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Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review
Abstract Thrombotic thrombocytopenic purpura is caused by an imbalance of von Willebrand factor and its cleaving protease, which leads to the formation of microthrombi in end-organs. It rarely occurs in the pediatric population. Plasma exchange can significantly reduce mortality and morbidity. We pr...
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Published in: | Journal of pediatric surgery 2011-04, Vol.46 (4), p.764-766 |
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container_title | Journal of pediatric surgery |
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creator | Schiller, Ofer Ash, Shifra Schonfeld, Tommy Kadmon, Gili Nahum, Elhanan Yacobovich, Joanne Tamary, Hannah Davidovits, Miriam |
description | Abstract Thrombotic thrombocytopenic purpura is caused by an imbalance of von Willebrand factor and its cleaving protease, which leads to the formation of microthrombi in end-organs. It rarely occurs in the pediatric population. Plasma exchange can significantly reduce mortality and morbidity. We present a 14-month-old infant in whom clinical and laboratory abnormalities compatible with thrombotic thrombocytopenic purpura were noted several days after resection of a large pelvic tumor. Treatment with double volume plasma exchange on postoperative day 5 led to complete resolution of the renal failure, thrombocytopenia, anemia, and neurological manifestations. ADAMTS13 inhibitors were negative and no mutations were found in factor H, factor I, membrane cofactor protein, and thrombomodulin to account for genetic predisposition to thrombotic thrombocytopenic purpura or atypical hemolytic uremic syndrome. Postoperative anemia, thrombocytopenia, fever, and neurological deficits in children should raise the suspicion of thrombotic thrombocytopenic purpura. Early diagnosis is important because the disorder is readily and efficiently treated with plasma exchange. |
doi_str_mv | 10.1016/j.jpedsurg.2011.01.009 |
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It rarely occurs in the pediatric population. Plasma exchange can significantly reduce mortality and morbidity. We present a 14-month-old infant in whom clinical and laboratory abnormalities compatible with thrombotic thrombocytopenic purpura were noted several days after resection of a large pelvic tumor. Treatment with double volume plasma exchange on postoperative day 5 led to complete resolution of the renal failure, thrombocytopenia, anemia, and neurological manifestations. ADAMTS13 inhibitors were negative and no mutations were found in factor H, factor I, membrane cofactor protein, and thrombomodulin to account for genetic predisposition to thrombotic thrombocytopenic purpura or atypical hemolytic uremic syndrome. Postoperative anemia, thrombocytopenia, fever, and neurological deficits in children should raise the suspicion of thrombotic thrombocytopenic purpura. Early diagnosis is important because the disorder is readily and efficiently treated with plasma exchange.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/j.jpedsurg.2011.01.009</identifier><identifier>PMID: 21496552</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Endodermal Sinus Tumor - surgery ; Female ; Hemolytic anemia ; Hemolytic uremic syndrome ; Humans ; Infant ; Laparotomy - adverse effects ; Pediatrics ; Pelvic Neoplasms - surgery ; Plasma Exchange - methods ; Plasmapheresis - methods ; Postoperative ; Postoperative Complications ; Purpura, Thrombotic Thrombocytopenic - blood ; Purpura, Thrombotic Thrombocytopenic - etiology ; Purpura, Thrombotic Thrombocytopenic - therapy ; Surgery ; Thrombotic microangiopathy ; Thrombotic thrombocytopenic purpura ; von Willebrand Factor - metabolism</subject><ispartof>Journal of pediatric surgery, 2011-04, Vol.46 (4), p.764-766</ispartof><rights>Elsevier Inc.</rights><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803</citedby><cites>FETCH-LOGICAL-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21496552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schiller, Ofer</creatorcontrib><creatorcontrib>Ash, Shifra</creatorcontrib><creatorcontrib>Schonfeld, Tommy</creatorcontrib><creatorcontrib>Kadmon, Gili</creatorcontrib><creatorcontrib>Nahum, Elhanan</creatorcontrib><creatorcontrib>Yacobovich, Joanne</creatorcontrib><creatorcontrib>Tamary, Hannah</creatorcontrib><creatorcontrib>Davidovits, Miriam</creatorcontrib><title>Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Abstract Thrombotic thrombocytopenic purpura is caused by an imbalance of von Willebrand factor and its cleaving protease, which leads to the formation of microthrombi in end-organs. It rarely occurs in the pediatric population. Plasma exchange can significantly reduce mortality and morbidity. We present a 14-month-old infant in whom clinical and laboratory abnormalities compatible with thrombotic thrombocytopenic purpura were noted several days after resection of a large pelvic tumor. Treatment with double volume plasma exchange on postoperative day 5 led to complete resolution of the renal failure, thrombocytopenia, anemia, and neurological manifestations. ADAMTS13 inhibitors were negative and no mutations were found in factor H, factor I, membrane cofactor protein, and thrombomodulin to account for genetic predisposition to thrombotic thrombocytopenic purpura or atypical hemolytic uremic syndrome. Postoperative anemia, thrombocytopenia, fever, and neurological deficits in children should raise the suspicion of thrombotic thrombocytopenic purpura. Early diagnosis is important because the disorder is readily and efficiently treated with plasma exchange.</description><subject>Endodermal Sinus Tumor - surgery</subject><subject>Female</subject><subject>Hemolytic anemia</subject><subject>Hemolytic uremic syndrome</subject><subject>Humans</subject><subject>Infant</subject><subject>Laparotomy - adverse effects</subject><subject>Pediatrics</subject><subject>Pelvic Neoplasms - surgery</subject><subject>Plasma Exchange - methods</subject><subject>Plasmapheresis - methods</subject><subject>Postoperative</subject><subject>Postoperative Complications</subject><subject>Purpura, Thrombotic Thrombocytopenic - blood</subject><subject>Purpura, Thrombotic Thrombocytopenic - etiology</subject><subject>Purpura, Thrombotic Thrombocytopenic - therapy</subject><subject>Surgery</subject><subject>Thrombotic microangiopathy</subject><subject>Thrombotic thrombocytopenic purpura</subject><subject>von Willebrand Factor - metabolism</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFUcFu1DAQtRCIbgu_UOXGKdtx4jgOBwSqaEGqBFLhbHntCThk42A7Rfv3nWi7HLggjzzW85s3mjeMXXLYcuDyatgOM7q0xB_bCjjfAgV0z9iGNzUvG6jb52wDUFVlLaQ6Y-cpDQAEA3_JziouOtk01YaZryHlMGM02T9gkX_GsN-F7O3paQ_r90TAvEQKU_ipMBPdvZny28KahEXEOcRMsCtGn1exJa7og8c_r9iL3owJXz_lC_b95uO360_l3Zfbz9cf7korlMplt-NOSdErOkJg7XopBeetlX2j2tp0sm1V24GyToGoK2VtY1DKlu-cUQrqC_bmqDvH8HvBlPXeJ4vjaCYMS9JKVhJE20hiyiPTxpBSxF7P0e9NPGgOenVXD_rkrl7d1UABHRVePrVYdnt0f8tOdhLh_ZGANCgNH3WyHieLzke0Wbvg_9_j3T8SdvRkvxl_4QHTEJY4kY2a61Rp0PfrjtcVc07rbUjgEUWBpUc</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>Schiller, Ofer</creator><creator>Ash, Shifra</creator><creator>Schonfeld, Tommy</creator><creator>Kadmon, Gili</creator><creator>Nahum, Elhanan</creator><creator>Yacobovich, Joanne</creator><creator>Tamary, Hannah</creator><creator>Davidovits, Miriam</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20110401</creationdate><title>Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review</title><author>Schiller, Ofer ; Ash, Shifra ; Schonfeld, Tommy ; Kadmon, Gili ; Nahum, Elhanan ; Yacobovich, Joanne ; Tamary, Hannah ; Davidovits, Miriam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Endodermal Sinus Tumor - surgery</topic><topic>Female</topic><topic>Hemolytic anemia</topic><topic>Hemolytic uremic syndrome</topic><topic>Humans</topic><topic>Infant</topic><topic>Laparotomy - adverse effects</topic><topic>Pediatrics</topic><topic>Pelvic Neoplasms - surgery</topic><topic>Plasma Exchange - methods</topic><topic>Plasmapheresis - methods</topic><topic>Postoperative</topic><topic>Postoperative Complications</topic><topic>Purpura, Thrombotic Thrombocytopenic - blood</topic><topic>Purpura, Thrombotic Thrombocytopenic - etiology</topic><topic>Purpura, Thrombotic Thrombocytopenic - therapy</topic><topic>Surgery</topic><topic>Thrombotic microangiopathy</topic><topic>Thrombotic thrombocytopenic purpura</topic><topic>von Willebrand Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schiller, Ofer</creatorcontrib><creatorcontrib>Ash, Shifra</creatorcontrib><creatorcontrib>Schonfeld, Tommy</creatorcontrib><creatorcontrib>Kadmon, Gili</creatorcontrib><creatorcontrib>Nahum, Elhanan</creatorcontrib><creatorcontrib>Yacobovich, Joanne</creatorcontrib><creatorcontrib>Tamary, Hannah</creatorcontrib><creatorcontrib>Davidovits, Miriam</creatorcontrib><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 pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schiller, Ofer</au><au>Ash, Shifra</au><au>Schonfeld, Tommy</au><au>Kadmon, Gili</au><au>Nahum, Elhanan</au><au>Yacobovich, Joanne</au><au>Tamary, Hannah</au><au>Davidovits, Miriam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>46</volume><issue>4</issue><spage>764</spage><epage>766</epage><pages>764-766</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><abstract>Abstract Thrombotic thrombocytopenic purpura is caused by an imbalance of von Willebrand factor and its cleaving protease, which leads to the formation of microthrombi in end-organs. It rarely occurs in the pediatric population. Plasma exchange can significantly reduce mortality and morbidity. We present a 14-month-old infant in whom clinical and laboratory abnormalities compatible with thrombotic thrombocytopenic purpura were noted several days after resection of a large pelvic tumor. Treatment with double volume plasma exchange on postoperative day 5 led to complete resolution of the renal failure, thrombocytopenia, anemia, and neurological manifestations. ADAMTS13 inhibitors were negative and no mutations were found in factor H, factor I, membrane cofactor protein, and thrombomodulin to account for genetic predisposition to thrombotic thrombocytopenic purpura or atypical hemolytic uremic syndrome. Postoperative anemia, thrombocytopenia, fever, and neurological deficits in children should raise the suspicion of thrombotic thrombocytopenic purpura. Early diagnosis is important because the disorder is readily and efficiently treated with plasma exchange.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21496552</pmid><doi>10.1016/j.jpedsurg.2011.01.009</doi><tpages>3</tpages></addata></record> |
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subjects | Endodermal Sinus Tumor - surgery Female Hemolytic anemia Hemolytic uremic syndrome Humans Infant Laparotomy - adverse effects Pediatrics Pelvic Neoplasms - surgery Plasma Exchange - methods Plasmapheresis - methods Postoperative Postoperative Complications Purpura, Thrombotic Thrombocytopenic - blood Purpura, Thrombotic Thrombocytopenic - etiology Purpura, Thrombotic Thrombocytopenic - therapy Surgery Thrombotic microangiopathy Thrombotic thrombocytopenic purpura von Willebrand Factor - metabolism |
title | Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review |
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