome</term><term>Nonsteroidal antiinflammatory agents</term><term>Normal controls</term><term>Ordinary light</term><term>Original magnification</term><term>Other crystal</term><term>Other crystals</term><term>Other tissues</term><term>Oxalate</term><term>Oxalate crystals</term><term>Oxalate deposition</term><term>Oxalate metabolism</term><term>Oxalosis</term><term>Paraprotein</term><term>Paraprotein crystals</term><term>Pathological fractures</term><term>Peritoneal dialysis</term><term>Plasma cells</term><term>Platelike</term><term>Platelike crystals</term><term>Pleural effusion</term><term>Polyarthritis</term><term>Polymorphic crystals</term><term>Polymorphonuclear cells</term><term>Positive birefringency</term><term>Primary hyperoxaluria</term><term>Primary oxalosis</term><term>Primary oxaluria</term><term>Pyrophosphate</term><term>Reginato</term><term>Renal</term><term>Renal disease</term><term>Renal excretion</term><term>Renal failure</term><term>Renal osteodystrophy</term><term>Renal tissue</term><term>Rheum</term><term>Rheumatoid</term><term>Rheumatoid arthritis</term><term>Rheumatol</term><term>Rosettelike arrangement</term><term>Scanning electron microscopy</term><term>Schumacher</term><term>Secondary oxalosis</term><term>Serum oxalate</term><term>Sizes range</term><term>Skeletal muscle</term><term>Skin lesions</term><term>Stone formation</term><term>Such crystals</term><term>Syndrome</term><term>Synovial</term><term>Synovial cells</term><term>Synovial fluid</term><term>Synovial fluid oxalate levels</term><term>Synovitis</term><term>Synovium</term><term>Tissue deposits</term><term>Transmission electron microscopy</term><term>Tubular cells</term><term>Tubular lumen</term><term>Tubule</term><term>Ultrastructural study</term><term>Urate</term><term>Urinary</term><term>Urine</term><term>Watts</term><term>Xanthine</term><term>Xanthinuria</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: The recognition of tissue deposits of crystalline material in a variety of organs, including the kidney, predated the association of crystals and arthritic disease. Because of this, the pathophysiology of crystal formation and its resultant inflammation is based in part on studies of renal stones. A number of disease states involving renal and articular crystallization exist. The most common of these, uric acid precipitation, or gout, and calcium phosphate precipitation were not reviewed in this discussion. This review described a variety of less common disease states involving articular and renal crystal deposition. The renal diseases discussed included both parenchymal or ectopic crystal deposition, as seen in nephrocalcinosis or cystinosis, and ductal crystallization as seen in renal calculus disease. The crystals involved included not only calcium oxalate, but also aluminum, amino acids and proteins (cystine, hemoglobin, cryoglobulins, and immunoglobulins), purine metabolites (xanthine, hypoxanthine), and even lipids and their degradative enzymes (cholesterol, phospholipids, phospholipase, and fatty acids). The simultaneous occurrence of crystals in both kidneys and joints was found in some cases to result from the systemic deposition of an excess of a particular biological compound. However, of more interest, some renal deposits were shown to more selectively reflect the normal or abnormal function of the kidney in its secretory and excretory roles. This is particularly evident in the variety of arthritic states described in end-stage renal disease.</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>synovial</json:string><json:string>oxalosis</json:string><json:string>lipid</json:string><json:string>oxalate</json:string><json:string>renal</json:string><json:string>synovial fluid</json:string><json:string>cholesterol crystals</json:string><json:string>birefringent</json:string><json:string>reginato</json:string><json:string>articular</json:string><json:string>hyperoxaluria</json:string><json:string>hemodialysis</json:string><json:string>rheumatoid</json:string><json:string>microspherules</json:string><json:string>clin</json:string><json:string>cystine</json:string><json:string>arthritis rheum</json:string><json:string>original 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stones</json:string><json:string>oxalate deposition</json:string><json:string>metabolic basis</json:string><json:string>skeletal muscle</json:string><json:string>renal excretion</json:string><json:string>secondary oxalosis</json:string><json:string>crystal formation</json:string><json:string>scanning electron microscopy</json:string><json:string>ordinary light</json:string><json:string>articular cartilage</json:string><json:string>urine</json:string><json:string>syndrome</json:string><json:string>pyrophosphate</json:string><json:string>gout</json:string><json:string>musculoskeletal manifestations</json:string><json:string>renal tissue</json:string><json:string>american rheumatism association</json:string><json:string>bowel disease</json:string><json:string>renal osteodystrophy</json:string><json:string>calcium oxalate monohydrate</json:string><json:string>articular oxalosis</json:string><json:string>negative birefringence</json:string><json:string>arch intern</json:string><json:string>sizes range</json:string><json:string>bone erosions</json:string><json:string>pathological fractures</json:string><json:string>large amounts</json:string><json:string>polymorphonuclear cells</json:string><json:string>paraprotein crystals</json:string><json:string>light chains</json:string><json:string>bowel resection</json:string><json:string>case report</json:string><json:string>calcium pyrophosphate dihydrate</json:string><json:string>hemoglobin crystals</json:string><json:string>other tissues</json:string><json:string>hemodialysis oxalosis</json:string><json:string>giant cells</json:string><json:string>bone marrow</json:string><json:string>blood vessels</json:string><json:string>calcium</json:string><json:string>metabolism</json:string><json:string>kidney</json:string><json:string>intern</json:string><json:string>deposit</json:string><json:string>intense birefringence</json:string><json:string>lipids lipid</json:string><json:string>nephrotic syndrome</json:string><json:string>liquid crystals</json:string><json:string>synovial fluid oxalate levels</json:string><json:string>mononuclear cells</json:string><json:string>intracellular crystals</json:string><json:string>eosinophilic synovitis</json:string><json:string>chronic synovitis</json:string><json:string>platelike crystals</json:string><json:string>anhydrous cholesterol</json:string><json:string>eosinophilic crystals</json:string><json:string>hypereosinophilic syndrome</json:string><json:string>tubular cells</json:string><json:string>tubular lumen</json:string><json:string>skin lesions</json:string><json:string>bone pain</json:string><json:string>cholesterol emboli</json:string><json:string>clinical manifestations</json:string><json:string>acute arthritis</json:string><json:string>cell membranes</json:string><json:string>cottonlike calcific deposits</json:string><json:string>cholesterol tophus</json:string><json:string>crystalline lipid</json:string><json:string>fatty acids</json:string><json:string>enteric hyperoxaluria</json:string><json:string>peritoneal dialysis</json:string><json:string>plasma cells</json:string><json:string>serum oxalate</json:string><json:string>rosettelike arrangement</json:string><json:string>chronic dialysis</json:string><json:string>stone formation</json:string><json:string>crystallographic studies</json:string><json:string>calcium oxalate nephrolithiasis</json:string><json:string>cryoglobulin crystals</json:string><json:string>clin orthop</json:string><json:string>higher values</json:string><json:string>more polymorphic</json:string><json:string>synovial cells</json:string><json:string>nephropathic cystinosis</json:string><json:string>diffraction analysis</json:string><json:string>positive birefringency</json:string><json:string>muscle pain</json:string><json:string>crystal deposition</json:string><json:string>polymorphic crystals</json:string><json:string>hemodialyzed patients</json:string><json:string>aluminum phosphate</json:string><json:string>lglyceric acid</json:string><json:string>myoglobin crystals</json:string><json:string>hematoidin crystals</json:string><json:string>disease states</json:string><json:string>glyoxylate metabolism</json:string><json:string>familial hyperoxaluria</json:string><json:string>manifestations articulaires</json:string><json:string>oxalate metabolism</json:string><json:string>normal controls</json:string><json:string>acute synovitis</json:string><json:string>nonsteroidal antiinflammatory agents</json:string><json:string>such crystals</json:string><json:string>arthritis immunology center</json:string><json:string>arthritis section</json:string><json:string>monosodium urate</json:string><json:string>primary oxaluria</json:string><json:string>birefringent crystals</json:string><json:string>arch pathol</json:string><json:string>johns hopkins</json:string><json:string>hemodialysis patients</json:string><json:string>lipid crystals</json:string><json:string>lipid deposition</json:string><json:string>ultrastructural study</json:string><json:string>other crystals</json:string><json:string>charcotleyden crystals</json:string><json:string>human eosinophil lysophospholipase</json:string><json:string>pleural effusion</json:string><json:string>microscopic studies</json:string><json:string>urinary</json:string></teeft></keywords><author><json:item><name>Antonio J. Reginato MD</name><affiliations><json:string>Arthritis Section, Cooper Hospital/University Medical Center USA</json:string></affiliations></json:item><json:item><name>Brenda Kurnik MD</name><affiliations><json:string>UMDNJ/Robert Wood Johnson Medical School USA</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Calcium oxalate</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>lipid crystals</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>arthritis</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>cholesterol crystals</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>cryoglobulins</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>kidney stones</value></json:item></subject><arkIstex>ark:/67375/6H6-WX9BDP9K-B</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Abstract: The recognition of tissue deposits of crystalline material in a variety of organs, including the kidney, predated the association of crystals and arthritic disease. Because of this, the pathophysiology of crystal formation and its resultant inflammation is based in part on studies of renal stones. A number of disease states involving renal and articular crystallization exist. The most common of these, uric acid precipitation, or gout, and calcium phosphate precipitation were not reviewed in this discussion. This review described a variety of less common disease states involving articular and renal crystal deposition. The renal diseases discussed included both parenchymal or ectopic crystal deposition, as seen in nephrocalcinosis or cystinosis, and ductal crystallization as seen in renal calculus disease. The crystals involved included not only calcium oxalate, but also aluminum, amino acids and proteins (cystine, hemoglobin, cryoglobulins, and immunoglobulins), purine metabolites (xanthine, hypoxanthine), and even lipids and their degradative enzymes (cholesterol, phospholipids, phospholipase, and fatty acids). The simultaneous occurrence of crystals in both kidneys and joints was found in some cases to result from the systemic deposition of an excess of a particular biological compound. However, of more interest, some renal deposits were shown to more selectively reflect the normal or abnormal function of the kidney in its secretory and excretory roles. This is particularly evident in the variety of arthritic states described in end-stage renal disease.</abstract><qualityIndicators><score>9.724</score><pdfWordCount>9279</pdfWordCount><pdfCharCount>70277</pdfCharCount><pdfVersion>1.4</pdfVersion><pdfPageCount>27</pdfPageCount><pdfPageSize>540 x 756 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>227</abstractWordCount><abstractCharCount>1590</abstractCharCount><keywordCount>6</keywordCount></qualityIndicators><title>Calcium oxalate and other crystals associated with kidney diseases and arthritis</title><pmid><json:string>2648579</json:string></pmid><pii><json:string>0049-0172(89)90062-0</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Proc Natl Acad Sci USA</title><language><json:string>unknown</json:string></language><volume>77</volume><pages><first>7440</first><last>7443</last></pages></serie><host><title>Seminars in Arthritis and Rheumatism</title><language><json:string>unknown</json:string></language><publicationDate>1989</publicationDate><issn><json:string>0049-0172</json:string></issn><pii><json:string>S0049-0172(00)X0072-8</json:string></pii><volume>18</volume><issue>3</issue><pages><first>198</first><last>224</last></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>1900s</json:string><json:string>1989</json:string><json:string>1900</json:string></date><geogName></geogName><orgName><json:string>American Rheumatism Association</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Dorothy A. Barnes</json:string><json:string>Al Characteristic</json:string><json:string>Brenda Kurnik</json:string><json:string>In</json:string><json:string>The</json:string><json:string>J.L. Ferreiro</json:string><json:string>Carolyn</json:string></persName><placeName></placeName><ref_url></ref_url><ref_bibl><json:string>Hoffman et al</json:string><json:string>Bland et al</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/6H6-WX9BDP9K-B</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - rheumatology</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - clinical medicine</json:string><json:string>3 - arthritis & rheumatology</json:string></scienceMetrix><scopus><json:string>1 - Health Sciences</json:string><json:string>2 - Medicine</json:string><json:string>3 - Anesthesiology and Pain Medicine</json:string><json:string>1 - Health Sciences</json:string><json:string>2 - Medicine</json:string><json:string>3 - Rheumatology</json:string></scopus><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string><json:string>2 - sciences biologiques et medicales</json:string><json:string>3 - sciences medicales</json:string></inist></categories><publicationDate>1989</publicationDate><copyrightDate>1989</copyrightDate><doi><json:string>10.1016/0049-0172(89)90062-0</json:string></doi><id>567CDC41E33112D34F4BFCB1085F2E7EECD11E48</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-WX9BDP9K-B/fulltext.pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-WX9BDP9K-B/bundle.zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/ark:/67375/6H6-WX9BDP9K-B/fulltext.tei"><teiHeader><fileDesc><titleStmt><title level="a">Calcium oxalate and other crystals associated with kidney diseases and arthritis</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher scheme="https://scientific-publisher.data.istex.fr">ELSEVIER</publisher><availability><licence><p>elsevier</p></licence></availability><p scheme="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M"></p><date>1989</date></publicationStmt><notesStmt><note type="research-article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</note><note type="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a">Calcium oxalate and other crystals associated with kidney diseases and arthritis</title><author xml:id="author-0000"><persName><forename type="first">Antonio J.</forename><surname>Reginato</surname></persName><roleName type="degree">MD</roleName><note type="biography">Chief, Professor of Medicine, Clinical Associate Professor of Medicine, Attending Consultant</note><note type="biography">Address reprint requests to Antonio J. Reginato, MD, Division of Rheumatology, Cooper Hospital/University Medical Center, 3 Cooper Plaza, Camden, NJ 08103.</note><affiliation>Chief, Professor of Medicine, Clinical Associate Professor of Medicine, Attending Consultant</affiliation><affiliation>Address reprint requests to Antonio J. Reginato, MD, Division of Rheumatology, Cooper Hospital/University Medical Center, 3 Cooper Plaza, Camden, NJ 08103.</affiliation><affiliation>Arthritis Section, Cooper Hospital/University Medical Center USA</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Brenda</forename><surname>Kurnik</surname></persName><roleName type="degree">MD</roleName><note type="biography">Attending Physician, Assistant Professor of Medicine</note><note type="biography">From the Arthritis Section and Division of Nephrology, Cooper Hospital/University Medical Center, Camden, NJ.</note><affiliation>Attending Physician, Assistant Professor of Medicine</affiliation><affiliation>From the Arthritis Section and Division of Nephrology, Cooper Hospital/University Medical Center, Camden, NJ.</affiliation><affiliation>UMDNJ/Robert Wood Johnson Medical School USA</affiliation></author><idno type="istex">567CDC41E33112D34F4BFCB1085F2E7EECD11E48</idno><idno type="ark">ark:/67375/6H6-WX9BDP9K-B</idno><idno type="DOI">10.1016/0049-0172(89)90062-0</idno><idno type="PII">0049-0172(89)90062-0</idno></analytic><monogr><title level="j">Seminars in Arthritis and Rheumatism</title><title level="j" type="abbrev">YSARH</title><idno type="pISSN">0049-0172</idno><idno type="PII">S0049-0172(00)X0072-8</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1989"></date><biblScope unit="volume">18</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="198">198</biblScope><biblScope unit="page" to="224">224</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1989</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Abstract: The recognition of tissue deposits of crystalline material in a variety of organs, including the kidney, predated the association of crystals and arthritic disease. Because of this, the pathophysiology of crystal formation and its resultant inflammation is based in part on studies of renal stones. A number of disease states involving renal and articular crystallization exist. The most common of these, uric acid precipitation, or gout, and calcium phosphate precipitation were not reviewed in this discussion. This review described a variety of less common disease states involving articular and renal crystal deposition. The renal diseases discussed included both parenchymal or ectopic crystal deposition, as seen in nephrocalcinosis or cystinosis, and ductal crystallization as seen in renal calculus disease. The crystals involved included not only calcium oxalate, but also aluminum, amino acids and proteins (cystine, hemoglobin, cryoglobulins, and immunoglobulins), purine metabolites (xanthine, hypoxanthine), and even lipids and their degradative enzymes (cholesterol, phospholipids, phospholipase, and fatty acids). The simultaneous occurrence of crystals in both kidneys and joints was found in some cases to result from the systemic deposition of an excess of a particular biological compound. However, of more interest, some renal deposits were shown to more selectively reflect the normal or abnormal function of the kidney in its secretory and excretory roles. This is particularly evident in the variety of arthritic states described in end-stage renal disease.</p></abstract><textClass><keywords scheme="keyword"><list><head>Keywords</head><item><term>Calcium oxalate</term></item><item><term>lipid crystals</term></item><item><term>arthritis</term></item><item><term>cholesterol crystals</term></item><item><term>cryoglobulins</term></item><item><term>kidney stones</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1989">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-WX9BDP9K-B/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla"><item-info><jid>YSARH</jid><aid>89900620</aid><ce:pii>0049-0172(89)90062-0</ce:pii><ce:doi>10.1016/0049-0172(89)90062-0</ce:doi><ce:copyright type="unknown" year="1989"></ce:copyright></item-info><head><ce:title>Calcium oxalate and other crystals associated with kidney diseases and arthritis</ce:title><ce:author-group><ce:author><ce:given-name>Antonio J.</ce:given-name><ce:surname>Reginato</ce:surname><ce:degrees>MD</ce:degrees><ce:roles>Chief, Professor of Medicine, Clinical Associate Professor of Medicine, Attending Consultant</ce:roles><ce:cross-ref refid="COR1"><ce:sup>∗</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Brenda</ce:given-name><ce:surname>Kurnik</ce:surname><ce:degrees>MD</ce:degrees><ce:roles>Attending Physician, Assistant Professor of Medicine</ce:roles><ce:cross-ref refid="FN2"><ce:sup>2</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF2"><ce:sup>2</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF3"><ce:sup>3</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF4"><ce:sup>4</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF5"><ce:sup>e</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF6"><ce:sup>f</ce:sup></ce:cross-ref><ce:cross-ref refid="FN1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:affiliation id="AFF1"><ce:label>a</ce:label><ce:textfn>Arthritis Section, Cooper Hospital/University Medical Center USA</ce:textfn></ce:affiliation><ce:affiliation id="AFF2"><ce:label>b</ce:label><ce:textfn>UMDNJ/Robert Wood Johnson Medical School USA</ce:textfn></ce:affiliation><ce:affiliation id="AFF3"><ce:label>c</ce:label><ce:textfn>University of Pennsylvania USA</ce:textfn></ce:affiliation><ce:affiliation id="AFF4"><ce:label>d</ce:label><ce:textfn>Arthritis Immunology Center, Philadelphia Veterans' Administration Medical Center USA</ce:textfn></ce:affiliation><ce:affiliation id="AFF5"><ce:label>e</ce:label><ce:textfn>Division of Nephrology, Cooper Hospital/University Medical Center USA</ce:textfn></ce:affiliation><ce:affiliation id="AFF6"><ce:label>f</ce:label><ce:textfn>UMDNJ/Robert Wood Johnson Medical Center USA</ce:textfn></ce:affiliation><ce:correspondence id="COR1"><ce:label>∗</ce:label><ce:text>Address reprint requests to Antonio J. Reginato, MD, Division of Rheumatology, Cooper Hospital/University Medical Center, 3 Cooper Plaza, Camden, NJ 08103.</ce:text></ce:correspondence><ce:footnote id="FN1"><ce:label>1</ce:label><ce:note-para>From the Arthritis Section and Division of Nephrology, Cooper Hospital/University Medical Center, Camden, NJ.</ce:note-para></ce:footnote><ce:footnote id="FN2"><ce:label>2</ce:label><ce:note-para>From the Department of Medicine, UMDNJ/Robert Wood Johnson, Medical Center, Camden, NJ.</ce:note-para></ce:footnote></ce:author-group><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para>The recognition of tissue deposits of crystalline material in a variety of organs, including the kidney, predated the association of crystals and arthritic disease. Because of this, the pathophysiology of crystal formation and its resultant inflammation is based in part on studies of renal stones. A number of disease states involving renal and articular crystallization exist. The most common of these, uric acid precipitation, or gout, and calcium phosphate precipitation were not reviewed in this discussion. This review described a variety of less common disease states involving articular and renal crystal deposition. The renal diseases discussed included both parenchymal or ectopic crystal deposition, as seen in nephrocalcinosis or cystinosis, and ductal crystallization as seen in renal calculus disease. The crystals involved included not only calcium oxalate, but also aluminum, amino acids and proteins (cystine, hemoglobin, cryoglobulins, and immunoglobulins), purine metabolites (xanthine, hypoxanthine), and even lipids and their degradative enzymes (cholesterol, phospholipids, phospholipase, and fatty acids). The simultaneous occurrence of crystals in both kidneys and joints was found in some cases to result from the systemic deposition of an excess of a particular biological compound. However, of more interest, some renal deposits were shown to more selectively reflect the normal or abnormal function of the kidney in its secretory and excretory roles. This is particularly evident in the variety of arthritic states described in end-stage renal disease.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:keywords class="idt"><ce:section-title>Keywords</ce:section-title><ce:keyword><ce:text>Calcium oxalate</ce:text></ce:keyword><ce:keyword><ce:text>lipid crystals</ce:text></ce:keyword><ce:keyword><ce:text>arthritis</ce:text></ce:keyword><ce:keyword><ce:text>cholesterol crystals</ce:text></ce:keyword><ce:keyword><ce:text>cryoglobulins</ce:text></ce:keyword><ce:keyword><ce:text>kidney stones</ce:text></ce:keyword></ce:keywords></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Calcium oxalate and other crystals associated with kidney diseases and arthritis</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Calcium oxalate and other crystals associated with kidney diseases and arthritis</title></titleInfo><name type="personal"><namePart type="given">Antonio J.</namePart><namePart type="family">Reginato</namePart><namePart type="termsOfAddress">MD</namePart><description>Chief, Professor of Medicine, Clinical Associate Professor of Medicine, Attending Consultant</description><affiliation>Arthritis Section, Cooper Hospital/University Medical Center USA</affiliation><description>Address reprint requests to Antonio J. Reginato, MD, Division of Rheumatology, Cooper Hospital/University Medical Center, 3 Cooper Plaza, Camden, NJ 08103.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Brenda</namePart><namePart type="family">Kurnik</namePart><namePart type="termsOfAddress">MD</namePart><description>Attending Physician, Assistant Professor of Medicine</description><affiliation>UMDNJ/Robert Wood Johnson Medical School USA</affiliation><description>From the Arthritis Section and Division of Nephrology, Cooper Hospital/University Medical Center, Camden, NJ.</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1989</dateIssued><copyrightDate encoding="w3cdtf">1989</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: The recognition of tissue deposits of crystalline material in a variety of organs, including the kidney, predated the association of crystals and arthritic disease. Because of this, the pathophysiology of crystal formation and its resultant inflammation is based in part on studies of renal stones. A number of disease states involving renal and articular crystallization exist. The most common of these, uric acid precipitation, or gout, and calcium phosphate precipitation were not reviewed in this discussion. This review described a variety of less common disease states involving articular and renal crystal deposition. The renal diseases discussed included both parenchymal or ectopic crystal deposition, as seen in nephrocalcinosis or cystinosis, and ductal crystallization as seen in renal calculus disease. The crystals involved included not only calcium oxalate, but also aluminum, amino acids and proteins (cystine, hemoglobin, cryoglobulins, and immunoglobulins), purine metabolites (xanthine, hypoxanthine), and even lipids and their degradative enzymes (cholesterol, phospholipids, phospholipase, and fatty acids). The simultaneous occurrence of crystals in both kidneys and joints was found in some cases to result from the systemic deposition of an excess of a particular biological compound. However, of more interest, some renal deposits were shown to more selectively reflect the normal or abnormal function of the kidney in its secretory and excretory roles. This is particularly evident in the variety of arthritic states described in end-stage renal disease.</abstract><subject><genre>Keywords</genre><topic>Calcium oxalate</topic><topic>lipid crystals</topic><topic>arthritis</topic><topic>cholesterol crystals</topic><topic>cryoglobulins</topic><topic>kidney stones</topic></subject><relatedItem type="host"><titleInfo><title>Seminars in Arthritis and Rheumatism</title></titleInfo><titleInfo type="abbreviated"><title>YSARH</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1989</dateIssued></originInfo><identifier type="ISSN">0049-0172</identifier><identifier type="PII">S0049-0172(00)X0072-8</identifier><part><date>1989</date><detail type="volume"><number>18</number><caption>vol.</caption></detail><detail type="issue"><number>3</number><caption>no.</caption></detail><extent unit="issue-pages"><start>151</start><end>224</end></extent><extent unit="pages"><start>198</start><end>224</end></extent></part></relatedItem><identifier type="istex">567CDC41E33112D34F4BFCB1085F2E7EECD11E48</identifier><identifier type="ark">ark:/67375/6H6-WX9BDP9K-B</identifier><identifier type="DOI">10.1016/0049-0172(89)90062-0</identifier><identifier type="PII">0049-0172(89)90062-0</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-WX9BDP9K-B/record.json</uri></json:item></metadata></istex></record>Pour manipuler ce document sous Unix (Dilib)
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