Osteomalacia revealing Sjögren's syndrome: a case report
The most common renal disease in Sjögren's syndrome is tubulo-interstitial nephritis, responsible for tubular acidosis in around 20 % of patients. Osteomalacia exceptionally occurs as the first manifestation of a renal tubule disorder due to a Sjögren's syndrome. We report a case of a 20-y...
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Veröffentlicht in: | La revue de medecine interne 2008-04, Vol.29 (4), p.311-314 |
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creator | Jallouli, M Frigui, M Marzouk, S Kaddour, N Kechaou, M Frikha, F Bahloul, Z |
description | The most common renal disease in Sjögren's syndrome is tubulo-interstitial nephritis, responsible for tubular acidosis in around 20 % of patients. Osteomalacia exceptionally occurs as the first manifestation of a renal tubule disorder due to a Sjögren's syndrome.
We report a case of a 20-year-old woman with tubular acidosis induced osteomalacia secondary to primary Sjögren's syndrome. Improvement was obtained with bicarbonates, vitamin D, calcium and high-dose steroid therapy.
During Sjögren's syndrome, osteomalacia can complicate the distal renal tubular acidosis. In spite of the rare cases of osteomalacia revealing Sjögren's syndrome, this auto-immune disease must appear in the list of the aetiologies of osteomalacia. |
doi_str_mv | 10.1016/j.revmed.2007.09.028 |
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We report a case of a 20-year-old woman with tubular acidosis induced osteomalacia secondary to primary Sjögren's syndrome. Improvement was obtained with bicarbonates, vitamin D, calcium and high-dose steroid therapy.
During Sjögren's syndrome, osteomalacia can complicate the distal renal tubular acidosis. In spite of the rare cases of osteomalacia revealing Sjögren's syndrome, this auto-immune disease must appear in the list of the aetiologies of osteomalacia.</description><identifier>ISSN: 0248-8663</identifier><identifier>DOI: 10.1016/j.revmed.2007.09.028</identifier><identifier>PMID: 18023938</identifier><language>fre</language><publisher>France</publisher><subject>Acidosis, Renal Tubular - etiology ; Adult ; Female ; Humans ; Mobility Limitation ; Osteomalacia - etiology ; Sjogren's Syndrome - diagnosis</subject><ispartof>La revue de medecine interne, 2008-04, Vol.29 (4), p.311-314</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18023938$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jallouli, M</creatorcontrib><creatorcontrib>Frigui, M</creatorcontrib><creatorcontrib>Marzouk, S</creatorcontrib><creatorcontrib>Kaddour, N</creatorcontrib><creatorcontrib>Kechaou, M</creatorcontrib><creatorcontrib>Frikha, F</creatorcontrib><creatorcontrib>Bahloul, Z</creatorcontrib><title>Osteomalacia revealing Sjögren's syndrome: a case report</title><title>La revue de medecine interne</title><addtitle>Rev Med Interne</addtitle><description>The most common renal disease in Sjögren's syndrome is tubulo-interstitial nephritis, responsible for tubular acidosis in around 20 % of patients. Osteomalacia exceptionally occurs as the first manifestation of a renal tubule disorder due to a Sjögren's syndrome.
We report a case of a 20-year-old woman with tubular acidosis induced osteomalacia secondary to primary Sjögren's syndrome. Improvement was obtained with bicarbonates, vitamin D, calcium and high-dose steroid therapy.
During Sjögren's syndrome, osteomalacia can complicate the distal renal tubular acidosis. In spite of the rare cases of osteomalacia revealing Sjögren's syndrome, this auto-immune disease must appear in the list of the aetiologies of osteomalacia.</description><subject>Acidosis, Renal Tubular - etiology</subject><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Mobility Limitation</subject><subject>Osteomalacia - etiology</subject><subject>Sjogren's Syndrome - diagnosis</subject><issn>0248-8663</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kMtKxDAYhbNQnHH0DUS60lXrn6TNxZ0M3mBgFuq6pOmfoaU3k44wL-YL-GIGHFfnLD4-OIeQKwoZBSru2szjV491xgBkBjoDpk7IEliuUiUEX5DzEFoAiLQ-IwuqgHHN1ZLobZhx7E1nbGOSaEHTNcMueWt_vnceh9uQhMNQ-7HH-8Qk1gSM1DT6-YKcOtMFvDzminw8Pb6vX9LN9vl1_bBJJ8r1nDpHjRDCOmdNFatyjFLQNdMOmKxkrVReOWToBC8sE7kAwSR1Qspa5CD5itz8eSc_fu4xzGXfBItdZwYc96GUkBesoBDB6yO4r-IX5eSb3vhD-T-W_wKEcVZq</recordid><startdate>200804</startdate><enddate>200804</enddate><creator>Jallouli, M</creator><creator>Frigui, M</creator><creator>Marzouk, S</creator><creator>Kaddour, N</creator><creator>Kechaou, M</creator><creator>Frikha, F</creator><creator>Bahloul, Z</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200804</creationdate><title>Osteomalacia revealing Sjögren's syndrome: a case report</title><author>Jallouli, M ; Frigui, M ; Marzouk, S ; Kaddour, N ; Kechaou, M ; Frikha, F ; Bahloul, Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p139t-ff1a666cffcab1a68f21109d29f027b7d884bfe2ef635c264606271f677d64073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>fre</language><creationdate>2008</creationdate><topic>Acidosis, Renal Tubular - etiology</topic><topic>Adult</topic><topic>Female</topic><topic>Humans</topic><topic>Mobility Limitation</topic><topic>Osteomalacia - etiology</topic><topic>Sjogren's Syndrome - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jallouli, M</creatorcontrib><creatorcontrib>Frigui, M</creatorcontrib><creatorcontrib>Marzouk, S</creatorcontrib><creatorcontrib>Kaddour, N</creatorcontrib><creatorcontrib>Kechaou, M</creatorcontrib><creatorcontrib>Frikha, F</creatorcontrib><creatorcontrib>Bahloul, Z</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>La revue de medecine interne</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jallouli, M</au><au>Frigui, M</au><au>Marzouk, S</au><au>Kaddour, N</au><au>Kechaou, M</au><au>Frikha, F</au><au>Bahloul, Z</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteomalacia revealing Sjögren's syndrome: a case report</atitle><jtitle>La revue de medecine interne</jtitle><addtitle>Rev Med Interne</addtitle><date>2008-04</date><risdate>2008</risdate><volume>29</volume><issue>4</issue><spage>311</spage><epage>314</epage><pages>311-314</pages><issn>0248-8663</issn><abstract>The most common renal disease in Sjögren's syndrome is tubulo-interstitial nephritis, responsible for tubular acidosis in around 20 % of patients. Osteomalacia exceptionally occurs as the first manifestation of a renal tubule disorder due to a Sjögren's syndrome.
We report a case of a 20-year-old woman with tubular acidosis induced osteomalacia secondary to primary Sjögren's syndrome. Improvement was obtained with bicarbonates, vitamin D, calcium and high-dose steroid therapy.
During Sjögren's syndrome, osteomalacia can complicate the distal renal tubular acidosis. In spite of the rare cases of osteomalacia revealing Sjögren's syndrome, this auto-immune disease must appear in the list of the aetiologies of osteomalacia.</abstract><cop>France</cop><pmid>18023938</pmid><doi>10.1016/j.revmed.2007.09.028</doi><tpages>4</tpages></addata></record> |
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subjects | Acidosis, Renal Tubular - etiology Adult Female Humans Mobility Limitation Osteomalacia - etiology Sjogren's Syndrome - diagnosis |
title | Osteomalacia revealing Sjögren's syndrome: a case report |
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