Antithrombin deficiency with portal vein and superior mesenteric vein thrombosis-a case report

被引:1
|
作者
Saidin, Nur Ilyia Syazwani [1 ]
Jamallodin, Fatma Basyira [1 ]
Hassan, Mohd Nazri [1 ]
Iberahim, Salfarina [1 ]
Abdullah, Abdul Hanan [2 ]
Zahidin, Muhamad Aidil [1 ]
Zulkafli, Zefarina [1 ]
Noor, Noor Haslina Mohd [1 ]
机构
[1] Univ Sains Malaysia, Haematol Dept, Hlth Campus, Kubang Kerian 16150, Kelantan, Malaysia
[2] Univ Sains Malaysia, Dept Internal Med, Hlth Campus, Kubang Kerian 16150, Kelantan, Malaysia
来源
BIOMEDICAL RESEARCH AND THERAPY | 2024年 / 11卷 / 02期
关键词
antithrombin deficiency; hypercoagulable; venous thromboembolism; PREVALENCE;
D O I
10.15419/bmrat.v11i2.862
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: A deficiency in antithrombin (AT) can be hereditary or acquired. It is characterized by an AT activity level that is less than 80% of normal or the lower limit of the reference range on a regular basis. In some cases, AT deficiency has been linked to an increased risk of thromboembolism. Case presentation: We present the case of a 56-year-old Malay man with long-segment thrombosis of the portal vein and superior mesenteric vein with small bowel ischemia. He was diagnosed with AT deficiency following an extensive hematological and thrombophilia workup supported by a strong familial history of venous thromboembolism (VTE) affecting his brothers and sister. Conclusion: Inherited AT deficiency must be considered when spontaneous VTE occurs in young patients with unusual localizations, such as mesenteric veins and portal veins.
引用
收藏
页码:6179 / 6182
页数:4
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