Cerebral venous thrombosis associated to subacute De Quervain's thyroiditis in a carrier for the G20210A mutation of the prothrombin gene

被引:8
作者
Madroñero-Vuelta, AB
Sanahuja-Montesinos, J
Bergua-Llop, M
Araguás-Arasanz, C
机构
[1] Hosp Univ Arnau Vilanova, Med Interna Serv, E-25006 Lleida, Spain
[2] Hosp Univ Arnau Vilanova, Secc Neurol, E-25006 Lleida, Spain
[3] Hosp Univ Arnau Vilanova, Serv Hemostasia, E-25006 Lleida, Spain
[4] Inst Catala Salut, Ctr Atenc Primaria Prat Riba, Lleida, Spain
关键词
cerebral venous thrombosis; coagulation; hereditary disease; prothrombin gene; thrombophilia; thyrotoxicosis;
D O I
10.33588/rn.3906.2004272
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction. Recently, thyrotoxicosis has been described as a risk facior for cerebral venous thrombosis (CVT) in some reported cases. We present a case of CVT associated to a subacute De Quervain's thyriudutus in a young female who was an heterozygous carrier for the G20210A mutation of the prothrombin gene. Case report. A 42-year-old female with irrelevant past medical history developed a thrombosis of the superior sagital and right transverse sinus in the initial phase of a subacute thyroiditis. Diagnosis was made by thyroid radioactive iodine uptake, and cerebral computerized tomography scan, magnetic resonance imaging, and magnetic resonance angiography. Treatment with aspirin and corticosteroids was started until thyroid function was normalized. When CVT diagnosis was made, the patient was treated with anticoagulation. Two months later. magnetic resonance imaging showed resolution of the CVT The patient was diagnosed as an helerozygous carrier for the G20210A mutation of the prothrombin gene by genetic studies. Conclusions. Subacute thyroiditis might act as a risk factor for CVT increasing the thrombotic risk in the presence of other acquired or hereditary prothronibolic factors, such as the G20210A mutation of the prothrombin gene in our patient.
引用
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页码:533 / 535
页数:3
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