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Adult-onset Still's disease with disseminated intravascular coagulation and multiple organ dysfunctions dramatically treated with cyclosporine A
Severe systemic manifestations of adult onset Still's disease (AOSD) are often fatal and occasionally related to hemophagocytic syndrome (HS). We describe the case of a 49-yr-old woman with AOSD presenting with non-remitting high fever, confusion, jaundice, hepatosplenomegaly, serositis, azotem...
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Published in: | Journal of Korean medical science 2004-02, Vol.19 (1), p.137-141 |
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creator | Park, Jae-Hong Bae, Joong Ho Choi, Yeon-Soo Lee, Hye-Soon Jun, Jae-Bum Jung, Sungsoo Yoo, Dae-Hyun Bae, Sang-Cheol Kim, Tae-Hwan |
description | Severe systemic manifestations of adult onset Still's disease (AOSD) are often fatal and occasionally related to hemophagocytic syndrome (HS). We describe the case of a 49-yr-old woman with AOSD presenting with non-remitting high fever, confusion, jaundice, hepatosplenomegaly, serositis, azotemia, pancytopenia, coagulopathy with disseminated intravascular coagulation (DIC), hyperferritinemia, acute acalculous cholecystitis and ileocolitis noted in computed tomographic images. The patient had a history of herpes zoster developed prior to the admission, but there is no history of diarrhea or abdominal pain. Although bone marrow examination was not performed due to hemorrhagic diathesis, we suspected AOSD-associated HS on the basis of clinical course without detectable infectious agents in cultures or serologic studies. Intravenous immunoglobulin, pulse methylprednisolone, oral cyclosporine A (CsA) and ceftriaxone brought about transient improvement of fever and confusion, but the disease progressed. After increasing CsA dose, all previously mentioned abnormalities disappeared rapidly. Accordingly, we believe that DIC and multiple organ dysfunctions might have been the complications of HS but not that of sepsis, and that CsA can be used as a first-line therapy in case of life-threatening situations. |
doi_str_mv | 10.3346/jkms.2004.19.1.137 |
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We describe the case of a 49-yr-old woman with AOSD presenting with non-remitting high fever, confusion, jaundice, hepatosplenomegaly, serositis, azotemia, pancytopenia, coagulopathy with disseminated intravascular coagulation (DIC), hyperferritinemia, acute acalculous cholecystitis and ileocolitis noted in computed tomographic images. The patient had a history of herpes zoster developed prior to the admission, but there is no history of diarrhea or abdominal pain. Although bone marrow examination was not performed due to hemorrhagic diathesis, we suspected AOSD-associated HS on the basis of clinical course without detectable infectious agents in cultures or serologic studies. Intravenous immunoglobulin, pulse methylprednisolone, oral cyclosporine A (CsA) and ceftriaxone brought about transient improvement of fever and confusion, but the disease progressed. After increasing CsA dose, all previously mentioned abnormalities disappeared rapidly. Accordingly, we believe that DIC and multiple organ dysfunctions might have been the complications of HS but not that of sepsis, and that CsA can be used as a first-line therapy in case of life-threatening situations.</description><identifier>ISSN: 1011-8934</identifier><identifier>EISSN: 1598-6357</identifier><identifier>DOI: 10.3346/jkms.2004.19.1.137</identifier><identifier>PMID: 14966357</identifier><language>eng</language><publisher>Korea (South): The Korean Academy of Medical Sciences</publisher><subject>Case Report ; Colon - diagnostic imaging ; Cyclosporine - therapeutic use ; Female ; Humans ; Immunosuppressive Agents - therapeutic use ; Middle Aged ; Multiple Organ Failure ; Still's Disease, Adult-Onset - diagnosis ; Still's Disease, Adult-Onset - pathology ; Time Factors ; Tomography, X-Ray Computed</subject><ispartof>Journal of Korean medical science, 2004-02, Vol.19 (1), p.137-141</ispartof><rights>Copyright © 2004 The Korean Academy of Medical Sciences 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-cc61df19bd2fea0c3c226f9208450b23d2c60f6a9a85cf07947d937ce75749473</citedby><cites>FETCH-LOGICAL-c398t-cc61df19bd2fea0c3c226f9208450b23d2c60f6a9a85cf07947d937ce75749473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822251/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822251/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14966357$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Jae-Hong</creatorcontrib><creatorcontrib>Bae, Joong Ho</creatorcontrib><creatorcontrib>Choi, Yeon-Soo</creatorcontrib><creatorcontrib>Lee, Hye-Soon</creatorcontrib><creatorcontrib>Jun, Jae-Bum</creatorcontrib><creatorcontrib>Jung, Sungsoo</creatorcontrib><creatorcontrib>Yoo, Dae-Hyun</creatorcontrib><creatorcontrib>Bae, Sang-Cheol</creatorcontrib><creatorcontrib>Kim, Tae-Hwan</creatorcontrib><title>Adult-onset Still's disease with disseminated intravascular coagulation and multiple organ dysfunctions dramatically treated with cyclosporine A</title><title>Journal of Korean medical science</title><addtitle>J Korean Med Sci</addtitle><description>Severe systemic manifestations of adult onset Still's disease (AOSD) are often fatal and occasionally related to hemophagocytic syndrome (HS). We describe the case of a 49-yr-old woman with AOSD presenting with non-remitting high fever, confusion, jaundice, hepatosplenomegaly, serositis, azotemia, pancytopenia, coagulopathy with disseminated intravascular coagulation (DIC), hyperferritinemia, acute acalculous cholecystitis and ileocolitis noted in computed tomographic images. The patient had a history of herpes zoster developed prior to the admission, but there is no history of diarrhea or abdominal pain. Although bone marrow examination was not performed due to hemorrhagic diathesis, we suspected AOSD-associated HS on the basis of clinical course without detectable infectious agents in cultures or serologic studies. Intravenous immunoglobulin, pulse methylprednisolone, oral cyclosporine A (CsA) and ceftriaxone brought about transient improvement of fever and confusion, but the disease progressed. After increasing CsA dose, all previously mentioned abnormalities disappeared rapidly. Accordingly, we believe that DIC and multiple organ dysfunctions might have been the complications of HS but not that of sepsis, and that CsA can be used as a first-line therapy in case of life-threatening situations.</description><subject>Case Report</subject><subject>Colon - diagnostic imaging</subject><subject>Cyclosporine - therapeutic use</subject><subject>Female</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Middle Aged</subject><subject>Multiple Organ Failure</subject><subject>Still's Disease, Adult-Onset - diagnosis</subject><subject>Still's Disease, Adult-Onset - pathology</subject><subject>Time Factors</subject><subject>Tomography, X-Ray Computed</subject><issn>1011-8934</issn><issn>1598-6357</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpVkU1v1DAQhi0EoqXwBzggn-CU4I84iS9Iq6p8SJU40J4t79jZujj2YjtF-y_4yXXaFdDTzGjeeWZGL0JvKWk57_qPtz_n3DJCupbKlraUD8_QKRVybHouhuc1J5Q2o-TdCXqV8y0hTAjGX6IT2sl-1ZyiPxuz-NLEkG3BP4rz_kPGxmWrs8W_XblZi2xnF3SxBrtQkr7TGRavE4aodzUpLgasg8FzRbm9tzimnQ7YHPK0BFjblZn0XJWgvT_gkuwD7mEBHMDHvI_JBYs3r9GLSfts3xzjGbr-fHF1_rW5_P7l2_nmsgEux9IA9NRMVG4Nm6wmwIGxfpKMjJ0gW8YNg55MvZZ6FDCRQXaDkXwAO4ihqwU_Q58euftlO1sDdv3Mq31ys04HFbVTTzvB3ahdvFNsZIwJWgHvj4AUfy02FzW7DNZ7HWxcshoJFYKIvgrZoxBSzDnZ6e8SStRqpFqNVKuRikpFVTWyDr37_7x_I0fn-D13S6CB</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Park, Jae-Hong</creator><creator>Bae, Joong Ho</creator><creator>Choi, Yeon-Soo</creator><creator>Lee, Hye-Soon</creator><creator>Jun, Jae-Bum</creator><creator>Jung, Sungsoo</creator><creator>Yoo, Dae-Hyun</creator><creator>Bae, Sang-Cheol</creator><creator>Kim, Tae-Hwan</creator><general>The Korean Academy of Medical Sciences</general><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>5PM</scope></search><sort><creationdate>20040201</creationdate><title>Adult-onset Still's disease with disseminated intravascular coagulation and multiple organ dysfunctions dramatically treated with cyclosporine A</title><author>Park, Jae-Hong ; Bae, Joong Ho ; Choi, Yeon-Soo ; Lee, Hye-Soon ; Jun, Jae-Bum ; Jung, Sungsoo ; Yoo, Dae-Hyun ; Bae, Sang-Cheol ; Kim, Tae-Hwan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-cc61df19bd2fea0c3c226f9208450b23d2c60f6a9a85cf07947d937ce75749473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Case Report</topic><topic>Colon - diagnostic imaging</topic><topic>Cyclosporine - therapeutic use</topic><topic>Female</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Middle Aged</topic><topic>Multiple Organ Failure</topic><topic>Still's Disease, Adult-Onset - diagnosis</topic><topic>Still's Disease, Adult-Onset - pathology</topic><topic>Time Factors</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Jae-Hong</creatorcontrib><creatorcontrib>Bae, Joong Ho</creatorcontrib><creatorcontrib>Choi, Yeon-Soo</creatorcontrib><creatorcontrib>Lee, Hye-Soon</creatorcontrib><creatorcontrib>Jun, Jae-Bum</creatorcontrib><creatorcontrib>Jung, Sungsoo</creatorcontrib><creatorcontrib>Yoo, Dae-Hyun</creatorcontrib><creatorcontrib>Bae, Sang-Cheol</creatorcontrib><creatorcontrib>Kim, Tae-Hwan</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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Korean medical science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Jae-Hong</au><au>Bae, Joong Ho</au><au>Choi, Yeon-Soo</au><au>Lee, Hye-Soon</au><au>Jun, Jae-Bum</au><au>Jung, Sungsoo</au><au>Yoo, Dae-Hyun</au><au>Bae, Sang-Cheol</au><au>Kim, Tae-Hwan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adult-onset Still's disease with disseminated intravascular coagulation and multiple organ dysfunctions dramatically treated with cyclosporine A</atitle><jtitle>Journal of Korean medical science</jtitle><addtitle>J Korean Med Sci</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>19</volume><issue>1</issue><spage>137</spage><epage>141</epage><pages>137-141</pages><issn>1011-8934</issn><eissn>1598-6357</eissn><abstract>Severe systemic manifestations of adult onset Still's disease (AOSD) are often fatal and occasionally related to hemophagocytic syndrome (HS). We describe the case of a 49-yr-old woman with AOSD presenting with non-remitting high fever, confusion, jaundice, hepatosplenomegaly, serositis, azotemia, pancytopenia, coagulopathy with disseminated intravascular coagulation (DIC), hyperferritinemia, acute acalculous cholecystitis and ileocolitis noted in computed tomographic images. The patient had a history of herpes zoster developed prior to the admission, but there is no history of diarrhea or abdominal pain. Although bone marrow examination was not performed due to hemorrhagic diathesis, we suspected AOSD-associated HS on the basis of clinical course without detectable infectious agents in cultures or serologic studies. Intravenous immunoglobulin, pulse methylprednisolone, oral cyclosporine A (CsA) and ceftriaxone brought about transient improvement of fever and confusion, but the disease progressed. After increasing CsA dose, all previously mentioned abnormalities disappeared rapidly. Accordingly, we believe that DIC and multiple organ dysfunctions might have been the complications of HS but not that of sepsis, and that CsA can be used as a first-line therapy in case of life-threatening situations.</abstract><cop>Korea (South)</cop><pub>The Korean Academy of Medical Sciences</pub><pmid>14966357</pmid><doi>10.3346/jkms.2004.19.1.137</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Case Report Colon - diagnostic imaging Cyclosporine - therapeutic use Female Humans Immunosuppressive Agents - therapeutic use Middle Aged Multiple Organ Failure Still's Disease, Adult-Onset - diagnosis Still's Disease, Adult-Onset - pathology Time Factors Tomography, X-Ray Computed |
title | Adult-onset Still's disease with disseminated intravascular coagulation and multiple organ dysfunctions dramatically treated with cyclosporine A |
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