Protein S deficiency with homozygous factor V Leiden mutation in central retinal vein occlusion

2007 ◽  
Vol 42 (4) ◽  
pp. 632-633 ◽  
Author(s):  
G.T. Sucak ◽  
Z. Aki ◽  
M. Or
2014 ◽  
Vol 98 (2) ◽  
pp. 190-191
Author(s):  
Rupak Roy ◽  
Kumar Saurabh ◽  
Amit B Jain ◽  
Debmalya Das ◽  
Anindya K Majumder ◽  
...  

2009 ◽  
Vol 2009 ◽  
pp. 1-2 ◽  
Author(s):  
Sarwat Salim ◽  
Wai-Ching Lam ◽  
Wahid Hanna

Purpose. To describe a patient with two episodes of deep venous thrombosis and factor V Leiden mutation who presented with central retinal vein occlusion (CRVO) despite prophylactic use of warfarin sodium (Coumadin).Methods. A case report of a 44-year-old woman with a history of recurrent deep venous thrombosis and Factor V Leiden mutation was placed on lifelong prophylactic therapy with warfarin. The patient presented with CRVO in the left eye despite therapeutic levels of warfarin.Results. Extensive systemic evaluation disclosed high titers for antinuclear antibody (ANA).Conclusion. Systemic anticoagulation with warfarin may not preclude further thrombotic episodes. In younger patients presenting with retinal vein occlusion and pre-existing multiple thrombophilic risk factors, a multidisciplinary approach is recommended to explore other therapeutic options to avoid further thromboembolic complications.


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 5054-5054
Author(s):  
Fotios I Girtovitis ◽  
Elisabet Tsakiroglou ◽  
Michael D. Diamantidis ◽  
Zoi Saouli ◽  
Zisis Kontoninas ◽  
...  

Abstract Abstract 5054 Introduction An increased risk of central retinal vein occlusion in patients with hypertension, hypercholesterolemia and diabetes mellitus has been recently shown. However, controversial literature results have failed to establish an association between central retinal vein occlusion and thrombophilic abnormalities. Aim To investigate thrombophilic factors in patients with central retinal vein thrombosis. Material and Methods 20 patients with a median age of 48±13 yrs [7 males (median age 53,2±8,4 yrs) and 13 females (median age 48,1±17,7 yrs)], who presented in the Hemostasis Unit of the First Propedeutic Department of Internal Medicine of AHEPA hospital during the last two years, were studied. All the patients suffered from central retinal vein thrombosis, which was diagnosed by fluorescein angiography. Detailed evaluation of the coagulation mechanism included examination of fibrinogen, d-dimers, thrombin time, reptilase time, protein C, protein S, antithrombin III, activated protein C resistance, factor V-Leiden and prothrombin G20210A mutation, homocystein, II, V, VII, VIII, IX, X, XI and XII coagulation factors, anti-cardiolipin antibodies, lupus anticoagulants and anti-β2 glycoprotein I. Moreover, factors of increased cardiovascular risk (obesity, hypertension, diabetes, smoking, hyperlipidemia) were studied. Results 3 male and 4 female patients suffered from antiphospholipid syndrome (APS) (5 had primary APS, 1 female had secondary APS due to systemic lupus erythematosus, while another female was diagnosed with both APS and thrombophilia Leiden). 5 patients (4 female καı 1 male) were heterozygotes for factor V-Leiden mutation. From these 5 patients, 2 were obese and had hypertension, 1 female had been receiving contraceptives, 1 other female had additionally increased levels of factor VIII (240%), whereas the fourth female suffered from additional protein S deficiency (41%). Interestingly, 4 female patients (4/20, 20%) were found to be double heterozygotes (factor V-Leiden and prothrombin mutation). In 3 females (1 of whom had a history of pulmonary embolism), the whole laboratory investigation for thrombophilic factors was negative. Increased homocysteine levels, reduced levels of natural coagulation inhibitors, along with local ophthalmic factors (i.e. glaucoma) justifying thrombosis, were traced in none of the patients. Conclusions 1) APS and thrombophilia Leiden are the most important causal factors for ophthalmic vein thrombosis. However, thrombophilia Leiden alone, does not seem responsible for causing thrombosis, since other thrombophilic factors co-existed in 8/9 patients 2) Hyperhomocysteinemia –in contrast with the results of other studies- does not appear to be a risk factor 3) The high percentage of double heterozygotes (20%) is noteworthy in the aforementioned patients. Disclosures No relevant conflicts of interest to declare.


2009 ◽  
Vol 13 (2) ◽  
pp. 155-157 ◽  
Author(s):  
Marianna Politou ◽  
Argyri Gialeraki ◽  
Efrossyni Merkouri ◽  
Anthi Travlou ◽  
Stefanos Baltatzis

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