Sclerosing cholangitis and systemic lymphadenopathy
A 48-year-old man was admitted to our hospital with jaundice and systemic lymphadenopathy. Cholangiographic findings and liver histology disclosed the presence of sclerosing cholangitis. The patient also had a marked polyclonal increase in IgG levels. The cholangiographic findings, the systemic lymp...
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Veröffentlicht in: | Journal of gastroenterology 2001-06, Vol.36 (6), p.429-432 |
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container_title | Journal of gastroenterology |
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creator | Kazumori, H Hashimoto, T Akagi, S Adachi, K Watanabe, M Kinoshita, Y |
description | A 48-year-old man was admitted to our hospital with jaundice and systemic lymphadenopathy. Cholangiographic findings and liver histology disclosed the presence of sclerosing cholangitis. The patient also had a marked polyclonal increase in IgG levels. The cholangiographic findings, the systemic lymphadenopathy, and the increase in IgG levels resolved completely after treatment with prednisolone. This case suggests that there is an association between sclerosing cholangitis and immunologic abnormalities, and that corticosteroid treatment is useful for this disorder. |
doi_str_mv | 10.1007/s005350170089 |
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Cholangiographic findings and liver histology disclosed the presence of sclerosing cholangitis. The patient also had a marked polyclonal increase in IgG levels. The cholangiographic findings, the systemic lymphadenopathy, and the increase in IgG levels resolved completely after treatment with prednisolone. This case suggests that there is an association between sclerosing cholangitis and immunologic abnormalities, and that corticosteroid treatment is useful for this disorder.</description><identifier>ISSN: 0944-1174</identifier><identifier>EISSN: 1435-5922</identifier><identifier>DOI: 10.1007/s005350170089</identifier><identifier>PMID: 11428591</identifier><language>eng</language><publisher>Japan</publisher><subject>Cholangitis, Sclerosing - complications ; Humans ; Lymphatic Diseases - complications ; Lymphatic Diseases - immunology ; Male ; Middle Aged</subject><ispartof>Journal of gastroenterology, 2001-06, Vol.36 (6), p.429-432</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-57787bcf17c74290f860882a8e294eb6076957316c35a7958f2b633d213eee733</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11428591$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kazumori, H</creatorcontrib><creatorcontrib>Hashimoto, T</creatorcontrib><creatorcontrib>Akagi, S</creatorcontrib><creatorcontrib>Adachi, K</creatorcontrib><creatorcontrib>Watanabe, M</creatorcontrib><creatorcontrib>Kinoshita, Y</creatorcontrib><title>Sclerosing cholangitis and systemic lymphadenopathy</title><title>Journal of gastroenterology</title><addtitle>J Gastroenterol</addtitle><description>A 48-year-old man was admitted to our hospital with jaundice and systemic lymphadenopathy. Cholangiographic findings and liver histology disclosed the presence of sclerosing cholangitis. The patient also had a marked polyclonal increase in IgG levels. The cholangiographic findings, the systemic lymphadenopathy, and the increase in IgG levels resolved completely after treatment with prednisolone. This case suggests that there is an association between sclerosing cholangitis and immunologic abnormalities, and that corticosteroid treatment is useful for this disorder.</description><subject>Cholangitis, Sclerosing - complications</subject><subject>Humans</subject><subject>Lymphatic Diseases - complications</subject><subject>Lymphatic Diseases - immunology</subject><subject>Male</subject><subject>Middle Aged</subject><issn>0944-1174</issn><issn>1435-5922</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkDtPwzAUhS0EoqUwsqJMbIF7_YjtEVUUkCoxAHPkODdNUF7E6ZB_T6tGQkxn-XR0zsfYLcIDAujHAKCEAtQAxp6xJUqhYmU5P2dLsFLGiFou2FUI3wAoQJlLtkCU3CiLSyY-fE1DF6p2F_myq127q8YqRK7NozCFkZrKR_XU9KXLqe16N5bTNbsoXB3oZs4V-9o8f65f4-37y9v6aRt7IfkYK62NznyB2mvJLRQmAWO4M8StpCwBnVilBSZeKKetMgXPEiFyjoKItBArdn_q7YfuZ09hTJsqeKoPI6nbh1SDTbjEIxifQH94EgYq0n6oGjdMKUJ6tJT-s3Tg7-bifdZQ_kfPWsQvyCdgig</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Kazumori, H</creator><creator>Hashimoto, T</creator><creator>Akagi, S</creator><creator>Adachi, K</creator><creator>Watanabe, M</creator><creator>Kinoshita, Y</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>20010601</creationdate><title>Sclerosing cholangitis and systemic lymphadenopathy</title><author>Kazumori, H ; Hashimoto, T ; Akagi, S ; Adachi, K ; Watanabe, M ; Kinoshita, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-57787bcf17c74290f860882a8e294eb6076957316c35a7958f2b633d213eee733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Cholangitis, Sclerosing - complications</topic><topic>Humans</topic><topic>Lymphatic Diseases - complications</topic><topic>Lymphatic Diseases - immunology</topic><topic>Male</topic><topic>Middle Aged</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kazumori, H</creatorcontrib><creatorcontrib>Hashimoto, T</creatorcontrib><creatorcontrib>Akagi, S</creatorcontrib><creatorcontrib>Adachi, K</creatorcontrib><creatorcontrib>Watanabe, M</creatorcontrib><creatorcontrib>Kinoshita, Y</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazumori, H</au><au>Hashimoto, T</au><au>Akagi, S</au><au>Adachi, K</au><au>Watanabe, M</au><au>Kinoshita, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sclerosing cholangitis and systemic lymphadenopathy</atitle><jtitle>Journal of gastroenterology</jtitle><addtitle>J Gastroenterol</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>36</volume><issue>6</issue><spage>429</spage><epage>432</epage><pages>429-432</pages><issn>0944-1174</issn><eissn>1435-5922</eissn><abstract>A 48-year-old man was admitted to our hospital with jaundice and systemic lymphadenopathy. Cholangiographic findings and liver histology disclosed the presence of sclerosing cholangitis. The patient also had a marked polyclonal increase in IgG levels. The cholangiographic findings, the systemic lymphadenopathy, and the increase in IgG levels resolved completely after treatment with prednisolone. This case suggests that there is an association between sclerosing cholangitis and immunologic abnormalities, and that corticosteroid treatment is useful for this disorder.</abstract><cop>Japan</cop><pmid>11428591</pmid><doi>10.1007/s005350170089</doi><tpages>4</tpages></addata></record> |
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subjects | Cholangitis, Sclerosing - complications Humans Lymphatic Diseases - complications Lymphatic Diseases - immunology Male Middle Aged |
title | Sclerosing cholangitis and systemic lymphadenopathy |
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