A case report of progressive multifocal leukoencephalopathy during steroid treatment for ANCA-associated renal vasculitis
Case report: an 80-year-old woman presented with rapidly progressive glomerulonephritis and was admitted to our hospital. Myeloperoxidase-specific antineutrophil cytoplasmic antibody (MPO-ANCA) was positive. We diagnosed ANCA-associated renal vasculitis (ANCA-RV). Treatment was initiated with intrav...
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Veröffentlicht in: | CEN case reports 2020-11, Vol.9 (4), p.354-358 |
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creator | Tawara, Takashi Kai, Hirayasu Kageyama, Mikiko Akiyama, Tomoki Matsunaga, Takahiro Sakuma, Aki Ishii, Ryota Tsunoda, Ryouya Kawamura, Tetusya Fujita, Akiko Kaneko, Shuzo Morito, Naoki Saito, Chie Usui, Joichi Yamagata, Kunihiro |
description | Case report: an 80-year-old woman presented with rapidly progressive glomerulonephritis and was admitted to our hospital. Myeloperoxidase-specific antineutrophil cytoplasmic antibody (MPO-ANCA) was positive. We diagnosed ANCA-associated renal vasculitis (ANCA-RV). Treatment was initiated with intravenous methylprednisolone pulse therapy, followed by prednisolone (PSL) at 30 mg/day. We gradually reduced the PSL dose to 7.5 mg/day over 6 months. At that time, the patient developed disturbances of consciousness which progressed subacutely. MRI revealed regions of patchy white matter with an increased signal on T2-weighted, fluid attenuated inversion recovery (FLAIR) sequences and diffusion-weighted sequences. JC virus DNA was detected in the cerebrospinal fluid (CSF) by polymerase chain reaction (PCR), leading to a diagnosis of progressive multifocal leukoencephalopathy (PML). PML is a rare infectious demyelinating disease of the central nervous system caused by JC virus infection, occurring in highly immunosuppressed individuals such as HIV-infected patients and patients using some biological agents, and having a very poor prognosis. In the present case, PML may have been associated with steroid use, although there are very few case reports of PML in patients taking only steroids. We report progressive multifocal leukoencephalopathy during steroid treatment of ANCA-RV. When patients show progressive disturbance of consciousness during treatment for ANCA-RV, we need to take PML into consideration for differential diagnosis. |
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Myeloperoxidase-specific antineutrophil cytoplasmic antibody (MPO-ANCA) was positive. We diagnosed ANCA-associated renal vasculitis (ANCA-RV). Treatment was initiated with intravenous methylprednisolone pulse therapy, followed by prednisolone (PSL) at 30 mg/day. We gradually reduced the PSL dose to 7.5 mg/day over 6 months. At that time, the patient developed disturbances of consciousness which progressed subacutely. MRI revealed regions of patchy white matter with an increased signal on T2-weighted, fluid attenuated inversion recovery (FLAIR) sequences and diffusion-weighted sequences. JC virus DNA was detected in the cerebrospinal fluid (CSF) by polymerase chain reaction (PCR), leading to a diagnosis of progressive multifocal leukoencephalopathy (PML). PML is a rare infectious demyelinating disease of the central nervous system caused by JC virus infection, occurring in highly immunosuppressed individuals such as HIV-infected patients and patients using some biological agents, and having a very poor prognosis. In the present case, PML may have been associated with steroid use, although there are very few case reports of PML in patients taking only steroids. We report progressive multifocal leukoencephalopathy during steroid treatment of ANCA-RV. When patients show progressive disturbance of consciousness during treatment for ANCA-RV, we need to take PML into consideration for differential diagnosis.</description><identifier>ISSN: 2192-4449</identifier><identifier>EISSN: 2192-4449</identifier><identifier>DOI: 10.1007/s13730-020-00482-w</identifier><identifier>PMID: 32388828</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Case Report ; Medicine ; Medicine & Public Health ; Nephrology ; Urology</subject><ispartof>CEN case reports, 2020-11, Vol.9 (4), p.354-358</ispartof><rights>Japanese Society of Nephrology 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c591t-8e39f65b8ab581408f3d0c06e42b6f15dbe4b9ea6d5765b1117a34d0412fe0013</citedby><cites>FETCH-LOGICAL-c591t-8e39f65b8ab581408f3d0c06e42b6f15dbe4b9ea6d5765b1117a34d0412fe0013</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/PMC7502088/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502088/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,41467,42536,51297,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32388828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tawara, Takashi</creatorcontrib><creatorcontrib>Kai, Hirayasu</creatorcontrib><creatorcontrib>Kageyama, Mikiko</creatorcontrib><creatorcontrib>Akiyama, Tomoki</creatorcontrib><creatorcontrib>Matsunaga, Takahiro</creatorcontrib><creatorcontrib>Sakuma, Aki</creatorcontrib><creatorcontrib>Ishii, Ryota</creatorcontrib><creatorcontrib>Tsunoda, Ryouya</creatorcontrib><creatorcontrib>Kawamura, Tetusya</creatorcontrib><creatorcontrib>Fujita, Akiko</creatorcontrib><creatorcontrib>Kaneko, Shuzo</creatorcontrib><creatorcontrib>Morito, Naoki</creatorcontrib><creatorcontrib>Saito, Chie</creatorcontrib><creatorcontrib>Usui, Joichi</creatorcontrib><creatorcontrib>Yamagata, Kunihiro</creatorcontrib><title>A case report of progressive multifocal leukoencephalopathy during steroid treatment for ANCA-associated renal vasculitis</title><title>CEN case reports</title><addtitle>CEN Case Rep</addtitle><addtitle>CEN Case Rep</addtitle><description>Case report: an 80-year-old woman presented with rapidly progressive glomerulonephritis and was admitted to our hospital. Myeloperoxidase-specific antineutrophil cytoplasmic antibody (MPO-ANCA) was positive. We diagnosed ANCA-associated renal vasculitis (ANCA-RV). Treatment was initiated with intravenous methylprednisolone pulse therapy, followed by prednisolone (PSL) at 30 mg/day. We gradually reduced the PSL dose to 7.5 mg/day over 6 months. At that time, the patient developed disturbances of consciousness which progressed subacutely. MRI revealed regions of patchy white matter with an increased signal on T2-weighted, fluid attenuated inversion recovery (FLAIR) sequences and diffusion-weighted sequences. JC virus DNA was detected in the cerebrospinal fluid (CSF) by polymerase chain reaction (PCR), leading to a diagnosis of progressive multifocal leukoencephalopathy (PML). PML is a rare infectious demyelinating disease of the central nervous system caused by JC virus infection, occurring in highly immunosuppressed individuals such as HIV-infected patients and patients using some biological agents, and having a very poor prognosis. In the present case, PML may have been associated with steroid use, although there are very few case reports of PML in patients taking only steroids. We report progressive multifocal leukoencephalopathy during steroid treatment of ANCA-RV. When patients show progressive disturbance of consciousness during treatment for ANCA-RV, we need to take PML into consideration for differential diagnosis.</description><subject>Case Report</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nephrology</subject><subject>Urology</subject><issn>2192-4449</issn><issn>2192-4449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kU9v1DAQxSNERau2X4AD8pFLwP-ycS5IqxUFpAou5Ww5znjXxYmDx9lqvz3ebqnKhYNlS_PmN-P3quotox8Ype1HZKIVtKa8HCoVrx9eVRecdbyWUnavX7zPq2vEe0opE5I2tHtTnQsulFJcXVSHNbEGgSSYY8okOjKnuE2A6PdAxiVk76I1gQRYfkWYLMw7E-Js8u5AhiX5aUswQ4p-IDmBySNMmbiYyPr7Zl0bxGi9yTCUCVPB7A3aJfjs8ao6cyYgXD_dl9XPm893m6_17Y8v3zbr29o2Hcu1AtG5VdMr0zeKSaqcGKilK5C8XznWDD3IvgOzGpq2yBhjrRFyoJJxB8c_X1afTtx56UcYbNkvmaDn5EeTDjoar_-tTH6nt3Gv26aYq1QBvH8CpPh7Acx69GghBDNBXFBzSRnjsuNHKT9JbYqICdzzGEb1MTZ9ik0Xsn6MTT-UpncvF3xu-RtSEYiTAOej35D0fVxScRP_h_0DfmmnJQ</recordid><startdate>20201101</startdate><enddate>20201101</enddate><creator>Tawara, Takashi</creator><creator>Kai, Hirayasu</creator><creator>Kageyama, Mikiko</creator><creator>Akiyama, Tomoki</creator><creator>Matsunaga, Takahiro</creator><creator>Sakuma, Aki</creator><creator>Ishii, Ryota</creator><creator>Tsunoda, Ryouya</creator><creator>Kawamura, Tetusya</creator><creator>Fujita, Akiko</creator><creator>Kaneko, Shuzo</creator><creator>Morito, Naoki</creator><creator>Saito, Chie</creator><creator>Usui, Joichi</creator><creator>Yamagata, Kunihiro</creator><general>Springer Singapore</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20201101</creationdate><title>A case report of progressive multifocal leukoencephalopathy during steroid treatment for ANCA-associated renal vasculitis</title><author>Tawara, Takashi ; Kai, Hirayasu ; Kageyama, Mikiko ; Akiyama, Tomoki ; Matsunaga, Takahiro ; Sakuma, Aki ; Ishii, Ryota ; Tsunoda, Ryouya ; Kawamura, Tetusya ; Fujita, Akiko ; Kaneko, Shuzo ; Morito, Naoki ; Saito, Chie ; Usui, Joichi ; Yamagata, Kunihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c591t-8e39f65b8ab581408f3d0c06e42b6f15dbe4b9ea6d5765b1117a34d0412fe0013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Case Report</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nephrology</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tawara, Takashi</creatorcontrib><creatorcontrib>Kai, Hirayasu</creatorcontrib><creatorcontrib>Kageyama, Mikiko</creatorcontrib><creatorcontrib>Akiyama, Tomoki</creatorcontrib><creatorcontrib>Matsunaga, Takahiro</creatorcontrib><creatorcontrib>Sakuma, Aki</creatorcontrib><creatorcontrib>Ishii, Ryota</creatorcontrib><creatorcontrib>Tsunoda, Ryouya</creatorcontrib><creatorcontrib>Kawamura, Tetusya</creatorcontrib><creatorcontrib>Fujita, Akiko</creatorcontrib><creatorcontrib>Kaneko, Shuzo</creatorcontrib><creatorcontrib>Morito, Naoki</creatorcontrib><creatorcontrib>Saito, Chie</creatorcontrib><creatorcontrib>Usui, Joichi</creatorcontrib><creatorcontrib>Yamagata, Kunihiro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>CEN case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tawara, Takashi</au><au>Kai, Hirayasu</au><au>Kageyama, Mikiko</au><au>Akiyama, Tomoki</au><au>Matsunaga, Takahiro</au><au>Sakuma, Aki</au><au>Ishii, Ryota</au><au>Tsunoda, Ryouya</au><au>Kawamura, Tetusya</au><au>Fujita, Akiko</au><au>Kaneko, Shuzo</au><au>Morito, Naoki</au><au>Saito, Chie</au><au>Usui, Joichi</au><au>Yamagata, Kunihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case report of progressive multifocal leukoencephalopathy during steroid treatment for ANCA-associated renal vasculitis</atitle><jtitle>CEN case reports</jtitle><stitle>CEN Case Rep</stitle><addtitle>CEN Case Rep</addtitle><date>2020-11-01</date><risdate>2020</risdate><volume>9</volume><issue>4</issue><spage>354</spage><epage>358</epage><pages>354-358</pages><issn>2192-4449</issn><eissn>2192-4449</eissn><abstract>Case report: an 80-year-old woman presented with rapidly progressive glomerulonephritis and was admitted to our hospital. Myeloperoxidase-specific antineutrophil cytoplasmic antibody (MPO-ANCA) was positive. We diagnosed ANCA-associated renal vasculitis (ANCA-RV). Treatment was initiated with intravenous methylprednisolone pulse therapy, followed by prednisolone (PSL) at 30 mg/day. We gradually reduced the PSL dose to 7.5 mg/day over 6 months. At that time, the patient developed disturbances of consciousness which progressed subacutely. MRI revealed regions of patchy white matter with an increased signal on T2-weighted, fluid attenuated inversion recovery (FLAIR) sequences and diffusion-weighted sequences. JC virus DNA was detected in the cerebrospinal fluid (CSF) by polymerase chain reaction (PCR), leading to a diagnosis of progressive multifocal leukoencephalopathy (PML). PML is a rare infectious demyelinating disease of the central nervous system caused by JC virus infection, occurring in highly immunosuppressed individuals such as HIV-infected patients and patients using some biological agents, and having a very poor prognosis. In the present case, PML may have been associated with steroid use, although there are very few case reports of PML in patients taking only steroids. We report progressive multifocal leukoencephalopathy during steroid treatment of ANCA-RV. When patients show progressive disturbance of consciousness during treatment for ANCA-RV, we need to take PML into consideration for differential diagnosis.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>32388828</pmid><doi>10.1007/s13730-020-00482-w</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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title | A case report of progressive multifocal leukoencephalopathy during steroid treatment for ANCA-associated renal vasculitis |
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