Loading…

Autoimmune pancytopenia after liver transplantation: A case report

Autoimmune hemolytic anemia (AIHA), immune thrombocytopenia (ITP), and autoimmune neutropenia (AIN) are reported in the literature after liver, intestinal, heart, pancreas, and kidney transplants. We report a case of autoimmune pancytopenia (AIHA, AIN and ITP) 9 years after liver transplantation wit...

Full description

Saved in:
Bibliographic Details
Published in:Transfusion and apheresis science 2021-08, Vol.60 (4), p.103136-103136, Article 103136
Main Authors: Barros, Melca Maria Oliveira, Ayoub, Fauze Lutfe, Lemos, Giovanna, Brasileiro, Kelly Cristina, da Silva Icibaci, Priscilla Brito, Moritz, Elyse, Martins, Juliana Oliveira, Bub, Carolina Bonet, Chiba, Akemi Kuroda, Bordin, Jose Orlando
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-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3
cites cdi_FETCH-LOGICAL-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3
container_end_page 103136
container_issue 4
container_start_page 103136
container_title Transfusion and apheresis science
container_volume 60
creator Barros, Melca Maria Oliveira
Ayoub, Fauze Lutfe
Lemos, Giovanna
Brasileiro, Kelly Cristina
da Silva Icibaci, Priscilla Brito
Moritz, Elyse
Martins, Juliana Oliveira
Bub, Carolina Bonet
Chiba, Akemi Kuroda
Bordin, Jose Orlando
description Autoimmune hemolytic anemia (AIHA), immune thrombocytopenia (ITP), and autoimmune neutropenia (AIN) are reported in the literature after liver, intestinal, heart, pancreas, and kidney transplants. We report a case of autoimmune pancytopenia (AIHA, AIN and ITP) 9 years after liver transplantation with confirmed erythrocyte and neutrophil auto-antibodies. A 49 years old man was admitted to our hospital presented with dysentery and fever, with history of liver transplantation in 2008. Laboratory evaluation demonstrated hemoglobin: 7.2 g/dL, granulocytes: 0.10 × 109/L and platelets: 15 × 109/mm³; indirect bilirubin: 3.62 mg/dL; lactate dehydrogenase: 603 U/L. Direct antiglobulin test revealed a monospecific anti-IgG plus C3 and the acid eluate was reactive to all panel red cells, consistent with an AIHA. Granulocyte immunofluorescence test (GIFT) and agglutination test (GAT) were reactive for granulocytes. Test with Luminex technology for human neutrophil antigen (HNA) antibody detection was strong reactive with beads expressing HNA-1a, -1b, -1c, -2, -4a and -5a antigens. HNA genotyping revealed the presence of the corresponding antigens, confirming the autoantibodies. Test with Luminex technology for human leucocyte antigen (HLA) antibody detection was negative. Monoclonal antibody immobilization of platelet antigens (MAIPA) assay was negative. Viral causes were excluded. The condition was compatible with clinical onset of autoimmune pancytopenia. Prednisone was administered at an initial dose of 1 mg/kg/day and immunosuppressive therapy was adjusted. This treatment resulted in rapid resolution of pancytopenia. Combined autoimmune pancytopenia (AIHA, AIN and ITP) is a rare condition that may occur after liver transplantation. Early recognition of this phenomenon permits appropriate treatment.
doi_str_mv 10.1016/j.transci.2021.103136
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2518725164</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1473050221001026</els_id><sourcerecordid>2518725164</sourcerecordid><originalsourceid>FETCH-LOGICAL-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3</originalsourceid><addsrcrecordid>eNqFkMtKAzEUhoMotlYfQZmlm6m5dJKMG6nFGxTc6DrE5ARSOheTTMG3N3WqWzfnEv5z_pwPoUuC5wQTfrOZp6DbaPycYkryGyOMH6EpkUKWhEt2nOuFYCWuMJ2gsxg3GBNBan6KJozJusICT9H9ckidb5qhhaLXrflKXQ-t14V2CUKx9bscf5z6rW6TTr5rb4tlYXSEIkDfhXSOTpzeRrg45Bl6f3x4Wz2X69enl9VyXRrGq1QuZC2xrR1x2HFtLatqqB04QZnRIGpBqXbCElHx3BtOrJSOWikWTlNeWTZD1-PePnSfA8SkGh8NbPO_oBuiolW-PQe-yNJqlJrQxRjAqT74RocvRbDa41MbdcCn9vjUiC_PXR0sho8G7N_UL68suBsFkA_deQgqr4DWgPUBTFK28_9YfAMIpIRK</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2518725164</pqid></control><display><type>article</type><title>Autoimmune pancytopenia after liver transplantation: A case report</title><source>ScienceDirect Freedom Collection</source><creator>Barros, Melca Maria Oliveira ; Ayoub, Fauze Lutfe ; Lemos, Giovanna ; Brasileiro, Kelly Cristina ; da Silva Icibaci, Priscilla Brito ; Moritz, Elyse ; Martins, Juliana Oliveira ; Bub, Carolina Bonet ; Chiba, Akemi Kuroda ; Bordin, Jose Orlando</creator><creatorcontrib>Barros, Melca Maria Oliveira ; Ayoub, Fauze Lutfe ; Lemos, Giovanna ; Brasileiro, Kelly Cristina ; da Silva Icibaci, Priscilla Brito ; Moritz, Elyse ; Martins, Juliana Oliveira ; Bub, Carolina Bonet ; Chiba, Akemi Kuroda ; Bordin, Jose Orlando</creatorcontrib><description>Autoimmune hemolytic anemia (AIHA), immune thrombocytopenia (ITP), and autoimmune neutropenia (AIN) are reported in the literature after liver, intestinal, heart, pancreas, and kidney transplants. We report a case of autoimmune pancytopenia (AIHA, AIN and ITP) 9 years after liver transplantation with confirmed erythrocyte and neutrophil auto-antibodies. A 49 years old man was admitted to our hospital presented with dysentery and fever, with history of liver transplantation in 2008. Laboratory evaluation demonstrated hemoglobin: 7.2 g/dL, granulocytes: 0.10 × 109/L and platelets: 15 × 109/mm³; indirect bilirubin: 3.62 mg/dL; lactate dehydrogenase: 603 U/L. Direct antiglobulin test revealed a monospecific anti-IgG plus C3 and the acid eluate was reactive to all panel red cells, consistent with an AIHA. Granulocyte immunofluorescence test (GIFT) and agglutination test (GAT) were reactive for granulocytes. Test with Luminex technology for human neutrophil antigen (HNA) antibody detection was strong reactive with beads expressing HNA-1a, -1b, -1c, -2, -4a and -5a antigens. HNA genotyping revealed the presence of the corresponding antigens, confirming the autoantibodies. Test with Luminex technology for human leucocyte antigen (HLA) antibody detection was negative. Monoclonal antibody immobilization of platelet antigens (MAIPA) assay was negative. Viral causes were excluded. The condition was compatible with clinical onset of autoimmune pancytopenia. Prednisone was administered at an initial dose of 1 mg/kg/day and immunosuppressive therapy was adjusted. This treatment resulted in rapid resolution of pancytopenia. Combined autoimmune pancytopenia (AIHA, AIN and ITP) is a rare condition that may occur after liver transplantation. Early recognition of this phenomenon permits appropriate treatment.</description><identifier>ISSN: 1473-0502</identifier><identifier>EISSN: 1878-1683</identifier><identifier>DOI: 10.1016/j.transci.2021.103136</identifier><identifier>PMID: 33895070</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Autoantibodies - blood ; Autoimmune Diseases - blood ; Autoimmune Diseases - etiology ; Autoimmune Diseases - therapy ; Autoimmune hemolytic anemia (AIHA) ; Autoimmune neutropenia (AIN) ; Case report ; GIFT ; Humans ; Immune thrombocytopenia (ITP) ; Immunosuppression Therapy ; Liver Transplantation ; MAIPA ; Male ; Middle Aged ; Pancytopenia - blood ; Pancytopenia - etiology ; Pancytopenia - therapy ; Prednisolone - administration &amp; dosage</subject><ispartof>Transfusion and apheresis science, 2021-08, Vol.60 (4), p.103136-103136, Article 103136</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3</citedby><cites>FETCH-LOGICAL-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3</cites><orcidid>0000-0002-5417-8336 ; 0000-0002-6625-6071 ; 0000-0001-5103-4970</orcidid></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/33895070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barros, Melca Maria Oliveira</creatorcontrib><creatorcontrib>Ayoub, Fauze Lutfe</creatorcontrib><creatorcontrib>Lemos, Giovanna</creatorcontrib><creatorcontrib>Brasileiro, Kelly Cristina</creatorcontrib><creatorcontrib>da Silva Icibaci, Priscilla Brito</creatorcontrib><creatorcontrib>Moritz, Elyse</creatorcontrib><creatorcontrib>Martins, Juliana Oliveira</creatorcontrib><creatorcontrib>Bub, Carolina Bonet</creatorcontrib><creatorcontrib>Chiba, Akemi Kuroda</creatorcontrib><creatorcontrib>Bordin, Jose Orlando</creatorcontrib><title>Autoimmune pancytopenia after liver transplantation: A case report</title><title>Transfusion and apheresis science</title><addtitle>Transfus Apher Sci</addtitle><description>Autoimmune hemolytic anemia (AIHA), immune thrombocytopenia (ITP), and autoimmune neutropenia (AIN) are reported in the literature after liver, intestinal, heart, pancreas, and kidney transplants. We report a case of autoimmune pancytopenia (AIHA, AIN and ITP) 9 years after liver transplantation with confirmed erythrocyte and neutrophil auto-antibodies. A 49 years old man was admitted to our hospital presented with dysentery and fever, with history of liver transplantation in 2008. Laboratory evaluation demonstrated hemoglobin: 7.2 g/dL, granulocytes: 0.10 × 109/L and platelets: 15 × 109/mm³; indirect bilirubin: 3.62 mg/dL; lactate dehydrogenase: 603 U/L. Direct antiglobulin test revealed a monospecific anti-IgG plus C3 and the acid eluate was reactive to all panel red cells, consistent with an AIHA. Granulocyte immunofluorescence test (GIFT) and agglutination test (GAT) were reactive for granulocytes. Test with Luminex technology for human neutrophil antigen (HNA) antibody detection was strong reactive with beads expressing HNA-1a, -1b, -1c, -2, -4a and -5a antigens. HNA genotyping revealed the presence of the corresponding antigens, confirming the autoantibodies. Test with Luminex technology for human leucocyte antigen (HLA) antibody detection was negative. Monoclonal antibody immobilization of platelet antigens (MAIPA) assay was negative. Viral causes were excluded. The condition was compatible with clinical onset of autoimmune pancytopenia. Prednisone was administered at an initial dose of 1 mg/kg/day and immunosuppressive therapy was adjusted. This treatment resulted in rapid resolution of pancytopenia. Combined autoimmune pancytopenia (AIHA, AIN and ITP) is a rare condition that may occur after liver transplantation. Early recognition of this phenomenon permits appropriate treatment.</description><subject>Autoantibodies - blood</subject><subject>Autoimmune Diseases - blood</subject><subject>Autoimmune Diseases - etiology</subject><subject>Autoimmune Diseases - therapy</subject><subject>Autoimmune hemolytic anemia (AIHA)</subject><subject>Autoimmune neutropenia (AIN)</subject><subject>Case report</subject><subject>GIFT</subject><subject>Humans</subject><subject>Immune thrombocytopenia (ITP)</subject><subject>Immunosuppression Therapy</subject><subject>Liver Transplantation</subject><subject>MAIPA</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pancytopenia - blood</subject><subject>Pancytopenia - etiology</subject><subject>Pancytopenia - therapy</subject><subject>Prednisolone - administration &amp; dosage</subject><issn>1473-0502</issn><issn>1878-1683</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKAzEUhoMotlYfQZmlm6m5dJKMG6nFGxTc6DrE5ARSOheTTMG3N3WqWzfnEv5z_pwPoUuC5wQTfrOZp6DbaPycYkryGyOMH6EpkUKWhEt2nOuFYCWuMJ2gsxg3GBNBan6KJozJusICT9H9ckidb5qhhaLXrflKXQ-t14V2CUKx9bscf5z6rW6TTr5rb4tlYXSEIkDfhXSOTpzeRrg45Bl6f3x4Wz2X69enl9VyXRrGq1QuZC2xrR1x2HFtLatqqB04QZnRIGpBqXbCElHx3BtOrJSOWikWTlNeWTZD1-PePnSfA8SkGh8NbPO_oBuiolW-PQe-yNJqlJrQxRjAqT74RocvRbDa41MbdcCn9vjUiC_PXR0sho8G7N_UL68suBsFkA_deQgqr4DWgPUBTFK28_9YfAMIpIRK</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Barros, Melca Maria Oliveira</creator><creator>Ayoub, Fauze Lutfe</creator><creator>Lemos, Giovanna</creator><creator>Brasileiro, Kelly Cristina</creator><creator>da Silva Icibaci, Priscilla Brito</creator><creator>Moritz, Elyse</creator><creator>Martins, Juliana Oliveira</creator><creator>Bub, Carolina Bonet</creator><creator>Chiba, Akemi Kuroda</creator><creator>Bordin, Jose Orlando</creator><general>Elsevier Ltd</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><orcidid>https://orcid.org/0000-0002-5417-8336</orcidid><orcidid>https://orcid.org/0000-0002-6625-6071</orcidid><orcidid>https://orcid.org/0000-0001-5103-4970</orcidid></search><sort><creationdate>202108</creationdate><title>Autoimmune pancytopenia after liver transplantation: A case report</title><author>Barros, Melca Maria Oliveira ; Ayoub, Fauze Lutfe ; Lemos, Giovanna ; Brasileiro, Kelly Cristina ; da Silva Icibaci, Priscilla Brito ; Moritz, Elyse ; Martins, Juliana Oliveira ; Bub, Carolina Bonet ; Chiba, Akemi Kuroda ; Bordin, Jose Orlando</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Autoantibodies - blood</topic><topic>Autoimmune Diseases - blood</topic><topic>Autoimmune Diseases - etiology</topic><topic>Autoimmune Diseases - therapy</topic><topic>Autoimmune hemolytic anemia (AIHA)</topic><topic>Autoimmune neutropenia (AIN)</topic><topic>Case report</topic><topic>GIFT</topic><topic>Humans</topic><topic>Immune thrombocytopenia (ITP)</topic><topic>Immunosuppression Therapy</topic><topic>Liver Transplantation</topic><topic>MAIPA</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pancytopenia - blood</topic><topic>Pancytopenia - etiology</topic><topic>Pancytopenia - therapy</topic><topic>Prednisolone - administration &amp; dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barros, Melca Maria Oliveira</creatorcontrib><creatorcontrib>Ayoub, Fauze Lutfe</creatorcontrib><creatorcontrib>Lemos, Giovanna</creatorcontrib><creatorcontrib>Brasileiro, Kelly Cristina</creatorcontrib><creatorcontrib>da Silva Icibaci, Priscilla Brito</creatorcontrib><creatorcontrib>Moritz, Elyse</creatorcontrib><creatorcontrib>Martins, Juliana Oliveira</creatorcontrib><creatorcontrib>Bub, Carolina Bonet</creatorcontrib><creatorcontrib>Chiba, Akemi Kuroda</creatorcontrib><creatorcontrib>Bordin, Jose Orlando</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>Transfusion and apheresis science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barros, Melca Maria Oliveira</au><au>Ayoub, Fauze Lutfe</au><au>Lemos, Giovanna</au><au>Brasileiro, Kelly Cristina</au><au>da Silva Icibaci, Priscilla Brito</au><au>Moritz, Elyse</au><au>Martins, Juliana Oliveira</au><au>Bub, Carolina Bonet</au><au>Chiba, Akemi Kuroda</au><au>Bordin, Jose Orlando</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autoimmune pancytopenia after liver transplantation: A case report</atitle><jtitle>Transfusion and apheresis science</jtitle><addtitle>Transfus Apher Sci</addtitle><date>2021-08</date><risdate>2021</risdate><volume>60</volume><issue>4</issue><spage>103136</spage><epage>103136</epage><pages>103136-103136</pages><artnum>103136</artnum><issn>1473-0502</issn><eissn>1878-1683</eissn><abstract>Autoimmune hemolytic anemia (AIHA), immune thrombocytopenia (ITP), and autoimmune neutropenia (AIN) are reported in the literature after liver, intestinal, heart, pancreas, and kidney transplants. We report a case of autoimmune pancytopenia (AIHA, AIN and ITP) 9 years after liver transplantation with confirmed erythrocyte and neutrophil auto-antibodies. A 49 years old man was admitted to our hospital presented with dysentery and fever, with history of liver transplantation in 2008. Laboratory evaluation demonstrated hemoglobin: 7.2 g/dL, granulocytes: 0.10 × 109/L and platelets: 15 × 109/mm³; indirect bilirubin: 3.62 mg/dL; lactate dehydrogenase: 603 U/L. Direct antiglobulin test revealed a monospecific anti-IgG plus C3 and the acid eluate was reactive to all panel red cells, consistent with an AIHA. Granulocyte immunofluorescence test (GIFT) and agglutination test (GAT) were reactive for granulocytes. Test with Luminex technology for human neutrophil antigen (HNA) antibody detection was strong reactive with beads expressing HNA-1a, -1b, -1c, -2, -4a and -5a antigens. HNA genotyping revealed the presence of the corresponding antigens, confirming the autoantibodies. Test with Luminex technology for human leucocyte antigen (HLA) antibody detection was negative. Monoclonal antibody immobilization of platelet antigens (MAIPA) assay was negative. Viral causes were excluded. The condition was compatible with clinical onset of autoimmune pancytopenia. Prednisone was administered at an initial dose of 1 mg/kg/day and immunosuppressive therapy was adjusted. This treatment resulted in rapid resolution of pancytopenia. Combined autoimmune pancytopenia (AIHA, AIN and ITP) is a rare condition that may occur after liver transplantation. Early recognition of this phenomenon permits appropriate treatment.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>33895070</pmid><doi>10.1016/j.transci.2021.103136</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5417-8336</orcidid><orcidid>https://orcid.org/0000-0002-6625-6071</orcidid><orcidid>https://orcid.org/0000-0001-5103-4970</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1473-0502
ispartof Transfusion and apheresis science, 2021-08, Vol.60 (4), p.103136-103136, Article 103136
issn 1473-0502
1878-1683
language eng
recordid cdi_proquest_miscellaneous_2518725164
source ScienceDirect Freedom Collection
subjects Autoantibodies - blood
Autoimmune Diseases - blood
Autoimmune Diseases - etiology
Autoimmune Diseases - therapy
Autoimmune hemolytic anemia (AIHA)
Autoimmune neutropenia (AIN)
Case report
GIFT
Humans
Immune thrombocytopenia (ITP)
Immunosuppression Therapy
Liver Transplantation
MAIPA
Male
Middle Aged
Pancytopenia - blood
Pancytopenia - etiology
Pancytopenia - therapy
Prednisolone - administration & dosage
title Autoimmune pancytopenia after liver transplantation: A case report
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T05%3A05%3A21IST&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=Autoimmune%20pancytopenia%20after%20liver%20transplantation:%20A%20case%20report&rft.jtitle=Transfusion%20and%20apheresis%20science&rft.au=Barros,%20Melca%20Maria%20Oliveira&rft.date=2021-08&rft.volume=60&rft.issue=4&rft.spage=103136&rft.epage=103136&rft.pages=103136-103136&rft.artnum=103136&rft.issn=1473-0502&rft.eissn=1878-1683&rft_id=info:doi/10.1016/j.transci.2021.103136&rft_dat=%3Cproquest_cross%3E2518725164%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c365t-48980d9f1f0f6add359e9fef723cae79722af7d1756caec61d88f2d874fa265d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2518725164&rft_id=info:pmid/33895070&rfr_iscdi=true