Acquired haemophilia in South Australia: a case series
Of eight cases of acquired haemophilia presenting over an 8‐year period, six received immunosuppressive treatment, five with cyclophosphamide, vincristine and prednisolone (CVP). Five patients (four on immunosuppressive treatment) entered remission, two patients died and one was lost to follow up. I...
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| Veröffentlicht in: | Internal medicine journal 2001-12, Vol.31 (9), p.556-559 |
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| container_title | Internal medicine journal |
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| creator | Burnet, S. P. Duncan, E. M. Lloyd, J. V. Han, P. |
| description | Of eight cases of acquired haemophilia presenting over an 8‐year period, six received immunosuppressive treatment, five with cyclophosphamide, vincristine and prednisolone (CVP). Five patients (four on immunosuppressive treatment) entered remission, two patients died and one was lost to follow up. Initially, the remissions were only partial. The median duration until partial remission was 10 weeks (range 1–55 weeks) and until complete remission was 35 weeks (range 2–59 weeks). Partial remission may proceed to complete remission without further chemotherapy. (Intern Med J 2001; 31: 556–559) |
| doi_str_mv | 10.1046/j.1445-5994.2001.00127.x |
| format | Article |
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P.</creatorcontrib><creatorcontrib>Duncan, E. M.</creatorcontrib><creatorcontrib>Lloyd, J. V.</creatorcontrib><creatorcontrib>Han, P.</creatorcontrib><title>Acquired haemophilia in South Australia: a case series</title><title>Internal medicine journal</title><addtitle>Intern Med J</addtitle><description>Of eight cases of acquired haemophilia presenting over an 8‐year period, six received immunosuppressive treatment, five with cyclophosphamide, vincristine and prednisolone (CVP). Five patients (four on immunosuppressive treatment) entered remission, two patients died and one was lost to follow up. Initially, the remissions were only partial. The median duration until partial remission was 10 weeks (range 1–55 weeks) and until complete remission was 35 weeks (range 2–59 weeks). Partial remission may proceed to complete remission without further chemotherapy. (Intern Med J 2001; 31: 556–559)</description><subject>acquired haemophilia A</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>case series</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hemophilia A - drug therapy</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>partial remission</subject><subject>Platelet diseases and coagulopathies</subject><subject>Remission Induction</subject><subject>South Australia</subject><subject>Time Factors</subject><subject>treatment</subject><subject>Treatment Outcome</subject><issn>1444-0903</issn><issn>1445-5994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1v2zAMhoVhxdJ2-wuDL9vNrmTJoj3skhXrR9q1h27IUaBlGlHmxKkUo-m_r9IE6bUHQYT4vBTxMJYIngmu9Nk8E0oVaVFVKss5F1k8OWSbD-z40Pj4WquUV1yO2EkI8wiBrNQnNhICNJQgj5ke28fBeWqSGdKiX81c5zBxy-ShH9azZDyEtcf49CPBxGKgJJB3FD6zoxa7QF_29yn7d_H77_lVent_eX0-vk2tKnNINQlFVQnIWy6oEDWSrXVdlw01BeoWLKFqlMplhagV5E3DOUIONVQRbOQp-76bu_L940BhbRYuWOo6XFI_BAO51CUUEMFyB1rfh-CpNSvvFuifjeBm68zMzVaN2aoxW2fm1ZnZxOjX_R9DvaDmLbiXFIFvewCDxa71uLQuvHFKqEKWOnI_d9yT6-j53QuY6z-TWMR4uou7sKbNIY7-v9EgoTDTu0sj7yYXxfTXjeHyBRLYlcc</recordid><startdate>200112</startdate><enddate>200112</enddate><creator>Burnet, S. 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P.</creatorcontrib><creatorcontrib>Duncan, E. M.</creatorcontrib><creatorcontrib>Lloyd, J. V.</creatorcontrib><creatorcontrib>Han, P.</creatorcontrib><collection>Istex</collection><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>Internal medicine journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burnet, S. P.</au><au>Duncan, E. M.</au><au>Lloyd, J. V.</au><au>Han, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acquired haemophilia in South Australia: a case series</atitle><jtitle>Internal medicine journal</jtitle><addtitle>Intern Med J</addtitle><date>2001-12</date><risdate>2001</risdate><volume>31</volume><issue>9</issue><spage>556</spage><epage>559</epage><pages>556-559</pages><issn>1444-0903</issn><eissn>1445-5994</eissn><abstract>Of eight cases of acquired haemophilia presenting over an 8‐year period, six received immunosuppressive treatment, five with cyclophosphamide, vincristine and prednisolone (CVP). Five patients (four on immunosuppressive treatment) entered remission, two patients died and one was lost to follow up. Initially, the remissions were only partial. The median duration until partial remission was 10 weeks (range 1–55 weeks) and until complete remission was 35 weeks (range 2–59 weeks). Partial remission may proceed to complete remission without further chemotherapy. 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| identifier | ISSN: 1444-0903 |
| ispartof | Internal medicine journal, 2001-12, Vol.31 (9), p.556-559 |
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| language | eng |
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| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | acquired haemophilia A Adult Aged Aged, 80 and over Biological and medical sciences case series Female Hematologic and hematopoietic diseases Hemophilia A - drug therapy Humans Immunosuppressive Agents - therapeutic use Male Medical sciences Middle Aged partial remission Platelet diseases and coagulopathies Remission Induction South Australia Time Factors treatment Treatment Outcome |
| title | Acquired haemophilia in South Australia: a case series |
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