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Letter to the Editor
Visual impairment due to venous sinus thrombosis in neuro-Behçet's disease
Pérdida visual debido a trombosis de senos venosos en neuro-Behçet
F. Pérez-Bartolomé
Corresponding author
, C. Sanz-Pozo, S. Darío Rosati, E. Santos-Bueso, J. Porta-Etessam
Unidad de Neurooftalmología, Servicio de Oftalmología, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Beh&#231;et disease &#40;BD&#41; is a multisystemic inflammatory disease of unknown aetiology characterised by aphthous ulcers in the mouth and genitals&#44; ocular inflammation&#44; skin lesions including erythema nodosum&#44; and acneiform eruptions&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">1</span></a> Patients may also show neurological&#44; cardiovascular&#44; and gastrointestinal involvement&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">2</span></a> Although BD has historically been considered more prevalent in men&#44;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">3</span></a> recent studies point to a more balanced sex ratio&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">4</span></a> However&#44; most patients with neurological involvement are men&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">5</span></a> BD affects young adults&#59; age at onset is a predictive factor of clinical severity&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">6</span></a> Diagnosis is based on the presence of systemic and ocular clinical manifestations&#44; since the disease has no pathognomonic signs&#46; Ocular involvement in patients with BD usually includes bouts of inflammation occurring in the context of an underlying chronic retinal vascular inflammation&#46; Bouts may affect the anterior pole&#44; in the form of acute uveitis&#44; or the posterior pole&#44; with severe vitritis&#44; retinal haemorrhages and exudates&#44; cystoid macular oedema&#44; or optic neuritis&#46;<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">7</span></a> BD may involve the nervous system in the form of recurrent meningoencephalitis typically affecting the brainstem&#44; idiopathic intracranial hypertension &#40;ICH&#41; with or without sinus thrombosis&#44; cranial mononeuropathies&#44; cerebellar ataxia&#44; myelitis&#44; seizures&#44; and even cognitive impairment&#46;<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">8</span></a> There are 2 clearly defined forms of BD&#58; parenchymal and non-parenchymal&#46; The most frequent manifestation of the latter is venous sinus thrombosis&#46;<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">9</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">We present the exceptional case of a patient diagnosed with neuro-Beh&#231;et disease &#40;NBD&#41; and rare attacks of ocular inflammation&#46; He displayed bilateral optic atrophy secondary to chronic papilloedema in the context of ICH due to dural venous sinus thrombosis&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Our patient was a 37-year-old white man who was referred to our hospital&#39;s neuro-ophthalmology unit due to progressive and persistent vision loss in both eyes over the previous several months&#46; He had been diagnosed with BD at the age of 18 based on the presence of recurrent mouth ulcers since adolescence&#44; 2 bouts of bilateral anterior uveitis&#44; and facial acneiform eruptions&#46; At the age of 24&#44; he was diagnosed with NBD due to thrombosis of the superior longitudinal&#44; transverse&#44; and sigmoid sinuses &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41; after consulting for symptoms of headache&#44; intermittent vision loss&#44; and papilloedema&#46; He was treated with oral prednisone&#44; azathioprine&#44; colchicine&#44; ciclosporin&#44; and anticoagulants&#46; In the years previous to our evaluation&#44; our patient reported fluctuations in vision quality that were attributed to papilloedema secondary to ICH caused by dural venous sinus thrombosis&#46; Two lumboperitoneal shunts to manage ICH achieved satisfactory results and decreased papilloedema and vision loss fluctuations&#46; Mild papilloedema persisted one year later&#59; doctors suggested a permanent lumboperitoneal shunt placement but the patient refused surgery&#46; He had no other ophthalmological manifestations or relevant family history&#46; At the time of his visit&#44; he was taking oral acetazolamide&#44; azathioprine&#44; antiplatelet agents&#44; and anticoagulant agents&#46; The ophthalmological examination revealed a visual acuity of 0&#46;1 in both eyes&#46; Biomicroscopy showed pigmented keratic precipitates in both eyes and no active signs of ocular inflammation&#46; Intraocular pressure and intrinsic and extrinsic ocular motility were all within normal limits&#46; Eye fundus examination revealed bilateral papillary pallor and no signs of inflammation&#46; The Humphrey visual field test &#40;SITA-Standard 24-2 programme&#41; revealed diffuse absolute scotoma in both eyes&#46; Optical coherence tomography showed decreased thickness of the nerve fibre layer of both optic nerves &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Further analyses including a biochemical study&#44; a total protein test&#44; and measurements of folic acid and vitamins B<span class="elsevierStyleInf">1</span>&#44; B<span class="elsevierStyleInf">6</span>&#44; and B<span class="elsevierStyleInf">12</span> yielded normal results&#46; An additional lumbar puncture disclosed an intracranial pressure of 15<span class="elsevierStyleHsp" style=""></span>mm<span class="elsevierStyleHsp" style=""></span>Hg&#46; CSF analysis revealed no abnormalities&#46; Visual evoked potentials revealed no response on either side&#46; An MRI scan showed no additional findings&#46; Our patient was diagnosed with bilateral optic atrophy secondary to chronic papilloedema despite successful management of intracranial pressure&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Optic disc atrophy is an ophthalmological sequela that results in permanent interruption of axoplasmic transport in the optic nerve head&#46; In the context of BD&#44; it is usually unilateral or asymmetrical and occurs after repeated bouts of posterior uveitis &#40;vitritis&#44; vasculitis&#44; neuroretinitis&#44; optic neuritis&#41;&#46; Early loss of visual acuity and neuroretinal rim pallor are essential clinical signs for distinguishing optic disc atrophy from glaucomatous optic neuropathy&#46; As in our case&#44; NBD may contribute to damaging the optic nerve in the form of either optic neuritis or papilloedema secondary to ICH&#46;<a class="elsevierStyleCrossRefs" href="#bib0115"><span class="elsevierStyleSup">9&#44;10</span></a> In these cases&#44; involvement is usually bilateral and symmetrical&#46; The most frequent cause of ICH in NBD is dural venous sinus thrombosis&#46;<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">10</span></a> Our patient had experienced only 2 episodes of uveitis previously&#44; but ICH had been present for several years&#46; Despite good management of intracranial pressure&#44; ICH had caused papilloedema&#59; although medical and surgical treatment had achieved partial resolution of papilloedema&#44; it persisted over time&#44; leading to atrophy of the optic nerve head&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Prevalence of NBD varies greatly among studies &#40;5&#37; to 49&#37; of the cases&#41;&#46; Parenchymal involvement includes a wide range of clinical findings compatible with sensory-motor ictal symptoms&#46;<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">11</span></a> Corticosteroids&#44; immunosuppressants&#44; colchicine&#44; and biological products seem to provide good treatment options&#44; although scientific evidence is insufficient to support using them&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">12</span></a> Non-parenchymal involvement is frequently associated with signs and symptoms of ICH and mainly caused by dural venous sinus thrombosis&#46; These patients have a better prognosis than do those with parenchymal involvement&#44; which suggests that these 2 forms possess different aetiopathogenic mechanisms&#46;<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">8</span></a> Recent studies have shown that anticoagulant treatment is decisive for improving prognosis&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">13</span></a> Refractory patients and those with precisely located thrombi may benefit from mechanical thrombectomy with or without thrombolytic treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">14</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conclusion</span><p id="par0030" class="elsevierStylePara elsevierViewall">Papilloedema secondary to ICH is a rare finding in patients with NBD&#46; Prognosis is usually favourable&#44; although the condition may cause optic atrophy and even vision loss regardless of the level of previous ocular inflammation&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Funding</span><p id="par0035" class="elsevierStylePara elsevierViewall">This study has received no public or private funding&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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