Bilateral Occlusion of the Central Retinal Vein due to Excess of Factor VIII Level
Article Information
Bencharef H1*, Kouame H1, Oukkache B1,2
1Biological Hematology Department, Ibn Rochd University Hospital, Casablanca, Morocco
2Casablanca Faculty of Medicine and Pharmacy, Hassan II University Casablanca Morocco
*Corresponding Author: Hanaa Bencharef, Biological Hematology Department, Ibn Rochd University Hospital, Casablanca, Morocco.
Received: 27 April 2023; Accepted: 12 May 2023; Published: 16 June 2023
Citation:
Bencharef H, Kouame H, Oukkache B. Bilateral Occlusion of the Central Retinal Vein due to Excess of Factor VIII Level. Archives of Clinical and Medical Case Reports. 7 (2023): 271-275.
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Introduction: Retinal vein occlusion (RVO) is an obstruction of the retinal venous system, frequently linked to cardiovascular risk factors in elderly; it remains rarer in young subjects, and requires a rigorous etiological investigation. In this article we report the first case of bilateral central retinal vein occlusion (CRVO) in a young patient related to excess factor VIII levels.
Case Presentation: A 22-year-old woman presented with a complaint of sudden and bilateral decreased visual acuity. The patient had no particular pathological history. The best-corrected visual acuity was reduced to light perception in both eyes. A complete fundus assessment including retinal angiography showed bilateral occlusion of the central retinal vein with areas of ischemia.
A complete assessment of thrombophilia was performed revealing an isolated excess of the plasma factor VIII level at 226.4%, checked on a second sample at 232%. The diagnosis of thrombophilia secondary to an increase in factor VIII responsible for OCRV was retained, and the patient was treated with panretinal photocoagulation in both eyes with specialized treatment in the hematology department. For her clinical course, at the visual level her state is stationary in light perception, and at the renal level, she continues her hemodialysis sessions at the rate of 3 sessions per week.
Conclusion: An elevated factor VIII level is an independent risk of venous thrombosis. Moreover, it is likely to influence the pathogenesis of central venous occlusion of the retina. These patients should be carefully evaluated to diagnose thrombophilia, including factor VIII, and initiate appropriate management as soon as possible.
Keywords
Central Retinal Vein Occlusion; Factor VIII; Thrombophilia; Venous Thrombosis
Central Retinal Vein Occlusion articles; Factor VIII articles; Thrombophilia articles; Venous Thrombosis articles
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Article Details
1. Introduction
Retinal vein occlusion (RVO) is an obstruction of the retinal venous system that may involve the central retinal vein or one of its branches [1]. It is the second common cause of retinal vascular disease after diabetic retinopathy, which represents a major source of morbidity and can lead to permanent visual impairment [2]. The visual loss is due to macular edema, retinal ischemia, and ocular neovascularization [3].
RVOs are more common in the elderly [4] and are frequently linked to cardiovascular risk factors [5] including hypertension, dyslipidemia, diabetes, etc. In younger people, thrombophilia remains the main cause of retinal vascular disorders [6, 7]. Thrombophilias can be heritable – such as factor V Leiden (FVL), the prothrombin gene G20210A mutation (PGM) [8], deficiencies of the natural anticoagulants protein C (PC), protein S (PS), or antithrombin (AT), elevated factor VIII (FVIII) levels [9] – or acquired, particularly the antiphospholipid syndrome-lupus anticoagulant [10].
Elevated plasma levels of factor VIIIc are known to be a significant, independent and dose-dependent risk factor for venous thromboembolism (VTE) [11], and have been reported in patients with RVO in several investigations [12-14]. We report a case of bilateral occlusion of central retinal vein (CRVO) in a young patient associated with an excess of the plasma level of FVIII.
2. Observation
A 22-year-old woman with no specific pathological history presented to the emergency room with sudden bilateral blindness.
Her visual acuity was less than 1/20th, reduced to light perception in both eyes. The fundus examination showed papillary edema with dilated retinal veins and some flaming hemorrhages suggesting occlusion of the central retinal vein.
A retinal angiography was performed showing bilateral occlusion of the central retinal vein with areas of ischemia (Figure 1).
Figure 1: Retinal angiography showing bilateral occlusion of the central retinal vein with areas of ischemia.
Antithrombine |
123 % [70-140 ] |
Protéine C |
150 % [70-140 ] |
Protéine S |
116 % [70-140 ] |
Factor VIII level |
232 % (First sample) [70-140 %] 226, 4 % (Second sample) |
Anti-phospholipid antibodies : - 'Lupus'-Type Circulating Anticoagulant - Anti-cardiolipin - Anti-beta2 glycoprotein1 |
Absence |
Resistance to activated protein C |
0, 77 sec [0. 58-1.10] |
Homocysteinemia |
9 umol/l [3, 9-10, 7] |
Factor V Leiden mutation |
Absence |
Prothrombin gene G20210A mutation |
Absence |
Table 1: Complete assessment of thrombophilia.
A standard laboratory workup was performed including a complete blood count with a normal platelet count at 230 G/L [150 – 450 G/L] and a routine hemostasis workup with a normal Prothrombin time at 105% [70-140%], Activated partial thromboplastin time at 28 seconds [23-33 sec] and a normal fibrinogen level at 2.89 g / l [2-4 g/l]. Given the bilaterality of the CRVO and the young age of the patient, a complete assessment of the thrombophilia was carried out, which was normal overall, except for the factor VIII level which was high at 232%, checked on a second sampling at 226.4% [70-40%] (see Table 1).
Immunoassay for markers of autoimmune diseases and vasculitis was free from abnormalities with absence of anti-MBG antibodies (glomerular basement membrane) and ANCA (Antineutrophil cytoplasmic antibodies) antibodies. According to this clinical presentation and laboratory results , the diagnosis of thrombophilia secondary to an increase in factor VIII; responsible for OCRV, was retained, and the patient was treated with panretinal laser photocoagulation performed in both eyes. Her clinical course at the visual level is stationary in light perception, and at the renal level, she continues her hemodialysis sessions at a rate of 3 sessions per week. For thrombophilia, the patient was referred to a hematologist to start anticoagulant therapy and for specialized follow-up.
3. Discussion
The pathogenesis of RVO is not yet fully understood. As a vein occlusion, it can be related to the Virchow triad: hemodynamic changes (venous stasis), degenerative changes in the vascular wall and blood hypercoagulability [15]. Several risk factors have been described for the development of this disease [16-18]. Strong evidence from different studies shows an increased risk of RVO in patients with arteriosclerosis [19, 20]. Over the past years, several groups have evaluated the possible role of thrombophilia in RVO pathogenesis [21, 22].
The Leiden Thrombophilia study (LETS) was the first to report an association between elevated plasma levels of FVIII and veinous thrombosis [23]. Factor VIII is a plasma glycoprotein which plays an essential role in the intrinsic coagulation pathway as a cofactor of activated factor IX (FIXa) and thus allows the activation of factor X [24]. Once activated by thrombin, activated factor VIII (FVIIIa) detaches from von Willebrand factor and forms a complex with factor IXa, leading to a marked acceleration of factor X activation [25].Then prothrombin is converted to thrombin, which in turn converts soluble fibrinogen into insoluble fibrin. Therefore, an elevated Factor VIII level stimulates thrombin formation and increases platelet activation and fibrin formation, a process which may contribute to the development of occlusive thrombi [26, 27].
The association between high levels of factor VIII: C and venous thrombosis has been confirmed by other studies which have also shown that factor VIII is an independent risk factor for thrombosis and that this relationship is a dose-dependent phenomenon [9, 23, 28-30]. It has even been included as a thrombophilia factor [31].
Our patient had a sudden visual loss due to bilateral occlusion of the retinal vein, linked to a high level of factor VIII level, as the only abnormality found in the screening of thrombophilia. Different studies have incriminated the high level of Factor VIII as a risk factor for the development of CRVO (Table 2).
STUDIES |
CASES |
CONTROLES |
P value |
||
Number (n) |
Hight FVIII: C (%) |
Number (n) |
Hight FVIII: C (%) |
||
Faude et al 2004 [32] |
62 CRVO |
53 |
107 |
19.7 |
0.0004 |
Glueck et al 2005 [3] |
44 RVO |
10 |
40 |
0 |
0.041 |
Glueck et al 2008 [34] |
40 CRVO |
30 |
80 |
5 |
0.0002 |
Glueck et al 2012 [33] |
132 CRVO |
20 (23/116) |
105 |
7 (7/98) |
0.008 |
Dixon 2016 [35] |
76 RVO |
42 |
62 |
11 |
< 0.0001 |
Bucciarelli 2017 [36] |
313 RVO |
11, 3*(28/248) |
415 |
4, 8 (20/415) |
0.032 |
* Information not available for 65 patients.
Table 2: Studies that evaluated the prevalence of elevated Factor VIII in RVO.
Faude et al [32] reported that 53% of 62 patients with CRVO had an elevated factor VIII greater than 150% (> 150 IU) compared to 19.7% of the healthy control group. This difference in factor VIII: C activity between cases and controls was very significant (p = 0.0004); suggesting that high factor VIII activity is likely to influence the pathogenesis of central retinal vein occlusion. In another study [3] , elevated levels of hereditary factor VIII were more common in RVO patients (n = 44) than in controls (n= 40) (10% vs 0%). On a larger sample including 132 CRVO and 105 controls, Glueck et al [33] concluded that CRVO cases were more likely than controls to have high Factor VIII (OR 2.47, 95% CI: 1.31-7.9), and this has also been reported by others [34, 35].
In a recent case-control study [36] involving 313 patients with confirmed RVO and 415 healthy individuals, elevated factor VIII (FVIII) levels were independently associated with an increased risk of RVO. Lately in 2019, Chang et al [37] published a case report of a patient who had a combined occlusion of the central retinal vein and artery due to elevated factor VIII levels, and suggested that these patients should be carefully assessed to diagnose underlying factors, including factor VIII, to initiate appropriate management as soon as possible. Otherwise, in 1003 acute unilateral CRVO (41 ischemic // 62 non-ischemic), elevated levels of FVIII were found as a risk factor for the ischemic form of CRVO (OR, 6.17; 95% CI, 2, 56-14, 82; p <0.001) [38] which is the case in our patient. To our knowledge, this is the first case describing « bilateral occulsion » of the central retinal vein related to elevate Factor VIII in the literature. The dosage of Factor VIII must be systematically included in the assessment of thrombophilia, its increase is a known and proven cause of venous or arterial thrombosis. It is necessary to think of this etiology especially in front of the young age and the negativity of the other parameters of the assessment of the thrombophilia.
4. Conclusion
RVO is associated with multiple contributing factors, including thrombophilia and cardiovascular risk factors. Known as a risk factor for venous thrombosis, elevated level of Factor VIII is also involved in the development of RVO. The diagnosis of an underlying thrombophilia including Factor VIII is important not only for the management of the RVO but to prevent other potentially life-threatening thrombotic events such as pulmonary embolism.
Declaration of Interest
The submitted manuscript has been approved by all the authors who declare that they have no conflict of interest in connection with this article. The manuscript has not been published elsewhere, it has not been submitted to another review, and is not being reviewed by another publication.
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