Loading…
Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient
Central nervous system (CNS) vasculitis secondary to chronic parvovirus B19 (B19) infection presenting with recurrent neurological findings is a very rare disorder during childhood. Here we report a 12-year-old boy with a renal transplant who had chronic B19 infection with skin eruptions and recurre...
Saved in:
Published in: | Pediatric nephrology (Berlin, West) West), 2005-04, Vol.20 (4), p.529-533 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3 |
container_end_page | 533 |
container_issue | 4 |
container_start_page | 529 |
container_title | Pediatric nephrology (Berlin, West) |
container_volume | 20 |
creator | Bilge, Ilmay Sadikoğlu, Banu Emre, Sevinç Sirin, Aydan Aydin, Kubilay Tatli, Burak |
description | Central nervous system (CNS) vasculitis secondary to chronic parvovirus B19 (B19) infection presenting with recurrent neurological findings is a very rare disorder during childhood. Here we report a 12-year-old boy with a renal transplant who had chronic B19 infection with skin eruptions and recurrent episodes of encephalopathy with focal neurological deficits. B19 DNA was detected in blood, bone marrow, and skin biopsy specimens. Repeat cranial magnetic resonance (MR) imaging during each episode of encephalopathy showed variable focal findings, and MR angiography revealed vasculitic changes with narrowing of the cerebral arteries. We hypothesized that the CNS vasculitis might be associated with the chronic B19 infection. At the time of his fourth presentation with the same clinical findings, we administered intravenous immunoglobulin (IVIG) (1 g/kg per day, 2 consecutive days), which we continued for 6 months, at monthly intervals. IVIG therapy resulted in remission and has been effective not only for the clearance of B19, but also for the improvement of clinical and radiological findings of CNS vasculitis. We suggest that chronic B19 infection should be considered in immunocompromised patients with suspected CNS vasculitis. IVIG should be considered as a part of the treatment. |
doi_str_mv | 10.1007/s00467-004-1736-1 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_67484446</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A152872390</galeid><sourcerecordid>A152872390</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3</originalsourceid><addsrcrecordid>eNpdkU9v1DAQxS0EokvhA3BBFgduAU_sxMmxrGhBqsSFSr1ZXntMXWXjYDsr9dt3VrtSJS7jP_rN8xs_xj6C-ApC6G9FCNXrhmoDWvYNvGIbULJtYBzuX7ONGCU0QsH9BXtXyqMQYuiG_i27gE4rDb3csLTFuWY78RnzIa2Fl6dScc8Ptrh1ijXSDbo0e5ufeE18sYQdYibyO4w8zgFdjWmmHbd8QR9tzdHxjDOJkvJclsnOlRprpKfeszfBTgU_nNdLdnf948_2Z3P7--bX9uq2cbLTtQHoWhvAaY_oRbCDVr7bKaV2oVdBCq9pAuWDo2O3sx7HEcXgWiWGNsgR5SX7ctJdcvq3YqlmH4vDibwgjWl6rQaS6wn8_B_4mNZM5otp21YSB-JF7a-d0DygnepDSdN6nLyYKzI76FaORxBOoMuplIzBLDnu6e8MCHPMzJwyM1TNMTMD1PPp7GDd7dG_dJxDks8zPpNI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>222367410</pqid></control><display><type>article</type><title>Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient</title><source>Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List</source><creator>Bilge, Ilmay ; Sadikoğlu, Banu ; Emre, Sevinç ; Sirin, Aydan ; Aydin, Kubilay ; Tatli, Burak</creator><creatorcontrib>Bilge, Ilmay ; Sadikoğlu, Banu ; Emre, Sevinç ; Sirin, Aydan ; Aydin, Kubilay ; Tatli, Burak</creatorcontrib><description>Central nervous system (CNS) vasculitis secondary to chronic parvovirus B19 (B19) infection presenting with recurrent neurological findings is a very rare disorder during childhood. Here we report a 12-year-old boy with a renal transplant who had chronic B19 infection with skin eruptions and recurrent episodes of encephalopathy with focal neurological deficits. B19 DNA was detected in blood, bone marrow, and skin biopsy specimens. Repeat cranial magnetic resonance (MR) imaging during each episode of encephalopathy showed variable focal findings, and MR angiography revealed vasculitic changes with narrowing of the cerebral arteries. We hypothesized that the CNS vasculitis might be associated with the chronic B19 infection. At the time of his fourth presentation with the same clinical findings, we administered intravenous immunoglobulin (IVIG) (1 g/kg per day, 2 consecutive days), which we continued for 6 months, at monthly intervals. IVIG therapy resulted in remission and has been effective not only for the clearance of B19, but also for the improvement of clinical and radiological findings of CNS vasculitis. We suggest that chronic B19 infection should be considered in immunocompromised patients with suspected CNS vasculitis. IVIG should be considered as a part of the treatment.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/s00467-004-1736-1</identifier><identifier>PMID: 15747163</identifier><language>eng</language><publisher>Germany: Springer</publisher><subject>Brain Diseases - diagnosis ; Brain Diseases - virology ; Care and treatment ; Case studies ; Central nervous system ; Child ; Chronic Disease ; Health aspects ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Immunosuppression ; Kidney Transplantation - adverse effects ; Magnetic Resonance Angiography ; Magnetic Resonance Imaging ; Male ; Parvoviridae Infections - etiology ; Parvoviridae Infections - therapy ; Parvovirus B19, Human ; Parvovirus infections ; Vasculitis ; Vasculitis, Central Nervous System - virology</subject><ispartof>Pediatric nephrology (Berlin, West), 2005-04, Vol.20 (4), p.529-533</ispartof><rights>COPYRIGHT 2005 Springer</rights><rights>IPNA 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3</citedby><cites>FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15747163$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bilge, Ilmay</creatorcontrib><creatorcontrib>Sadikoğlu, Banu</creatorcontrib><creatorcontrib>Emre, Sevinç</creatorcontrib><creatorcontrib>Sirin, Aydan</creatorcontrib><creatorcontrib>Aydin, Kubilay</creatorcontrib><creatorcontrib>Tatli, Burak</creatorcontrib><title>Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><description>Central nervous system (CNS) vasculitis secondary to chronic parvovirus B19 (B19) infection presenting with recurrent neurological findings is a very rare disorder during childhood. Here we report a 12-year-old boy with a renal transplant who had chronic B19 infection with skin eruptions and recurrent episodes of encephalopathy with focal neurological deficits. B19 DNA was detected in blood, bone marrow, and skin biopsy specimens. Repeat cranial magnetic resonance (MR) imaging during each episode of encephalopathy showed variable focal findings, and MR angiography revealed vasculitic changes with narrowing of the cerebral arteries. We hypothesized that the CNS vasculitis might be associated with the chronic B19 infection. At the time of his fourth presentation with the same clinical findings, we administered intravenous immunoglobulin (IVIG) (1 g/kg per day, 2 consecutive days), which we continued for 6 months, at monthly intervals. IVIG therapy resulted in remission and has been effective not only for the clearance of B19, but also for the improvement of clinical and radiological findings of CNS vasculitis. We suggest that chronic B19 infection should be considered in immunocompromised patients with suspected CNS vasculitis. IVIG should be considered as a part of the treatment.</description><subject>Brain Diseases - diagnosis</subject><subject>Brain Diseases - virology</subject><subject>Care and treatment</subject><subject>Case studies</subject><subject>Central nervous system</subject><subject>Child</subject><subject>Chronic Disease</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunosuppression</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Magnetic Resonance Angiography</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Parvoviridae Infections - etiology</subject><subject>Parvoviridae Infections - therapy</subject><subject>Parvovirus B19, Human</subject><subject>Parvovirus infections</subject><subject>Vasculitis</subject><subject>Vasculitis, Central Nervous System - virology</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpdkU9v1DAQxS0EokvhA3BBFgduAU_sxMmxrGhBqsSFSr1ZXntMXWXjYDsr9dt3VrtSJS7jP_rN8xs_xj6C-ApC6G9FCNXrhmoDWvYNvGIbULJtYBzuX7ONGCU0QsH9BXtXyqMQYuiG_i27gE4rDb3csLTFuWY78RnzIa2Fl6dScc8Ptrh1ijXSDbo0e5ufeE18sYQdYibyO4w8zgFdjWmmHbd8QR9tzdHxjDOJkvJclsnOlRprpKfeszfBTgU_nNdLdnf948_2Z3P7--bX9uq2cbLTtQHoWhvAaY_oRbCDVr7bKaV2oVdBCq9pAuWDo2O3sx7HEcXgWiWGNsgR5SX7ctJdcvq3YqlmH4vDibwgjWl6rQaS6wn8_B_4mNZM5otp21YSB-JF7a-d0DygnepDSdN6nLyYKzI76FaORxBOoMuplIzBLDnu6e8MCHPMzJwyM1TNMTMD1PPp7GDd7dG_dJxDks8zPpNI</recordid><startdate>200504</startdate><enddate>200504</enddate><creator>Bilge, Ilmay</creator><creator>Sadikoğlu, Banu</creator><creator>Emre, Sevinç</creator><creator>Sirin, Aydan</creator><creator>Aydin, Kubilay</creator><creator>Tatli, Burak</creator><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200504</creationdate><title>Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient</title><author>Bilge, Ilmay ; Sadikoğlu, Banu ; Emre, Sevinç ; Sirin, Aydan ; Aydin, Kubilay ; Tatli, Burak</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Brain Diseases - diagnosis</topic><topic>Brain Diseases - virology</topic><topic>Care and treatment</topic><topic>Case studies</topic><topic>Central nervous system</topic><topic>Child</topic><topic>Chronic Disease</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Immunosuppression</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Magnetic Resonance Angiography</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Parvoviridae Infections - etiology</topic><topic>Parvoviridae Infections - therapy</topic><topic>Parvovirus B19, Human</topic><topic>Parvovirus infections</topic><topic>Vasculitis</topic><topic>Vasculitis, Central Nervous System - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bilge, Ilmay</creatorcontrib><creatorcontrib>Sadikoğlu, Banu</creatorcontrib><creatorcontrib>Emre, Sevinç</creatorcontrib><creatorcontrib>Sirin, Aydan</creatorcontrib><creatorcontrib>Aydin, Kubilay</creatorcontrib><creatorcontrib>Tatli, Burak</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric nephrology (Berlin, West)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bilge, Ilmay</au><au>Sadikoğlu, Banu</au><au>Emre, Sevinç</au><au>Sirin, Aydan</au><au>Aydin, Kubilay</au><au>Tatli, Burak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient</atitle><jtitle>Pediatric nephrology (Berlin, West)</jtitle><addtitle>Pediatr Nephrol</addtitle><date>2005-04</date><risdate>2005</risdate><volume>20</volume><issue>4</issue><spage>529</spage><epage>533</epage><pages>529-533</pages><issn>0931-041X</issn><eissn>1432-198X</eissn><abstract>Central nervous system (CNS) vasculitis secondary to chronic parvovirus B19 (B19) infection presenting with recurrent neurological findings is a very rare disorder during childhood. Here we report a 12-year-old boy with a renal transplant who had chronic B19 infection with skin eruptions and recurrent episodes of encephalopathy with focal neurological deficits. B19 DNA was detected in blood, bone marrow, and skin biopsy specimens. Repeat cranial magnetic resonance (MR) imaging during each episode of encephalopathy showed variable focal findings, and MR angiography revealed vasculitic changes with narrowing of the cerebral arteries. We hypothesized that the CNS vasculitis might be associated with the chronic B19 infection. At the time of his fourth presentation with the same clinical findings, we administered intravenous immunoglobulin (IVIG) (1 g/kg per day, 2 consecutive days), which we continued for 6 months, at monthly intervals. IVIG therapy resulted in remission and has been effective not only for the clearance of B19, but also for the improvement of clinical and radiological findings of CNS vasculitis. We suggest that chronic B19 infection should be considered in immunocompromised patients with suspected CNS vasculitis. IVIG should be considered as a part of the treatment.</abstract><cop>Germany</cop><pub>Springer</pub><pmid>15747163</pmid><doi>10.1007/s00467-004-1736-1</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0931-041X |
ispartof | Pediatric nephrology (Berlin, West), 2005-04, Vol.20 (4), p.529-533 |
issn | 0931-041X 1432-198X |
language | eng |
recordid | cdi_proquest_miscellaneous_67484446 |
source | Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List |
subjects | Brain Diseases - diagnosis Brain Diseases - virology Care and treatment Case studies Central nervous system Child Chronic Disease Health aspects Humans Immunoglobulins, Intravenous - therapeutic use Immunosuppression Kidney Transplantation - adverse effects Magnetic Resonance Angiography Magnetic Resonance Imaging Male Parvoviridae Infections - etiology Parvoviridae Infections - therapy Parvovirus B19, Human Parvovirus infections Vasculitis Vasculitis, Central Nervous System - virology |
title | Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T12%3A13%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Central%20nervous%20system%20vasculitis%20secondary%20to%20parvovirus%20B19%20infection%20in%20a%20pediatric%20renal%20transplant%20patient&rft.jtitle=Pediatric%20nephrology%20(Berlin,%20West)&rft.au=Bilge,%20Ilmay&rft.date=2005-04&rft.volume=20&rft.issue=4&rft.spage=529&rft.epage=533&rft.pages=529-533&rft.issn=0931-041X&rft.eissn=1432-198X&rft_id=info:doi/10.1007/s00467-004-1736-1&rft_dat=%3Cgale_proqu%3EA152872390%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c357t-1152af1c7deed0fa874d5b444bf64f30d75744dfcf645bade99e08c24082f39e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=222367410&rft_id=info:pmid/15747163&rft_galeid=A152872390&rfr_iscdi=true |