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Articles Published Processes
4/30/2022 5:08:22 AM | Browse: 512 | Download: 1267
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Received |
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2021-08-11 05:07 |
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Peer-Review Started |
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2021-08-11 05:10 |
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First Decision by Editorial Office Director |
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2021-09-02 00:59 |
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Return for Revision |
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2021-09-02 00:59 |
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Revised |
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2021-09-17 07:18 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2022-03-11 06:06 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2022-03-16 16:21 |
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Articles in Press |
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2022-03-16 16:21 |
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Edit the Manuscript by Language Editor |
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2022-02-27 15:07 |
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Typeset the Manuscript |
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2022-04-17 13:20 |
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Publish the Manuscript Online |
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2022-04-30 05:08 |
| ISSN |
2307-8960 (online) |
| Open Access |
This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Hematology |
| Manuscript Type |
Case Report |
| Article Title |
Primary myelofibrosis with thrombophilia as first symptom combined with thalassemia and Gilbert syndrome: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Guzailinuer Wufuer, Kaisaer Wufuer, Tu Ba, Tao Cui, Ling Tao, Ling Fu, Ming Mao and Ming-Hui Duan |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Ming-Hui Duan, MD, Doctor, Doctor, Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Shuaifuyuan, Dongcheng District, Beijing 100730, China. mhduan@sina.com |
| Key Words |
Thrombophilia; Prefibrotic myelofibrosis; Negative family thrombosis history; Case report |
| Core Tip |
Thrombophilia is genetic or acquired defect, or there are acquired risk factors and a high thromboembolic tendency. Hereditary antithrombin (AT) deficiency is a genetic defect caused by a mutation in the AT coding gene SERPINCI1, which is one of the major risk factors for hereditary thrombophilia. We report a case of thrombotic disorder with hereditary AT deficiency, in which genetic tests revealed a heterozygous SERPINC1 mutation, and a JAK2V617-positive myeloproliferative neoplasm was a potential acquisition factor for venous thrombosis. At the same time, this patient was genetically confirmed to have both UGT1A1 and β-thalassemia gene mutations. In clinical work, under the premise of clear thrombophilia, comprehensive screening of relevant occult factors is necessary. |
| Publish Date |
2022-04-30 05:08 |
| Citation |
Wufuer G, Wufuer K, Ba T, Cui T, Tao L, Fu L, Mao M, Duan MH. Primary myelofibrosis with thrombophilia as first symptom combined with thalassemia and Gilbert syndrome: A case report. World J Clin Cases 2022; 10(13): 4161-4170 |
| URL |
https://www.wjgnet.com/2307-8960/full/v10/i13/4161.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v10.i13.4161 |
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