Síndrome uveomeningoencefálico Vogt Koyanagi-Harada con desprendimiento de la capa bacilar de la retina / Vogt Koyanagi-Barada uveomeningoencephalic syndrome with detachment of the bacillary layer of the retina

Introducción: El síndrome de Vogt-Koyanagi-Harada pertenece a los síndromes uveomeníngeos y es una de las principales enfermedades que amenazan la visión. Se caracteriza por una uveítis bilateral que se asocia frecuentemente con manifestaciones neurológicas, auditivas y tegumentarias. Recientemente un fenotipo particular de engrosamiento macular se ha descrito como desprendimiento bacilar asociado a esta enfermedad. Objetivo: Describir el desprendimiento bacilar de la retina mediante la tomografía de coherencia óptica de dominio espectral en un caso de Vogt Koyanagi Harada en fase uveítica. Presentación de caso: Paciente femenina de 46 años de edad atendida en el Instituto Cubano de Oftalmología "Ramón Pando Ferrer" con disminución de agudeza visual en ambos ojos y panuveitis bilateral. Fue diagnosticada con síndrome de Vogt-Koyanagi-Harada en su fase uveítica aguda con presencia de manifestaciones neurológicas y desprendimiento de la capa bacilar de la retina identificado mediante la tomografía de coherencia óptica de dominio espectral. Conclusiones: El síndrome de Vogt-Koyanagi-Harada aguda y el desprendimiento bacilar de la capa de la retina pueden diferenciarse de otros signos mediante la tomografía de coherencia óptica de dominio espectral. Su desaparición pudiera tener una relación con la mejoría de la agudeza visual(AU)

Introduction: Vogt-Koyanagi-Harada syndrome belongs to the uveomeningeal syndromes and is one of the major vision-threatening diseases. It is characterized by bilateral uveitis, which is frequently associated with neurological, auditory and integumentary manifestations. Recently a particular phenotype of macular thickening has been described as bacillary detachment associated with this disease. Objective: To describe bacillary retinal detachment using spectral domain optical coherence tomography in a case of Vogt Koyanagi Harada in uveitic phase. Case presentation: 46-year-old female patient attended at the Cuban Institute of Ophthalmology "Ramón Pando Ferrer" with decreased visual acuity in both eyes and bilateral panuveitis. She was diagnosed with Vogt-Koyanagi-Harada syndrome in its acute uveitic phase with presence of neurological manifestations and detachment of the bacillary layer of the retina identified by spectral domain optical coherence tomography. Conclusions: Acute Vogt-Koyanagi-Harada syndrome and bacillary retinal layer detachment can be differentiated from other signs using spectral-domain optical coherence tomography. Their disappearance could be related to the improvement of visual acuity(AU)

Regarding Kaya P et al. "Predictive Factors for the Prognosis of Vogt-Koyanagi-Harada Disease".

INTRODUCTION: VKH is a primary stromal choroiditis. Studies with indocyanine green angiography (ICGA) have shown that inflammation begins at the choroid and may persist without clinically apparent inflammation. Thus, systemic therapy must target choroidal inflammation and be maintained until the choroiditis resolves, as proven by ICG and/or EDI-OCT imaging studies. DISCUSSION: Aggressive therapy with oral corticosteroids, with or without "pulsed" intravenous methylprednisolone, has been the mainstay of VKH therapy in the acute phase for many years. However, there is convincing evidence that corticosteroid monotherapy is insufficient to prevent progression onto the chronic recurrent form of the disease, which is associated with poor visual outcomes. CONCLUSION: Numerous studies suggest that combined therapy with systemic corticosteroids and immunosuppressants is necessary to prevent the progression toward chronic recurrent disease, avoiding complications, get a better control of inflammation and visual outcomes in VKH patients seen at the uveitic phase of the disease.

Infección ocular invasora por Scedosporium apioespermum en un paciente inmunocomprometido / Invasive ocular fungal infection by Scedosporium apiospermum in an immunocompromised patient

Resumen Presentamos el caso clínico de una infección fúngica invasora con una conjuntivitis necrosante, escleritis y panuveitis unilateral por Scedosporium apiospermum en una mujer de 78 años con artritis reumatoidea con neutropenia secundaria a fármacos. El diagnóstico etiológico fue confirmado por cultivo micológico de secreción ocular con apoyo de MALDI-TOF-TOF e histopatología. El tratamiento incluyó aseos quirúrgicos asociado a terapia tópica y sistémica con voriconazol y corticoesteroides, con una evolución favorable a los dos meses de tratamiento. Una recaída obligó a un segundo curso terapéutico por 12 meses adicionales con mejoría y erradicación del agente. La conjuntivitis fúngica por S. apiospermum es un evento infrecuente asociado a pacientes inmunocomprometidos. Su tratamiento involucra desbridamientos quirúrgicos y terapia antifúngica prolongada.

Abstract We report a case of invasive fungal infection with necrotizing conjunctivitis, scleritis and unilateral panuveitis caused by Scedosporium apiospermum in a 78-year-old woman that developed neutropenia by drugs indicated for rheumatoid arthritis. The etiological diagnosis was confirmed by mycological culture of an ocular secretion with the support of MALDI-TOF-TOF analysis and histopathological findings. The treatment involved surgical debridements together with topical solution and systemic therapy with voriconazole and steroids with a favorable evolution after 2 months of treatment. A relapse required a second therapeutic course for an additional 12 months with improvement and eradication of the agent. Fungal conjunctivitis due to S. apiospermum is a rare event associated with immunosuppressed patients. Its treatment involves surgical debridements and prolonged antifungal therapy.

Characteristics, Upon Presentation, of a Cohort of Patients with Vogt-Koyanagi-Harada Disease in Puerto Rico.

OBJECTIVE: To describe the clinical features, upon initial presentation, of a cohort of patients with Vogt-Koyanagi-Harada (VKH) disease who live in Puerto Rico. METHODS: A retrospective medical record review of patients with VKH was performed. The demographic and clinical characteristics were analyzed. RESULTS: Twenty-two patients who met the diagnostic criteria for VKH were identified and included in the analysis. The median age at presentation was 41 years; 68.2% were female, and all patients were Hispanics. Bilateral disease was present in 90.9% of patients, and 59.1% of patients were categorized as having probable VKH. A headache was reported in 54.5% of patients and was the most common complaint at the time of presentation; the second most common complaint was tinnitus, which was present in 22.7% of patients. Vitiligo, alopecia, and meningismus were each preset in 9.1% of patients while hearing loss and aseptic meningitis were each reported in 4.5% of patients. Seventy-seven percent of patients had either topical or systemic corticosteroid use prior to the initial encounter. CONCLUSION: Our study suggests that in Puerto Rico, patients with Vogt-Koyanagi-Harada disease may have a distinctive prevalence of characteristics at the presentation when compared to other ethnic groups, including other Hispanic cohorts.

Toxoplasmosis ocular: aspectos clínico-epidemiológicos en edad pediátrica / Ocular Toxoplasmosis: clinical-epidemiological aspects in pediatric age

RESUMEN Introducción: a nivel mundial la toxoplasmosis ocular es la causa más frecuente de uveítis posterior, se detecta principalmente en niños y adultos jóvenes. Objetivo: determinar las características clínico-epidemiológicas de la toxoplasmosis ocular en pacientes de edad pediátrica de la provincia Pinar del Río, en el período 2012-2018. Métodos: se realizó un estudio observacional analítico transversal en 39 pacientes con toxoplasmosis ocular, atendidos en consulta de Uveítis del Hospital General Docente "Abel Santamaría" entre enero 2012 y diciembre de 2018. Se estudiaron las variables: edad, sexo, factores de riesgo, síntomas, hallazgos clínicos, complicaciones y agudeza visual. Se resumieron los datos con porcentajes y se estableció asociación estadística. Resultados: la enfermedad resultó más frecuente en pacientes de 15 a 18 años (46,2 %). Las condiciones de riesgo resultaron la mala calidad del agua de consumo (100 %), y la inadecuada manipulación los de alimentos (89,7 %). Existe asociación con un nivel de significancia del 10 % (p=0,066) entre síntomas y tipo de uveítis según localización anatómica. También se detectó asociación entre MAVC con localización anatómica (p=0,001), tamaño de la lesión (p=0,011) y en menor grado con clasificación anatómica (p=0,083). La presencia de cicatriz en área macular y vasculitis se presentó en un 33,3 % y 12,8 % respectivamente. Conclusiones: la presencia de malas condiciones higiénicas resultó frecuente. Las lesiones retinianas en el área macular contribuyeron a las complicaciones y secuelas reportadas. La prevención y el tratamiento oportuno, son las mejores maneras de disminuir la ceguera por toxoplasmosis en edad pediátrica.

ABSTRACT Introduction: ocular toxoplasmosis is the most frequent cause of posterior uveitis of known etiology in the world, mainly in children and young adults. Objective: to determine the clinical-epidemiological characteristics of ocular toxoplasmosis in pediatric patients in Pinar del Río province in the period 2012-2018. Methods: an analytical cross-sectional, observational study was conducted on 39 patients with ocular toxoplasmosis, who were treated at the Uveitis clinic of Abel Santamaría Cuadrado General Teaching Hospital between January 2012 and December 2018. The variables studied were: age, sex, risk factors, symptoms, clinical findings, complications and visual acuity. Results: the disease was more frequent in patients between 15 and 18 years old (46,2 %). Risk conditions were poor quality of drinking water (100 %), and inadequate food handling (89,7%). There is association with a significance level of 10% (p=0,066) between symptoms and type of uveitis according to anatomical location. There was also association between CVMA with anatomical location (p=0,001), extent of the lesion (p=0,011) and to a lesser extent with anatomical classification (p=0,083). The presence of scar in macular area and vasculitis was evident in 33,3 % and 12,8% respectively. Conclusions: the presence of poor hygienic conditions was frequent. Prevention and timely treatment are the best ways to reduce blindness due to toxoplasmosis in children.

Ophthalmological treatment of early-onset sarcoidosis/Blau syndrome in a Colombian child: A case report.

PURPOSE: To report the ophthalmological approach of a patient with Blau syndrome (BS) in Colombia. OBSERVATIONS: We describe a 9-year-old Colombian boy with sporadic BS due to a de novo nucleotide-binding oligomerization domain containing 2 (NOD2) mutation, who presented with joint and dermatologic symptoms. He was referred to the uveitis service with a single functional eye, due to retinal detachment in the other eye. Despite treatment with corticosteroids, methotrexate, and adalimumab, the patient continued to exhibit progressive disease. CONCLUSION: BS-related uveitis is characterized by severe ocular morbidity. Appropriate interdisciplinary treatment is necessary for the correct identification and management of the disease, considering the inherent difficulty in its diagnosis due to its diverse clinical manifestations. The severity of BS-related uveitis in this report highlights the need for more effective therapies.

Panuveítis asociada a la enfermedad de Lyme en un paciente colombiano. Reporte de caso / Panuveitis due to Lyme disease in a Colombian patient: Case report

RESUMEN La enfermedad de Lyme es una zoonosis transmitida por la picadura de garrapatas del género Ixodes sp. Ha sido descrita con más frecuencia en zonas endémicas de países meridionales. Sus manifestaciones clínicas son muy variables y se presentan de acuerdo con el estadio clínico de la enfermedad, teniendo así el compromiso ocular un espectro clínico muy variado que incluye manifestaciones desde la superficie ocular hasta la inflamación del segmento posterior. Se presenta el caso de un paciente de 72 años con un viaje reciente a los Estados Unidos (EE. UU.), atendido en la consulta particular por un oftalmólogo supraespecialista en uveítis de la ciudad de Medellín. El paciente hacía un mes refería una disminución de la agudeza visual (AV) en su ojo izquierdo y al examen oftalmológico presentó signos clínicos de panuveítis no granulomatosa asociada a un edema macular y vasculitis retinal. Se confirmó la enfermedad de Lyme en fase tardía por la presencia de anticuerpos en sangre por Western blot. Se realizó tratamiento exitoso con antibióticos (doxiciclina), con recuperación de la AV y la mejoría completa de los signos inflamatorios intraoculares.

SUMMARY Lyme Disease is a zoonosis transmitted by arthropods that has been described with more frequency in endemic zones of meridional countries. Its clinical manifestations vary according to the clinical stage of the disease. The eye can be affected in many forms including the involvement of the ocular surface and the posterior segment, with more severe inflammation of the retina and the choroid. We present a case of a 72-year male with a recent trip to EEUU who complained of decreasing vision in his left eye had clinical signs of non-granulomatous panuveitis with macular edema and retinal vasculitis. Lyme disease was confirmed with positive antibodies in blood and Western blot test, and the patient was successfully treated using oral Doxycycline. His visual acuity improved and had a resolution of the intraocular inflammation after the specific treatment.

Sífilis ocular como manifestación de neurolues: a propósito de un caso clínico / Ocular syphilis as a manifestation of neurolues: about a clinical case / Sífilis ocular como manifestação de neurolores: sobre um caso clínico

Resume: La sífilis ocular es una forma infrecuente de neurosífilis, que se puede presentar en cualquier estadio de la enfermedad. La presentación clínica puede ser heterogénea, siendo la forma más frecuente la uveítis. El diagnóstico se confirma con serología, debiéndose realizar estudio del líquido cefalorraquídeo para descartar compromiso meníngeo. Su detección y tratamiento precoz permiten la prevención de complicaciones neurológicas como la ceguera irreversible. Presentamos el caso clínico de un paciente que se presenta con panuveítis y diagnóstico serológico de sífilis presentando excelente respuesta al tratamiento instaurado.

Abstract. Ocular syphilis is an uncommon type of neurosyphilis, which can occur at any stage of the disease. The clinical presentation can be heterogeneous, with uveitis being the most frequent form. The diagnosis is confirmed with serology and a study of the cerebrospinal fluid should be performed to rule out meningeal involvement. Its diagnosis and early treatment allow the prevention of neurological complications such as irreversible blindness. We present a clinical case of a patient who presents with panuveitis and serological diagnosis of syphilis presenting an excellent response to treatment.

Resumo: A sífilis ocular é uma apresentação atípica do neurosífilis, que pode ocorrer em qualquer estágio da doença. A apresentação clínica pode ser heterogênea, sendo a uveíte a forma mais frequente. O diagnóstico é confirmado com sorologia e um estudo do líquido cefalorraquidiano deve ser realizado para descartar o compromisso meníngeo. Seu diagnóstico e tratamento precoce permitem prevenir complicações neurológicas como cegueira irreversível. Apresentamos um caso clínico de um paciente com panuveíte e diagnóstico sorológico de sífilis e excelente resposta ao tratamento.

Descolamento seroso de coroide como manifestação tardia da síndrome de Vogt-Koyanagi-Harada / Serous choroidal detachment in chronic stage of Vogt-Koyanagi-Harada syndrome

Resumo Relatamos um caso atípico de uma paciente de 40 anos com apresentação completa da Síndrome de Vogt-Koyanagi-Harada (SVKH) que após 17 anos do diagnóstico inicial evoluiu com descolamento seroso de coroide. A paciente procurou atendimento com queixa de dor em olho esquerdo (OE). O exame oftalmológico revelou acuidade visual (AV) igual a de movimento de mãos, à biomicroscopia foi observada reação inflamatória granulomatosa na câmara anterior, a tonometria foi igual a 0 mmhg, e a fundoscopia indevassável pela pouca midríase e turvação de meios em OE. O descolamento seroso de coroide foi avaliado através de ultrassonografia ocular. A abordagem terapeutica intituida para paciente consistiu em prednisona 1mg/kg/dia via oral, dexametasona 1mg/mL e atropina 1% colírios. A evolução do quadro foi satisfatória, com melhora da AV para 20/40, ausência de reação inflamatória em câmara anterior, normalização da pressão intraocular e resolução do descolamento seroso de coroide em OE. Concluimos que a fase crônica da SVKH, apesar da manifestação classicamente descrita ser uveíte anterior, pode ter outras apresentações e o descolamento seroso da coroide é uma rara complicação.

Abstract We report an atypical case of a 40-year-old woman with complete presentation of Vogt-Koyanagi-Harada Syndrome (VKH) who presented with unilateral serous choroidal detachment 17 years after the diagnosis. The patient complained of pain in the left eye, the ophthalmologic examination revealed visual acuity (VA) equal to hand motion; biomicroscopy revealed a granulomatous inflammatory reaction in the anterior chamber, tonometry was equal to 0 mmhg, and the fundoscopy was impracticable. Serous choroidal detachment was assessed by ocular ultrasonography. The therapeutic approach proposed for the patient consisted of prednisone 1mg / kg / day orally, dexamethasone 1mg / mL and atropine 1% eye drops. The evolution of the condition was satisfactory, with VA improvement to 20/40, absence of inflammatory reaction in anterior chamber, normalization of intraocular pressure and resolution of serous choroidal detachment in OS. We conclude that the chronic phase of VKH, although classically described as anterior uveitis, may have other presentations and the serous choroid detachment is a rare complication.

Post-Streptococcal Uveitis: Case Report.

Background: Post-streptococcal uveitis is a rare ocular disease which is part of other auto-immune conditions associated with post-streptococcal syndrome. It was first mentioned in medical literature in 1991, with only a few cases published at that time. We are presenting the case of a patient with bilateral panuveitis subsequent to bacterial pharyngotonsillitis, with studies which had come back negative for other uveitis etiologies and which had responded very well to established treatment. Clinical Case: A case of post-streptococcal uveitis is presented with a review of current concepts of this rare eye disease.

Síndrome de Vogt-Koyanagi-Harada: Avaliação da fase da doença na qual os pacientes recebem o primeiro atendimento em serviço especializado / Vogt-Koyanagi-Harada syndrome: evaluation of the disease phase in which patients receive the first specialized attendance

Resumo Objetivo: Avaliar em qual fase da síndrome de Vogt-Koyanagi-Harada (SVKH) os pacientes recebem o primeiro atendimento em serviço especializado. Métodos: Foram analisados prontuários de 14 pacientes atendidos no Setor de Uveítes do Hospital Universitário Clementino Fraga Filho da UFRJ no período de janeiro de 2014 a março de 2017. Nesta análise, foram observados o sexo, a idade, a fase da doença e a acuidade visual destes pacientes com ao menos doença provável da SVKH. Resultados: Observamos que 35,4% dos pacientes apresentavam a doença ainda na fase uveítica e que 78,5% destes pacientes apresentava acuidade visual igual ou pior que 0,05. Destes pacientes, 78,5% eram do sexo feminino e 21,5% do sexo masculino e a mediana de idades foi de 34 anos. Conclusão: Os pacientes analisados obtiveram dificuldade em ter acesso precoce a um setor especializado, afetando assim, diretamente o tratamento e prognóstico visual.

Abstract Objective: To evaluate in which phase of Vogt-Koyanagi-Harada (VKH) syndrome the patients receive the first attendance in specialized service. Methods: A retrospective study was conduted to evaluate medical records of 14 patients with VKH in the Clementino Fraga Filho University Hospital of the Federal University of Rio de Janeiro from January 2014 to March 2017. In this analysis, gender, age, stage of disease and visual acuity of these patients with at least probable VKH were recorded. Results: Of these patients, 78.5% were female and 21.5% male and the median age was 34 years. We observed that 35.4% of the patients had the disease still in the uveitic phase and that 78.5% of these patients had visual acuity equal to or worse than 0.05. Conclusion: There is a delay in the admission of these patients to a specialized sector, thus affecting directly the treatment and visual prognosis.

Spectral optical coherence tomography findings in an elderly patient with syphilitic bilateral chronic panuveitis.

PURPOSE: To report the spectral domain optical coherence tomography (SD-OCT) features of a focal retinitis in an elderly male patient with bilateral syphilitic panuveitis. OBSERVATIONS: In the left eye (LE), spectral domain SD-OCT images during the active period revealed hyperreflectivity extending through the full thickness of the retina with no individualization of the layers, except for the retinal pigment epithelium. Once the lesion healed, SD-OCT imaging revealed an inner retinal atrophy and a mild disruption of the retinal pigment epithelium. CONCLUSIONS AND IMPORTANCE: In our patient, treponemal infection seemed to produce full-thickness retinal damage with partial involvement of the retinal pigment epithelium. The severe retinal damage, in this case, led to a poorer visual outcome than in other forms of syphilitic retinal involvement.

Bilateral Iris Depigmentation and Ocular Hypotony as End-Stage Manifestations of Untreated Vogt-Koyanagi-Harada Disease.

PURPOSE: To describe severe bilateral iris depigmentation and persistent ocular hypotony as end-stage manifestations of untreated Vogt-Koyanagi-Harada disease. METHODS: We present the clinical findings and diagnostic studies performed for three patients with bilateral iris depigmentation. RESULTS: Vogt-Koyanagi-Harada disease in late recurrent stage was diagnosed in three patients with bilateral severe iris depigmentation and persistent ocular hypotony. CONCLUSIONS: Early diagnosis and treatment of inflammation are crucial factors in the clinical outcome of Vogt-Koyanagi-Harada disease. When left undiagnosed and untreated from early stages, severe iris depigmentation and ocular hypotony, uncommon manifestations of this disease, can develop.

Characteristics of Sympathetic Ophthalmia in a Single International Center.

AIM: To report the main features of sympathetic ophthalmia in a referral ophthalmology center. METHODS: Retrospective clinical study. We reviewed clinical records of patients with diagnosis of sympathetic ophthalmia attending the Uveitis Department from 2007 to 2013. Patients were selected by clinical criteria. Descriptive statistics were used to assess variables. RESULTS: Twenty patients were included for analysis, 13 males and 7 females. Mean follow up was 1 year. The median age of presentation was 50 years. Fifty percent had history of ocular trauma and 50% had history of intraocular surgery, of which 40% underwent phacoemulsification. The time between injury and onset of symptoms ranged from 1 to 456 months. Most common ocular manifestations were mutton fat keratic precipitates and anterior chamber inflammation. All patients received oral prednisone as single or combined therapy. Sixty percent of the sympathizing eyes improved two or more lines of vision and 20% lost two or more lines of vision. CONCLUSION: This report from a single center adds to the body of literature of sympathetic ophthalmia occurring in a specific population. Our data found a high proportion of patients with sympathetic ophthalmia after phacoemulsification.

Yellowish dots in the retina: a finding of ocular syphilis? / Pontos amarelados na retina: um achado da sífilis ocular?

Here we report the occurrence of pale yellowish perivascular preretinal dots in 12 patients with ocular syphilis. A case series of these patients was examined between March and October 2012 at the Uveitis Sector of Universidade Federal de São Paulo. After diagnostic confirmation of syphilis, fundus photographs and optical coherence tomography (OCT) were performed to verify the localization of the dots, and patients were treated with IV crystalline penicillin for 14 days. The study comprised 11 men (91.6%), 19 eyes, median presentation age of 38.1 years, and panuveitis as the main clinical manifestation (seven patients, 58.3%), being bilateral in four. Ten patients were taking oral prednisone (83.3%). Serum panels performed by the Venereal Disease Research Laboratory (VDRL) showed positive results in eight patients (66.7%), whereas VDRL cerebrospinal fluid (CSF) tests were negative in seven of nine collected (77.8%). However, serum FTA-Abs was positive in 100% of patients, and eight patients (66.7%) had HIV infection. The best corrected visual acuity (BCVA) presented after treatment improved in 10 eyes (55.6%), did not change in seven eyes (38.9%), and worsened in one eye (5.6%). Although not yet acknowledged in the literature as a typical manifestation of ocular syphilis, these are very common findings in clinical practice. We believe that preretinal dots are due to perivasculitis secondary to treponema infection. It is important recognize them and remember that syphilis can present in several forms, including the one presented in this study.

Relatar a ocorrência de pontos amarelo-esbranquiçados perivasculares pré-retinianos em 12 pacientes com sífilis ocular. Série de casos de 12 pacientes examinados entre março e outubro de 2012 no setor de uveítes da UNIFESP. Após confirmação diagnóstica de sífilis ocular, retinografias e OCT (optical coherence tomography) foram realizados para verificar a localização dos pontos e os pacientes foram tratados com penicilina cristalina IV por 14 dias. Dados demográficos incluíram 11 homens (91,6%), 19 olhos, mediana de idade de 38,1 anos, e a manifestação clínica principal foi panuveíte (7 pacientes, 58,3%), sendo bilateral em 4. Dez fizeram uso de prednisona oral (83,3%). VDRL (Venereal Disease Research Laboratory) sanguíneo foi positivo em 8 pacientes (66.7%), VDRL no líquor foi negativo em 7 de 9 coletados (77,8%), FTA-Abs sanguíneo foi positivo em 100% e 8 pacientes (66,7%) eram HIV positivos, AV após tratamento melhorou em 10 olhos (55,6%), não se alterou em 7 (38,9%) e piorou em 1 olho (5,6%). Embora ainda não reconhecida na literatura como uma manifestação típica da sífilis ocular, este achado é muito comum na prática clínica. Acreditamos que esses pontos são devidos a perivasculite secundária à infecção pelo treponema. É importante os reconhecer e lembrar que a sífilis pode se apresentar de várias formas, incluindo essa apresentada aqui.

Características clínicas y diagnóstico etiológico de las uveítis virales / Clinical characteristics and etiologic diagnosis of viral uveitis

Objetivo: determinar las características clínicas y epidemiológicas de las uveítis virales según su etiología. Métodos: se realizó un estudio observacional y descriptivo transversal, que determinó el diagnóstico clínico y etiológico, según la reacción en cadena de polimerasa (PCR) de 10 ojos de pacientes atendidos en la consulta de uveítis, en el Instituto Cubano de Oftalmología «Ramón Pando Ferrer¼, de mayo a noviembre del 2010. Se utilizó una muestra de fluidos intraoculares tomada a los pacientes. Las variables analizadas fueron: edad, sexo, color de piel, antecedentes personales generales u oculares, clasificación anatómica y patológica de la uveítis, curso evolutivo, bilateralidad, agudeza visual y presión intraocular iniciales y finales respectivamente, hallazgos al fondo de ojo y resultados de la PCR. La información fue procesada y los resultados expuestos en tablas. Resultados: la edad promedio de los pacientes estudiados fue de 34,5 años, que presentaron en su mayoría episodios de uveítis anteriores unilaterales. La agudeza visual mejor corregida final mejoró con respecto a la inicial en el grupo de estudio, aunque la presión intraocular se mantuvo elevada sin lograr controlarla. El virus más hallado fue el Herpes simple. Conclusiones: los virus son responsables de producir inflamaciones oculares de presentación variada, lo que en ocasiones retrasa el diagnóstico, empeorando el pronóstico visual. En estos casos el método de PCR ha demostrado ser una herramienta útil para establecer el diagnóstico etiológico(AU)

Objective: to identify the clinical and epidemiological characteristics of viral uveitis according to their etiology. Methods: observational, cross-sectional and descriptive study to determine the clinical and etiological diagnosis, according to the plolymerase chain reaction results, of 10 eyes from patients seen at the uveitis consultation service at Ramon Pando Ferrer Cuban Institute of Ophthalmology from May to November 2010. The sample comprised intraocular fluids taken from the patients. The analyzed variables were age, sex and race, general or ocular personal background, anatomical and pathological classification of uveitis, progression, bilaterality, and initial and final visual acuity and intraocular pressure, respectively, funduscopy findings and PCR results. The collected information was processed and expressed in tables. Results: the average age of the studied patients was 34.5 years; most of them had had episodes of unilateral anterior uveitis. The final best corrected visual acuity improved when compared to the initial one of the study group, although the intraocular pressure remained high with no control. The most found virus was Herpes simplex. Conclusions: the viruses are responsible for causing ocular inflammation of varied presentations, which occasionally delays the diagnosis and worsens the visual prognosis. In these cases, the PCR method has proved to be useful tool to set the final etiological diagnosis(AU)

Características clínicas y diagnóstico etiológico de las uveítis virales / Clinical characteristics and etiologic diagnosis of viral uveitis

Objetivo: determinar las características clínicas y epidemiológicas de las uveítis virales según su etiología. Métodos: se realizó un estudio observacional y descriptivo transversal, que determinó el diagnóstico clínico y etiológico, según la reacción en cadena de polimerasa (PCR) de 10 ojos de pacientes atendidos en la consulta de uveítis, en el Instituto Cubano de Oftalmología ®Ramón Pando Ferrer¼, de mayo a noviembre del 2010. Se utilizó una muestra de fluidos intraoculares tomada a los pacientes. Las variables analizadas fueron: edad, sexo, color de piel, antecedentes personales generales u oculares, clasificación anatómica y patológica de la uveítis, curso evolutivo, bilateralidad, agudeza visual y presión intraocular iniciales y finales respectivamente, hallazgos al fondo de ojo y resultados de la PCR. La información fue procesada y los resultados expuestos en tablas. Resultados: la edad promedio de los pacientes estudiados fue de 34,5 años, que presentaron en su mayoría episodios de uveítis anteriores unilaterales. La agudeza visual mejor corregida final mejoró con respecto a la inicial en el grupo de estudio, aunque la presión intraocular se mantuvo elevada sin lograr controlarla. El virus más hallado fue el Herpes simple. Conclusiones: los virus son responsables de producir inflamaciones oculares de presentación variada, lo que en ocasiones retrasa el diagnóstico, empeorando el pronóstico visual. En estos casos el método de PCR ha demostrado ser una herramienta útil para establecer el diagnóstico etiológico

Objective: to identify the clinical and epidemiological characteristics of viral uveitis according to their etiology. Methods: observational, cross-sectional and descriptive study to determine the clinical and etiological diagnosis, according to the plolymerase chain reaction results, of 10 eyes from patients seen at the uveitis consultation service at Ramon Pando Ferrer Cuban Institute of Ophthalmology from May to November 2010. The sample comprised intraocular fluids taken from the patients. The analyzed variables were age, sex and race, general or ocular personal background, anatomical and pathological classification of uveitis, progression, bilaterality, and initial and final visual acuity and intraocular pressure, respectively, funduscopy findings and PCR results. The collected information was processed and expressed in tables. Results: the average age of the studied patients was 34.5 years; most of them had had episodes of unilateral anterior uveitis. The final best corrected visual acuity improved when compared to the initial one of the study group, although the intraocular pressure remained high with no control. The most found virus was Herpes simplex. Conclusions: the viruses are responsible for causing ocular inflammation of varied presentations, which occasionally delays the diagnosis and worsens the visual prognosis. In these cases, the PCR method has proved to be useful tool to set the final etiological diagnosis

Panuveíte em artrite indiferenciada HLA-B27 positiva / Panuveitis in HLA-B27 positive undifferentiated arthritis

Entre os vários tipos de inflamação ocular associados às doenças reumatológicas, a uveíte anterior é particularmente comum nas espondiloartropatias, em especial quando associada à presença do genótipo HLA-B27. Relatou-se o caso de um paciente com artrite indiferenciada HLA-B27 positivo, complicado com panuveíte e vasculite da retina, refratária ao tratamento imunossupressor tradicional, que obteve boa resposta clínica ao uso de anti-TNF-alfa.

Among the several types of ocular inflammation associated to the rheumatic diseases, anterior uveitis is particularly common in the spondyloarthropathies, especially when associated to the presence of the HLA-B27 genotype. We report the case of HLA-B27 positive patient with undifferentiated arthritis, complicated with panuveitis and retinal vasculitis, that was refractory to the traditional imunossupressive treatment, and had a good clinical response with anti-TNF-alpha therapy.