Chronic anemia as a complication of parvovirus B19 infection in a pediatric kidney transplant patient
This is a report of unexplained anemia that persisted for 4 months in an adolescent renal transplant patient receiving immunosuppression that included prednisone, tacrolimus, and mycophenolate mofetil. This patient required monthly blood transfusions for fatigue, palpitations, and hematocrit levels...
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Veröffentlicht in: | Pediatric nephrology (Berlin, West) West), 1997-06, Vol.11 (3), p.355-357 |
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description | This is a report of unexplained anemia that persisted for 4 months in an adolescent renal transplant patient receiving immunosuppression that included prednisone, tacrolimus, and mycophenolate mofetil. This patient required monthly blood transfusions for fatigue, palpitations, and hematocrit levels between 15% and 17%. In addition, his posttransplant course was notable for the development of insulin-dependent diabetes mellitus. While receiving low-dose prednisone, he was switched from tacrolimus to cyclosporin and tapered off insulin injections over the next 2 months. At 4.5 months post-transplantation, further diagnostic evaluation was suggestive of parvovirus B19 infection as the cause for our patient's chronic anemia. After testing negative for serum-specific parvovirus B19 IgM and IgG antibodies, parvovirus B19 infection was detected in blood by the polymerase chain reaction. Treatment with intravenous immunoglobulin (1 g/kg per day x 2 days) resulted in normalization of both his reticulocyte count and hematocrit within 6 weeks. At 4 months after receiving the immunoglobulin infusion, he has maintained a normal hematocrit level and stable renal function without requiring further blood transfusions. |
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S</creator><creatorcontrib>MATHIAS, R. S</creatorcontrib><description>This is a report of unexplained anemia that persisted for 4 months in an adolescent renal transplant patient receiving immunosuppression that included prednisone, tacrolimus, and mycophenolate mofetil. This patient required monthly blood transfusions for fatigue, palpitations, and hematocrit levels between 15% and 17%. In addition, his posttransplant course was notable for the development of insulin-dependent diabetes mellitus. While receiving low-dose prednisone, he was switched from tacrolimus to cyclosporin and tapered off insulin injections over the next 2 months. At 4.5 months post-transplantation, further diagnostic evaluation was suggestive of parvovirus B19 infection as the cause for our patient's chronic anemia. After testing negative for serum-specific parvovirus B19 IgM and IgG antibodies, parvovirus B19 infection was detected in blood by the polymerase chain reaction. Treatment with intravenous immunoglobulin (1 g/kg per day x 2 days) resulted in normalization of both his reticulocyte count and hematocrit within 6 weeks. At 4 months after receiving the immunoglobulin infusion, he has maintained a normal hematocrit level and stable renal function without requiring further blood transfusions.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/s004670050296</identifier><identifier>PMID: 9203192</identifier><identifier>CODEN: PENED3</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Adolescent ; Anemia ; Anemia - blood ; Anemia - etiology ; Biological and medical sciences ; Blood transfusion ; Blood transfusions ; Chronic Disease ; Chronic infection ; Diabetes mellitus (insulin dependent) ; Hematocrit ; Humans ; Immunoglobulin G ; Immunoglobulin M ; Immunoglobulins ; Immunosuppression ; Immunosuppressive Agents - adverse effects ; Immunosuppressive Agents - therapeutic use ; Infections ; Insulin ; Intravenous administration ; Kidney Function Tests ; Kidney transplantation ; Kidney Transplantation - physiology ; Kidney transplants ; Male ; Medical sciences ; Mycophenolate mofetil ; Mycophenolic acid ; Parvoviridae Infections - blood ; Parvovirus B19, Human ; Parvoviruses ; Patients ; Pediatrics ; Polymerase Chain Reaction ; Prednisone ; Renal function ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Tacrolimus ; Transplants & implants</subject><ispartof>Pediatric nephrology (Berlin, West), 1997-06, Vol.11 (3), p.355-357</ispartof><rights>1997 INIST-CNRS</rights><rights>IPNA - International Pediatric Nephrology Association New York, USA 1997</rights><rights>IPNA - International Pediatric Nephrology Association New York, USA 1997.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-6b5c43f3a0c79bde848dfd8ac8618caaf89a3eefe1b604481a4a22e4d4fd94f23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2698854$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9203192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MATHIAS, R. S</creatorcontrib><title>Chronic anemia as a complication of parvovirus B19 infection in a pediatric kidney transplant patient</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><description>This is a report of unexplained anemia that persisted for 4 months in an adolescent renal transplant patient receiving immunosuppression that included prednisone, tacrolimus, and mycophenolate mofetil. This patient required monthly blood transfusions for fatigue, palpitations, and hematocrit levels between 15% and 17%. In addition, his posttransplant course was notable for the development of insulin-dependent diabetes mellitus. While receiving low-dose prednisone, he was switched from tacrolimus to cyclosporin and tapered off insulin injections over the next 2 months. At 4.5 months post-transplantation, further diagnostic evaluation was suggestive of parvovirus B19 infection as the cause for our patient's chronic anemia. After testing negative for serum-specific parvovirus B19 IgM and IgG antibodies, parvovirus B19 infection was detected in blood by the polymerase chain reaction. Treatment with intravenous immunoglobulin (1 g/kg per day x 2 days) resulted in normalization of both his reticulocyte count and hematocrit within 6 weeks. At 4 months after receiving the immunoglobulin infusion, he has maintained a normal hematocrit level and stable renal function without requiring further blood transfusions.</description><subject>Adolescent</subject><subject>Anemia</subject><subject>Anemia - blood</subject><subject>Anemia - etiology</subject><subject>Biological and medical sciences</subject><subject>Blood transfusion</subject><subject>Blood transfusions</subject><subject>Chronic Disease</subject><subject>Chronic infection</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Hematocrit</subject><subject>Humans</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Immunoglobulins</subject><subject>Immunosuppression</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Infections</subject><subject>Insulin</subject><subject>Intravenous administration</subject><subject>Kidney Function Tests</subject><subject>Kidney transplantation</subject><subject>Kidney Transplantation - physiology</subject><subject>Kidney transplants</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mycophenolate mofetil</subject><subject>Mycophenolic acid</subject><subject>Parvoviridae Infections - blood</subject><subject>Parvovirus B19, Human</subject><subject>Parvoviruses</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Polymerase Chain Reaction</subject><subject>Prednisone</subject><subject>Renal function</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Tacrolimus</subject><subject>Transplants & implants</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp10U1rFTEUBuAglXqtLl0KoRV3Y08-JpMs24tfUHBjobvh3EyCqTPJNJkp9N-bay8FC64SeJ-8HHIIecfgEwPozguAVB1AC9yoF2TDpOANM_rmiGzACNaAZDevyOtSbgFAt1odk2PDQTDDN8Rtf-UUg6UY3RSQYqFIbZrmMVhcQoo0eTpjvk_3Ia-FXjJDQ_TO_s1CrHp2Q8Al147fYYjugS4ZY5lHjEt9uQQXlzfkpcexuLeH84Rcf_n8c_utufrx9fv24qqxUuilUbu2XrxAsJ3ZDU5LPfhBo9WKaYvotUHhnHdsp0BKzVAi504O0g9Gei5OyMfH3jmnu9WVpZ9CsW6ss7i0lr4zDJhp9_DsGbxNa451tp4rI7tW6FZVdfpfxblQVe5R84hsTqVk5_s5hwnzQ8-g32-o_2dD1b8_lK67yQ1P-rCSmn845Fgsjr5-pg3lidXxtG6l-ANaUZgO</recordid><startdate>19970601</startdate><enddate>19970601</enddate><creator>MATHIAS, R. 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S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-6b5c43f3a0c79bde848dfd8ac8618caaf89a3eefe1b604481a4a22e4d4fd94f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adolescent</topic><topic>Anemia</topic><topic>Anemia - blood</topic><topic>Anemia - etiology</topic><topic>Biological and medical sciences</topic><topic>Blood transfusion</topic><topic>Blood transfusions</topic><topic>Chronic Disease</topic><topic>Chronic infection</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Hematocrit</topic><topic>Humans</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin M</topic><topic>Immunoglobulins</topic><topic>Immunosuppression</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Infections</topic><topic>Insulin</topic><topic>Intravenous administration</topic><topic>Kidney Function Tests</topic><topic>Kidney transplantation</topic><topic>Kidney Transplantation - physiology</topic><topic>Kidney transplants</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mycophenolate mofetil</topic><topic>Mycophenolic acid</topic><topic>Parvoviridae Infections - blood</topic><topic>Parvovirus B19, Human</topic><topic>Parvoviruses</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Polymerase Chain Reaction</topic><topic>Prednisone</topic><topic>Renal function</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Tacrolimus</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MATHIAS, R. 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S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic anemia as a complication of parvovirus B19 infection in a pediatric kidney transplant patient</atitle><jtitle>Pediatric nephrology (Berlin, West)</jtitle><addtitle>Pediatr Nephrol</addtitle><date>1997-06-01</date><risdate>1997</risdate><volume>11</volume><issue>3</issue><spage>355</spage><epage>357</epage><pages>355-357</pages><issn>0931-041X</issn><eissn>1432-198X</eissn><coden>PENED3</coden><abstract>This is a report of unexplained anemia that persisted for 4 months in an adolescent renal transplant patient receiving immunosuppression that included prednisone, tacrolimus, and mycophenolate mofetil. This patient required monthly blood transfusions for fatigue, palpitations, and hematocrit levels between 15% and 17%. In addition, his posttransplant course was notable for the development of insulin-dependent diabetes mellitus. While receiving low-dose prednisone, he was switched from tacrolimus to cyclosporin and tapered off insulin injections over the next 2 months. At 4.5 months post-transplantation, further diagnostic evaluation was suggestive of parvovirus B19 infection as the cause for our patient's chronic anemia. After testing negative for serum-specific parvovirus B19 IgM and IgG antibodies, parvovirus B19 infection was detected in blood by the polymerase chain reaction. Treatment with intravenous immunoglobulin (1 g/kg per day x 2 days) resulted in normalization of both his reticulocyte count and hematocrit within 6 weeks. At 4 months after receiving the immunoglobulin infusion, he has maintained a normal hematocrit level and stable renal function without requiring further blood transfusions.</abstract><cop>Heidelberg</cop><pub>Springer</pub><pmid>9203192</pmid><doi>10.1007/s004670050296</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Adolescent Anemia Anemia - blood Anemia - etiology Biological and medical sciences Blood transfusion Blood transfusions Chronic Disease Chronic infection Diabetes mellitus (insulin dependent) Hematocrit Humans Immunoglobulin G Immunoglobulin M Immunoglobulins Immunosuppression Immunosuppressive Agents - adverse effects Immunosuppressive Agents - therapeutic use Infections Insulin Intravenous administration Kidney Function Tests Kidney transplantation Kidney Transplantation - physiology Kidney transplants Male Medical sciences Mycophenolate mofetil Mycophenolic acid Parvoviridae Infections - blood Parvovirus B19, Human Parvoviruses Patients Pediatrics Polymerase Chain Reaction Prednisone Renal function Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Tacrolimus Transplants & implants |
title | Chronic anemia as a complication of parvovirus B19 infection in a pediatric kidney transplant patient |
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