Two pregnant women with immune‐mediated thrombotic thrombocytopenic purpura: A case report
Thrombotic thrombocytopenic purpura (TTP) during pregnancy is life‐threatening. We encountered two pregnant women with immune‐mediated TTP (iTTP). A 40‐year‐old primigravida woman was referred at 19 gestational weeks (GWs) owing to iTTP. She received plasma exchange (PE) and steroid therapies and de...
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Veröffentlicht in: | The journal of obstetrics and gynaecology research 2023-12, Vol.49 (12), p.2969-2974 |
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container_title | The journal of obstetrics and gynaecology research |
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creator | Uchida, Akiko Tanimura, Kenji Sasagawa, Yuki Yamada, Hirotaka Katayama, Yoshio Matsumoto, Masanori |
description | Thrombotic thrombocytopenic purpura (TTP) during pregnancy is life‐threatening. We encountered two pregnant women with immune‐mediated TTP (iTTP). A 40‐year‐old primigravida woman was referred at 19 gestational weeks (GWs) owing to iTTP. She received plasma exchange (PE) and steroid therapies and delivered a live infant at 27 GWs by cesarean delivery. A 29‐year‐old primigravida woman was referred owing to intrauterine fetal death and thrombocytopenia at 20 GWs. She was diagnosed with iTTP and received PE therapy. She required additional PE and steroid therapies owing to relapse. Before her second pregnancy, she received prednisolone and hydroxychloroquine according to the therapy for systemic lupus erythematosus (SLE). She had induced labor at 37 GWs owing to decrease plasma level of a disintegrin‐like and metalloproteinase with thrombospondin type 1 motif 13 (ADAMTS13) activity. Close monitoring of plasma ADAMTS13 activity level and treatments for underlying SLE may prevent iTTP relapse and lead to a good prognosis. |
doi_str_mv | 10.1111/jog.15793 |
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We encountered two pregnant women with immune‐mediated TTP (iTTP). A 40‐year‐old primigravida woman was referred at 19 gestational weeks (GWs) owing to iTTP. She received plasma exchange (PE) and steroid therapies and delivered a live infant at 27 GWs by cesarean delivery. A 29‐year‐old primigravida woman was referred owing to intrauterine fetal death and thrombocytopenia at 20 GWs. She was diagnosed with iTTP and received PE therapy. She required additional PE and steroid therapies owing to relapse. Before her second pregnancy, she received prednisolone and hydroxychloroquine according to the therapy for systemic lupus erythematosus (SLE). She had induced labor at 37 GWs owing to decrease plasma level of a disintegrin‐like and metalloproteinase with thrombospondin type 1 motif 13 (ADAMTS13) activity. Close monitoring of plasma ADAMTS13 activity level and treatments for underlying SLE may prevent iTTP relapse and lead to a good prognosis.</description><identifier>ISSN: 1341-8076</identifier><identifier>EISSN: 1447-0756</identifier><identifier>DOI: 10.1111/jog.15793</identifier><language>eng</language><publisher>Kyoto, Japan: John Wiley & Sons Australia, Ltd</publisher><subject>ADAMTS13 ; Case reports ; Cesarean section ; Fetuses ; Hydroxychloroquine ; immune‐mediated thrombotic thrombocytopenic purpura ; plasma exchange ; Prednisolone ; Pregnancy ; Pregnancy complications ; steroid ; Systemic lupus erythematosus ; Thrombocytopenia ; Thrombocytopenic purpura ; Thrombospondin ; Thrombotic thrombocytopenic purpura</subject><ispartof>The journal of obstetrics and gynaecology research, 2023-12, Vol.49 (12), p.2969-2974</ispartof><rights>2023 Japan Society of Obstetrics and Gynecology.</rights><rights>2023 Japan Society of Obstetrics and Gynecology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3363-86e9ec00c01ee04f4c74117b3c867ed601389aeb2f56a4d62c0300ba2a6e205d3</cites><orcidid>0000-0003-1435-120X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjog.15793$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjog.15793$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids></links><search><creatorcontrib>Uchida, Akiko</creatorcontrib><creatorcontrib>Tanimura, Kenji</creatorcontrib><creatorcontrib>Sasagawa, Yuki</creatorcontrib><creatorcontrib>Yamada, Hirotaka</creatorcontrib><creatorcontrib>Katayama, Yoshio</creatorcontrib><creatorcontrib>Matsumoto, Masanori</creatorcontrib><title>Two pregnant women with immune‐mediated thrombotic thrombocytopenic purpura: A case report</title><title>The journal of obstetrics and gynaecology research</title><description>Thrombotic thrombocytopenic purpura (TTP) during pregnancy is life‐threatening. We encountered two pregnant women with immune‐mediated TTP (iTTP). A 40‐year‐old primigravida woman was referred at 19 gestational weeks (GWs) owing to iTTP. She received plasma exchange (PE) and steroid therapies and delivered a live infant at 27 GWs by cesarean delivery. A 29‐year‐old primigravida woman was referred owing to intrauterine fetal death and thrombocytopenia at 20 GWs. She was diagnosed with iTTP and received PE therapy. She required additional PE and steroid therapies owing to relapse. Before her second pregnancy, she received prednisolone and hydroxychloroquine according to the therapy for systemic lupus erythematosus (SLE). She had induced labor at 37 GWs owing to decrease plasma level of a disintegrin‐like and metalloproteinase with thrombospondin type 1 motif 13 (ADAMTS13) activity. Close monitoring of plasma ADAMTS13 activity level and treatments for underlying SLE may prevent iTTP relapse and lead to a good prognosis.</description><subject>ADAMTS13</subject><subject>Case reports</subject><subject>Cesarean section</subject><subject>Fetuses</subject><subject>Hydroxychloroquine</subject><subject>immune‐mediated thrombotic thrombocytopenic purpura</subject><subject>plasma exchange</subject><subject>Prednisolone</subject><subject>Pregnancy</subject><subject>Pregnancy complications</subject><subject>steroid</subject><subject>Systemic lupus erythematosus</subject><subject>Thrombocytopenia</subject><subject>Thrombocytopenic purpura</subject><subject>Thrombospondin</subject><subject>Thrombotic thrombocytopenic purpura</subject><issn>1341-8076</issn><issn>1447-0756</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kMFKw0AQhhdRsFYPvsGCJw9pZ7PJbuKtFK1KoZd6E8JmM2lTmmzcbCi9-Qg-o0_iavToMDA_w_fPwE_INYMJ8zXdmc2ExTLlJ2TEokgGIGNx6jWPWJCAFOfkout2AEymLBmR1_XB0NbiplGNowdTY0MPldvSqq77Bj_fP2osKuWwoG5rTZ0bV-k_qY_OtNj4Rdtb3-qOzqhWHVKLrbHukpyVat_h1e8ck5eH-_X8MViuFk_z2TLQnAseJAJT1AAaGCJEZaRlxJjMuU6ExEIA40mqMA_LWKioEKEGDpCrUAkMIS74mNwMd1tr3nrsXLYzvW38yyxMUsHTNOTSU7cDpa3pOotl1tqqVvaYMci-w_OuTfYTnmenA3uo9nj8H8yeV4vB8QWK9XKv</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Uchida, Akiko</creator><creator>Tanimura, Kenji</creator><creator>Sasagawa, Yuki</creator><creator>Yamada, Hirotaka</creator><creator>Katayama, Yoshio</creator><creator>Matsumoto, Masanori</creator><general>John Wiley & Sons Australia, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0003-1435-120X</orcidid></search><sort><creationdate>202312</creationdate><title>Two pregnant women with immune‐mediated thrombotic thrombocytopenic purpura: A case report</title><author>Uchida, Akiko ; Tanimura, Kenji ; Sasagawa, Yuki ; Yamada, Hirotaka ; Katayama, Yoshio ; Matsumoto, Masanori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3363-86e9ec00c01ee04f4c74117b3c867ed601389aeb2f56a4d62c0300ba2a6e205d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>ADAMTS13</topic><topic>Case reports</topic><topic>Cesarean section</topic><topic>Fetuses</topic><topic>Hydroxychloroquine</topic><topic>immune‐mediated thrombotic thrombocytopenic purpura</topic><topic>plasma exchange</topic><topic>Prednisolone</topic><topic>Pregnancy</topic><topic>Pregnancy complications</topic><topic>steroid</topic><topic>Systemic lupus erythematosus</topic><topic>Thrombocytopenia</topic><topic>Thrombocytopenic purpura</topic><topic>Thrombospondin</topic><topic>Thrombotic thrombocytopenic purpura</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uchida, Akiko</creatorcontrib><creatorcontrib>Tanimura, Kenji</creatorcontrib><creatorcontrib>Sasagawa, Yuki</creatorcontrib><creatorcontrib>Yamada, Hirotaka</creatorcontrib><creatorcontrib>Katayama, Yoshio</creatorcontrib><creatorcontrib>Matsumoto, Masanori</creatorcontrib><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>The journal of obstetrics and gynaecology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uchida, Akiko</au><au>Tanimura, Kenji</au><au>Sasagawa, Yuki</au><au>Yamada, Hirotaka</au><au>Katayama, Yoshio</au><au>Matsumoto, Masanori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two pregnant women with immune‐mediated thrombotic thrombocytopenic purpura: A case report</atitle><jtitle>The journal of obstetrics and gynaecology research</jtitle><date>2023-12</date><risdate>2023</risdate><volume>49</volume><issue>12</issue><spage>2969</spage><epage>2974</epage><pages>2969-2974</pages><issn>1341-8076</issn><eissn>1447-0756</eissn><abstract>Thrombotic thrombocytopenic purpura (TTP) during pregnancy is life‐threatening. We encountered two pregnant women with immune‐mediated TTP (iTTP). A 40‐year‐old primigravida woman was referred at 19 gestational weeks (GWs) owing to iTTP. She received plasma exchange (PE) and steroid therapies and delivered a live infant at 27 GWs by cesarean delivery. A 29‐year‐old primigravida woman was referred owing to intrauterine fetal death and thrombocytopenia at 20 GWs. She was diagnosed with iTTP and received PE therapy. She required additional PE and steroid therapies owing to relapse. Before her second pregnancy, she received prednisolone and hydroxychloroquine according to the therapy for systemic lupus erythematosus (SLE). She had induced labor at 37 GWs owing to decrease plasma level of a disintegrin‐like and metalloproteinase with thrombospondin type 1 motif 13 (ADAMTS13) activity. Close monitoring of plasma ADAMTS13 activity level and treatments for underlying SLE may prevent iTTP relapse and lead to a good prognosis.</abstract><cop>Kyoto, Japan</cop><pub>John Wiley & Sons Australia, Ltd</pub><doi>10.1111/jog.15793</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-1435-120X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ADAMTS13 Case reports Cesarean section Fetuses Hydroxychloroquine immune‐mediated thrombotic thrombocytopenic purpura plasma exchange Prednisolone Pregnancy Pregnancy complications steroid Systemic lupus erythematosus Thrombocytopenia Thrombocytopenic purpura Thrombospondin Thrombotic thrombocytopenic purpura |
title | Two pregnant women with immune‐mediated thrombotic thrombocytopenic purpura: A case report |
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