Cerebral venous sinus thrombosis Microchapters |
Differentiating Cerebral venous sinus thrombosis from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sharmi Biswas, M.B.B.S
Genetic or acquired conditions causing thrombosis are considered as risk factors for developing cerebral venous sinus thrombosis.
There are more than 100 different causes of cerebral venous sinus thrombosis (CVT). Virchow's principles (blood stasis, modification of vascular wall, and blood rheology) should be used to identify all the predisposing conditions for CVT. There are also some genetic and acquired causes leading to CVT. In the cohort of an International study of cerebral vein and dural sinus thrombosis(ISCVT), 34% of patients had thrombophilia while 22% of them had acquired thrombophilia.[1][2]
Genetic prothrombotic causes [1][2]
- Protein C and S deficiency
- Factor v Leiden mutation
- Resistance to activated protein C
- prothrombin mutation (A–G at position 20210)
- mutations leading to homocysteinemia
- methylenetetrahydrofolate reductase (MTHFR)
Acquired Prothrombotic States[1][2]
- homocysteinemia
- otitis
- systemic infectious diseases
- AIDS
Inflammatory Autoimmune Diseases[1][2]
- systemic lupus erythematosus
- Adamantiades-Behçet disease
- thrombotic thrombocytopenic purpura
- thrombocythemia
- severe anemia and autoimmune hemolytic anemia
- paroxysmal nocturnal hemoglobinuria
- heparin-induced thrombocytopenia
- oral contraceptives
- steroids
- illicit drugs (such as ecstasy)
- neurosurgical procedures
- jugular vein catheterization
Malignancy[2]
- CNS tumors
- '''solid''' tumors outside [[CNS]]
- dehydration, especially in children
- toxicosis
- arteriovenous malformations
- dural fistulae
- post radiation