Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Journal of pediatric surgery 2011-04, Vol.46 (4), p.764-766
Main Authors: Schiller, Ofer, Ash, Shifra, Schonfeld, Tommy, Kadmon, Gili, Nahum, Elhanan, Yacobovich, Joanne, Tamary, Hannah, Davidovits, Miriam
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-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803
cites cdi_FETCH-LOGICAL-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803
container_end_page 766
container_issue 4
container_start_page 764
container_title Journal of pediatric surgery
container_volume 46
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_862604756</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022346811000509</els_id><sourcerecordid>862604756</sourcerecordid><originalsourceid>FETCH-LOGICAL-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803</originalsourceid><addsrcrecordid>eNqFUcFu1DAQtRCIbgu_UOXGKdtx4jgOBwSqaEGqBFLhbHntCThk42A7Rfv3nWi7HLggjzzW85s3mjeMXXLYcuDyatgOM7q0xB_bCjjfAgV0z9iGNzUvG6jb52wDUFVlLaQ6Y-cpDQAEA3_JziouOtk01YaZryHlMGM02T9gkX_GsN-F7O3paQ_r90TAvEQKU_ipMBPdvZny28KahEXEOcRMsCtGn1exJa7og8c_r9iL3owJXz_lC_b95uO360_l3Zfbz9cf7korlMplt-NOSdErOkJg7XopBeetlX2j2tp0sm1V24GyToGoK2VtY1DKlu-cUQrqC_bmqDvH8HvBlPXeJ4vjaCYMS9JKVhJE20hiyiPTxpBSxF7P0e9NPGgOenVXD_rkrl7d1UABHRVePrVYdnt0f8tOdhLh_ZGANCgNH3WyHieLzke0Wbvg_9_j3T8SdvRkvxl_4QHTEJY4kY2a61Rp0PfrjtcVc07rbUjgEUWBpUc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>862604756</pqid></control><display><type>article</type><title>Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review</title><source>ScienceDirect Freedom Collection</source><creator>Schiller, Ofer ; Ash, Shifra ; Schonfeld, Tommy ; Kadmon, Gili ; Nahum, Elhanan ; Yacobovich, Joanne ; Tamary, Hannah ; Davidovits, Miriam</creator><creatorcontrib>Schiller, Ofer ; Ash, Shifra ; Schonfeld, Tommy ; Kadmon, Gili ; Nahum, Elhanan ; Yacobovich, Joanne ; Tamary, Hannah ; Davidovits, Miriam</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 0022-3468
ispartof Journal of pediatric surgery, 2011-04, Vol.46 (4), p.764-766
issn 0022-3468
1531-5037
language eng
recordid cdi_proquest_miscellaneous_862604756
source ScienceDirect Freedom Collection
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T23%3A31%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Postoperative%20thrombotic%20thrombocytopenic%20purpura%20in%20an%20infant:%20case%20report%20and%20literature%20review&rft.jtitle=Journal%20of%20pediatric%20surgery&rft.au=Schiller,%20Ofer&rft.date=2011-04-01&rft.volume=46&rft.issue=4&rft.spage=764&rft.epage=766&rft.pages=764-766&rft.issn=0022-3468&rft.eissn=1531-5037&rft_id=info:doi/10.1016/j.jpedsurg.2011.01.009&rft_dat=%3Cproquest_cross%3E862604756%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c488t-9b1d864f8f8f44e3df664117c6f5873a967787908cd804328cc5ae6671bda8803%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=862604756&rft_id=info:pmid/21496552&rfr_iscdi=true