A case of Vogt-Koyanagi-Harada syndrome in a patient affected by Hodgkin's disease
The Vogt-Koyanagi-Harada (VKH) syndrome, a disease of unknown origin, characterized by inflammation of the uveal tract, retina and meninges, was observed in a patient with Hodgkin's disease (HD) who had been treated with chemotherapy and radiotherapy. Ten years later the patient developed a clu...
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| Veröffentlicht in: | Journal of neurology 1989-07, Vol.236 (5), p.303-304 |
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| container_title | Journal of neurology |
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| creator | CIPRIANI, D LANDONIO, G CANEPARI, C |
| description | The Vogt-Koyanagi-Harada (VKH) syndrome, a disease of unknown origin, characterized by inflammation of the uveal tract, retina and meninges, was observed in a patient with Hodgkin's disease (HD) who had been treated with chemotherapy and radiotherapy. Ten years later the patient developed a cluster of neurological symptoms and signs (fever, pain, bilateral hypoacousia, dizziness, uveitis and psychiatric disorder) which were initially interpreted as a relapse of HD. The diagnosis of VKH syndrome was thereafter suspected from the clinical findings, response to therapy and further evolution. During the follow-up (14 months) the patient showed a varying course; hypoacousia remained unaltered while uveitis recurred and only a partial improvement was obtained by immunosuppressive therapy. |
| doi_str_mv | 10.1007/BF00314462 |
| format | Article |
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Ten years later the patient developed a cluster of neurological symptoms and signs (fever, pain, bilateral hypoacousia, dizziness, uveitis and psychiatric disorder) which were initially interpreted as a relapse of HD. The diagnosis of VKH syndrome was thereafter suspected from the clinical findings, response to therapy and further evolution. During the follow-up (14 months) the patient showed a varying course; hypoacousia remained unaltered while uveitis recurred and only a partial improvement was obtained by immunosuppressive therapy.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/BF00314462</identifier><identifier>PMID: 2760648</identifier><identifier>CODEN: JNRYA9</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Biological and medical sciences ; Female ; Hematologic and hematopoietic diseases ; Hodgkin Disease - complications ; Humans ; Leukemias. Malignant lymphomas. 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Ten years later the patient developed a cluster of neurological symptoms and signs (fever, pain, bilateral hypoacousia, dizziness, uveitis and psychiatric disorder) which were initially interpreted as a relapse of HD. The diagnosis of VKH syndrome was thereafter suspected from the clinical findings, response to therapy and further evolution. During the follow-up (14 months) the patient showed a varying course; hypoacousia remained unaltered while uveitis recurred and only a partial improvement was obtained by immunosuppressive therapy.</description><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hodgkin Disease - complications</subject><subject>Humans</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Uveitis - complications</subject><subject>Uveomeningoencephalitic Syndrome - complications</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1LwzAchoMoc04v3oUcREGo5rvJcQ7nxIEg6rX8mqSj2o-ZdIf-91ZW9PQenofn8CJ0TsktJSS9u18SwqkQih2gKRWcJVRIc4imhAuSSC7FMTqJ8ZMQogcwQROWKqKEnqLXObYQPW4L_NFuuuS57aGBTZmsIIADHPvGhbb2uGww4C10pW86DEXhbecdznu8at3mq2yuI3Zl9EPrFB0VUEV_Nu4MvS8f3harZP3y-LSYrxPLKe0S6ZVkRuaScc4LyDUYxyjTwIxIqSFSKukd5UprLY11whDncrAFy1MrU8tn6Grf3Yb2e-djl9VltL6qoPHtLmapoVxrIwfxZi_a0MYYfJFtQ1lD6DNKst8Ds_8DB_lirO7y2rs_dXxs4Jcjh2ihKgI0tox_mpJGK0X4D5KCdVA</recordid><startdate>198907</startdate><enddate>198907</enddate><creator>CIPRIANI, D</creator><creator>LANDONIO, G</creator><creator>CANEPARI, C</creator><general>Springer</general><scope>IQODW</scope><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></search><sort><creationdate>198907</creationdate><title>A case of Vogt-Koyanagi-Harada syndrome in a patient affected by Hodgkin's disease</title><author>CIPRIANI, D ; LANDONIO, G ; CANEPARI, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-5e65295b52333fab8a9d2128a29471905565ed13688859cd490ddbacf2b7c57c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hodgkin Disease - complications</topic><topic>Humans</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Uveitis - complications</topic><topic>Uveomeningoencephalitic Syndrome - complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CIPRIANI, D</creatorcontrib><creatorcontrib>LANDONIO, G</creatorcontrib><creatorcontrib>CANEPARI, C</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CIPRIANI, D</au><au>LANDONIO, G</au><au>CANEPARI, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of Vogt-Koyanagi-Harada syndrome in a patient affected by Hodgkin's disease</atitle><jtitle>Journal of neurology</jtitle><addtitle>J Neurol</addtitle><date>1989-07</date><risdate>1989</risdate><volume>236</volume><issue>5</issue><spage>303</spage><epage>304</epage><pages>303-304</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><coden>JNRYA9</coden><abstract>The Vogt-Koyanagi-Harada (VKH) syndrome, a disease of unknown origin, characterized by inflammation of the uveal tract, retina and meninges, was observed in a patient with Hodgkin's disease (HD) who had been treated with chemotherapy and radiotherapy. 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| ispartof | Journal of neurology, 1989-07, Vol.236 (5), p.303-304 |
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| language | eng |
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| subjects | Biological and medical sciences Female Hematologic and hematopoietic diseases Hodgkin Disease - complications Humans Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Medical sciences Middle Aged Uveitis - complications Uveomeningoencephalitic Syndrome - complications |
| title | A case of Vogt-Koyanagi-Harada syndrome in a patient affected by Hodgkin's disease |
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