Inflammatory Sixth Nerve Palsy Post-COVID-19 Vaccination: Magnetic Resonance Imaging Findings.

Sixth nerve palsy is the most common post-vaccination oculomotor palsy. It is generally transient with most patients making a complete recovery. We report the case of a 46-year-old healthy male patient who presented with a painless sixth nerve palsy after the second dose of the Pfizer BioNTech COVID-19 vaccine, which recovered over the course of the next month. We confirmed the lesion localisation by demonstrating enhancement of the root exit zone and the cisternal portion of the sixth nerve on sequential magnetic resonance imaging during the symptomatic period. Here, a temporal relationship between vaccine application and diplopia onset suggests an aetiologic relationship. Moreover, the lack of pre-existing medical conditions suggests a post-vaccination inflammatory process.

Visual Loss after Platelet-rich Plasma Injection into the Face.

Platelet-rich plasma has become one of the most widely used facial cosmetics fillers. We evaluated four patients treated by cosmetologists with platelet-rich plasma injections who developed irreversible blindness due to iatrogenic occlusion of the ophthalmic artery; immediately after the injection in the glabellar area in three cases and in the nasolabial fold in one case. Early after the injections the fundi of all patients demonstrated central retinal artery and choroidal occlusions. Later, two patients developed retinal pigment dispersion and one of them a pigmented optic disc. The scars on the skin showed similar characteristics in all patients, which could constitute an important marker in the presumptive diagnosis of platelet-rich plasma injection associated complications.

Ocular flutter following Zika virus infection.

Zika virus (ZIKV) is an emerging flavivirus which has been linked to a number of neurologic manifestations such as Guillain-Barré syndrome (GBS), transverse myelitis, and meningo-encephalitis. Ophthalmologic manifestations are increasingly being reported; however, ocular dyskinesias have not been described in this context to date. Herein, we report a case of a 22-year-old female who presented with ocular flutter and associated Guillain-Barré syndrome following acute ZIKV infection. We speculate that although such symptoms may have originated from a direct viral insult, a post-infectious autoimmune mechanism may not be excluded. Physicians should include ZIKV as well as other flaviviruses in their diagnostic workup for all patients with ocular flutter/opsoclonus, after excluding other non-infectious causes of central nervous system pathology. To the best of our knowledge, this is the first report on the association of ocular flutter, GBS, and ZIKV infection.

Optical coherence tomographic artefacts in diseases of the retinal pigment epithelium.

AIMS: To show optical coherence tomography (OCT) artefacts in images from patients with retinal pigment epithelium detachment and retinal laser scars when OCT protocol analyses were applied. METHODS: All OCT retinal scans using OCT-3000 (software 4.02) were reviewed over a three-month period. 13 eyes of 11 patients were selected for this study. 10 eyes had retinal pigment epithelial detachments and 3 had retinal laser scars. All patients had ophthalmic examination, fluorescein angiography (one had indocyanine green angiography) and OCT. All OCT processing and analysis protocols were applied in each case. RESULTS: 10 eyes of 8 patients with retinal pigment epithelial detachments showed flattening of the retinal pigment epithelium and apparent inversion of the dome of the detachment when scan protocol analyses were applied. 3 eyes with retinal laser scars displayed thinning of the retinal pigment epithelium without changes behind the scar. The retinal tissues around the lesions did not show any alteration. CONCLUSIONS: OCT scan analysis is an excellent method to obtain specific information about the retina. However, some lesions that cause disruption of external reflectivity (retinal pigment epithelium) can cause software-related artefacts when analysis protocols are applied. To prevent diagnostic error, re-evaluation of the clinical fundus examination should be considered in any patient in whom OCT findings do not appear consistent with the initial clinical findings.

Association between sleep apnea syndrome and nonarteritic anterior ischemic optic neuropathy.

OBJECTIVE: To determine if patients with nonarteritic ischemic optic neuropathy (NAION) have sleep apnea syndrome (SAS), an entity characterized by repetitive upper airway obstructions during sleep, inducing hypoxia and sleep disruption. METHODS: We recruited 17 patients with NAION and 17 age- and sex-matched controls from patients referred for treatment because of suspected restless legs syndrome. We performed overnight polysomnography and determined the respiratory disturbance index during night sleep, a value used to diagnose and grade SAS. We compared the proportions of patients with SAS among patients with NAION and matched controls using the chi(2) test. Additionally, we compared the proportions of patients with SAS among patients with NAION and a large SAS prevalence study using the binomial test. RESULTS: Twelve (71%) of 17 patients with NAION had SAS. According to the respiratory disturbance index, 4 patients (24%) had mild, 4 patients (24%) had moderate, and 4 patients (24%) had severe SAS. Only 3 (18%) of 17 controls had SAS (P =.005). In the 45- to 64-year age group, 4 (50%) of 8 patients with NAION had SAS; 51 (11.9%) of 430 of the random sample in the prevalence study had SAS (P =.005). In the group older than 64 years, 8 (89%) of 9 patients with NAION had SAS; 18 (24%) of 75 of the random sample in the prevalence study had SAS (P<.001). CONCLUSIONS: We found a high prevalence of SAS in patients with NAION, which supports previous case reports suggesting that such an association exists. This association may explain why approximately 75% of all patients with NAION discover visual loss on first awakening or when they first use vision critically after sleeping. Our findings indicate that SAS may play an important role in the pathogenesis of NAION.

Repeat reliability of the multifocal visual evoked potential in normal and glaucomatous eyes.

PURPOSE: To investigate the repeat reliability of the multifocal visual evoked potential (mfVEP). PATIENTS AND METHODS: Fifteen subjects with no known abnormalities of the visual system and 10 patients with glaucoma participated in the study. Monocular mfVEPs were recorded on two separate days, using a 60-sector, pattern-reversal dart board array. Within a single session, two 7-minute. recordings were obtained for each eye. The amplitude of each mfVEP response was obtained using a root mean square measure (RMS). An mfVEP ratio [10*log (RMS day 1 / RMS day 2)] provided a measure of the reproducibility of an individual response. The same calculations were performed for Run 1 compared with Run 2 within a day and Run 1 (Run 2) compared with Run 1 (Run 2) across days. RESULTS: For all 1800 mfVEP responses (60 sectors x 15 subjects x 2 eyes), the correlation between the amplitude on day 2 and the amplitude on day 1 was good (r = 0.85). The mean standard deviation (SD) of the 60 mfVEP ratios for the individual subjects was 1.63 dB for the 14-minute records (the combination of the two 7-minute recordings). On average for the 7-minute records, the mean SD across days was 1.77 dB while the mean SD within a day was 1.53 dB. The correlation within a day (r = 0.87) also was slightly larger than across days (r = 0.80). The mean SD decreased as the RMS amplitude increased. The patients' mean SD was 1.75 dB with r equal to 0.82. CONCLUSIONS: The repeat reliability of the mfVEP was good (approximately 1.6dB); in fact, it was better than that typically obtained with static automated perimetry (approximately 2.7dB). Repeat testing on separate days added surprisingly little to the variability seen with repeat testing within the same session.

Síndrome adyuvante por implante de protesis mamarias de silicón (siliconosis): ¿una condición emergente? / Adjuvant syndrome due to silicone breast prosthesis implant (siliconosis): an emergent condition?

Los implantes mamarios de silicona se han asociado con una variedad de condiciones médicas que aparecen en coincidencia con su implantación; ello constituye la emergencia de una nueva y poco conocida patología de la modernidad. Más del 87% de los enfermos sintomáticos, presentan neuropatía desmielinizante y axonal, comprobada en la biopsia de nervio y músculo, mientras que aproximadamente el 22%-25% tienen evidencia de enfermedad tiroidea autoinmune. Un pequeño porcentaje del 10%-12%, presentan enfermedad desmielinizante primaria del sistema nervioso: esclerosis múltiple diagnósticada mediante resonancia magnética y estudios de líquido cefalorraquideo. Otros presentan condiciones inmunológicas diversas como síndrome de fibromialgia, tiroiditis de Hashimoto, polimiositis, dermatomiositis, lupus eritematoso sistémico, artritis reumatoide, esclerodermia y presencia de autoanticuerpos. Para estos pacientes sintomáticos se propone como diagnóstico unitario un síndrome adyuvante por implante de prótesis mamarias de silicon. Se presentan los casos de dos pacientes ilustrativos.

Silicone breast prosthesis has been associated with a variety of medical conditions or autoimmune diseases, which has coincidental relation with the implants insertion; it's loomed as a new and unknown pathology of the modern times. More than 87% of symptomatic patients developed demyelination axonal neuropathy demonstrated by nerve and muscle biopsy; 22% to 25% have evidence of autoimmune thyroid disease. An a small group of patients (10%-12%) have primary central nervous system demyelination disease as. multiple selerosis. The diagnosis of multiple selerosis was corroborated by magnetic resonance imaging and cerebrospinal fluid analysis. Also, an other wide spectrum of immunological diseases have been observed, such as fibromyalgia. Hashimoto's, polymyositis, dermatomyositis, lupus erythematosus, rheumatoid arthritis, scleroderma, and the presence of autoantibodies. Finally, for symptomatic patients, an adjuvant syndrome of silicone breast prosthesis or implant is proposed as a unitary diagnosis. The authors presented two patients whom illustrated this entity.

Migraña oftalmopléjica: variantes y secuelas: comunicación de cuatro observaciones / Ophthalmoplegic migraine: variants and consequences: communication of four observations

La migraña oftalmopléjica es una condición de la infancia caracterízada por crisis de severa cefalea hemicraneal seguida de parálisis ipsolateral de los nervios tercero, cuarto o sexto. Modernamente se explica mediante la teoría trigémino-vascular de la migraña. Aunque suele ser autolimitada puede dejar secuelas. Los autores comunican los casos de cuatro pacientes: tres niños con parálisis del tercer nervio craneal: una de ellas, desarrolló en el tiempo una regeneración aberrante secundaria, situación excepcional descrita en la literatura internacional en menos de diez pacientes. El último, un adulto con dos episodios de parálisis del sexto nervio craneal y una del tercer nervio. Se discuten sus manifestaciones clínicas y neurorradiológicas.

Ophthalmoplegic migraine in childhood is a painful migraine or headache complicated by an isolated III, IV or VI oculo-motor nerve palsy followed by total resolution without sequelae. The pathogenesis is unclear, however, more recently an hypothesis of trigeminovascular system activation have been proposed. The authors reported four patients with ophthalmoplegic migraine: three children with third cranial nerve palsy; one of them developed secondary aberrant regeneration of the third nerve. It is an exceptional case, because in the international literature less than ten patients had been reported. One case was an adult patient with recurrent nerve palsy (two episodes of sixth cranial nerve palsy and one event of third nerve palsy). Clinical and neuroradiological manifestations are discussed.

No todo es diversión: papiledema y montana rusa / Not everything is fun: papilledema and roller coaster

Presentamos el caso de una paciente de 30 años de edad previamente saludable, quien desarrolló luego de numerosos viajes en una montaña rusa un hematoma subdural espontáneo y un higroma contralateral. La estroma velocidad y despliegue de fuerza G, la sucesión de momentos de aceleración y desaceleración, los bruscos movimientos cefálicos con tironeo lateral del cerebro y el número de veces que permitió el viaje, constituyeron un riesgo significativo de ruptura de venas puente, siendo posible que las reiteradas caídas de una boya remolcada hayan constituido el último trauma y desencadenamiento final

We present the case of a 30-year-old previously healthy patient, who developed ofter numerous trips on a roller coaster a spontaneous hematoma subdural and a contralateral hygroma. Extreme speed and G-force deployment, the succession of moments of acceleration and deceleration, sudden cephalic movements with snarling side of the brain and the number of times that he repeated the trip, they constituted a significant risk of rupture of veins bridge, being possible that repeated falls from a towed buoy have produced the latest trauma and final trigger

"La obstrucción estaba abajo": tumores de la médula espinal e hipertensión intracraneal

Aumento de la presión intracraneal, hidrocéfalo y papiledema son observados ocasionalmente en pacientes portadores de tumores medulares en la región cervical o en la unión craneocervical, y entre otros, la obstrucción mecánica de la circulación del líquido cefalorraquídeo es asumida como responsable para tales síntomas y signos. No obstante, la hipertensión intracraneal es un raro fenómeno en tumores espinales de localización tóracolumbar. Los autores describen dos pacientes en quienes un tumor en tal localización (schwannoma benigno y paraganglioma) se asoció a síntomas de hipertensión intracraneal, hidrocefalia y papiledema. Se piensa que este tipo de lesiones puede interferir activamente en la dinámica del flujo del líquido cefalorraquídeo en razón de que la ocupación de espacio impide la expansión del saco dural y espacio subaracnoideo espinal que se piensa juegan algún papel en la compensación de los cambios de volumen y la presión intracraneal

Increased intracranial pressure, hydrocephalus and papilledema are occasionally observed in patients harboring spinal tumors in the cervical region or at the craniocervical junction, and among others, the mechanical obstruction to the cerebrospinal fluid circulation is assumed to be responsible for such symptoms and signs. However, increased intracranial pressure is very rare in spinal tumors located in the thoraco-lumbar region. Two patients are described by the authors in whom a benign thoracolumbar tumor (benign schwannoma and paraganglioma) was associated with symptoms of increased intracranial pressure, hydrocephalus and papiledema. It has been suggested that this kind of lesions could actively interfere with cerebrospinal fluid dynamics by their mass effect, especially by preventing the expansion of the dural sac and spinal subarachnoid space which may play some roce in compensating for volume changes and intracranial pressure

Ambliopía refractiva / Refractive amblyopia

Se hizo un estudio retrospectivo de 1.950 historias de pacientes, tomando como base la refracción bajo cicloplejía y la mejor agudeza visual alcanzada con corrección, el patrón para establecer ambliopía fue una agudeza visual de 10/30 o peor. Resultaron 205 pacientes con ambliopía (10.51 por ciento), de ellos 102 (49,7 por ciento) por defectos refractivos. La diferencia de refracción entre los dos ojos determinó la cantidad de anisometropía. El valor refractivo mínimo que causó ambliopía para astigmatismo fue 2 dioptrías, para hipermetropía 2 dioptrías y para miopía 5 dioptrías. Para una cantidad determinada de defectos, los miopes alcanzaron mejor AV que los pacientes con astigmatismo e hipermetropía

Enoftalmos pulsátil en neurofibromatosis tipo I (NF-1): comunicación de tres casos clínicos y revisión de la literatura / Pulsating enophthalmos in neurofibromatosis type I (NF-1): communication of the three clinics cases and revition of literature

El enoftalmos pulsátil asociado a NF-1 es una condición extremadamente rara. En la literatura internacional revisada, apenas hallamos 6 comunicaciones previas de la condición. Todos los informes, con excepción de uno en que se describen dos casos, están constituídos por una sóla observación. El presente informe describe las historias clínicas y los hallazgos imagenológicos (tomografía computarizada y resonancia magnética cerebrales), de tres enfermos evaluados en la Unidad de Neuro-Oftalmología del Hospital Vargas de Caracas en un período de 20 años, lo que eleva a 9, el número de casos descritos. En todos ellos existía neuroma plexiforme palpebral superior, displasia esfenoidal, encefalocele esfeno-orbitario, hipoplasia del seno maxilar, ausencia de tumores asociados, aumento de volumen orbitario y en uno, se demostró por resonancia magnética, prolapso de la grasa orbitaria en la fosa subtemporal. Se plantea que estos dos últimos elementos explican la producción de un enoftalmos y no, su contrapartida más frecuente, el exoftalmos pulsátil

Glaucoma sine glaucoma: introducción al disco excavado en Neuro-Oftalmología / Glaucoma sine glaucoma: introduction a the excavate disk in neuro-ophthalmologics

Con el objetivo de introducir al oftalmólogo en el reconocimiento de los discos excavados no glaucomatosos, los autores inicialmente revisan los elementos clínicos y oftalmoscópicos diferenciales entre el glaucoma verdadero y el glaucoma de presión normal. Posteriormente, utilizando como recurso didáctico la presentación de las historias clínicas de cuatro pacientes femeninas con discos excavados unilateralmente, tres de las cuales albergaban aneurismas del segmento carótido-oftálmico y una de ellas, un adenoma hipofisario, que comprimían el nervio óptico intracraneal, intentan familiarizarlo con los discos excavados no glaucomatosos y sus características distintivas más resaltantes. Así, la presencia del dolor cefálico o facial de variada intensidad, constituyó un sensible marcador de enfermedad intracraneal. La severa reducción de la agudeza visual de las pacientes contrastó y fue desproporcionada al pobre desarrollo de la excavación. Los defectos del campo visual fueron inusuales para glaucoma, predominando el escotoma central y defectos alineados con el meridiano vertical. Se menciona que las estrategias utilizadas en la campimetría computarizada de Humphrey no suelen demostrar escotomas centrales, los cuales deben ser investigados por procedimientos sencillos como la campimetría por confrontación, la rejilla de Amsler o la pantalla tangente de Bjerrum. Con relación a la inspección del disco óptico, fue la regla la predominancia de la palidez por sobre la profundidad de la excavación

Meningioma de la vaina del nervio optico y venas optociliares: su demostración mediante el empleo combinado de angiografía fluoresceínica y angiografía digital con verde de indocianina / Harboring optic nerve sheath, meningiomas and collateral optociliary veins in whom conmbined fluorescein angiography and digital indocyanine green angiography

Describimos cuatro pacientes con meningioma de la vaina del nervio óptico primarios y secundarios y vasos colaterales optociliares de diversos grados de desarrollo a quienes se realizó combinadas, angiografía fluoresceínica del fondo ocular y angiografía digital con verde de indocianina. De esta forma fue posible trazar claramente el trayecto de estas colaterales desde su origen en tributarias de la vena central de la retina, su unión a venas coroideas y su desembocadura en el sistema de venas vorticosas. Se notó una relación inversa entre el grado de elevación del disco óptico y el desarrollo de las venas retinociliares. Es la primera vez que estas colaterales son demostradas "in vivo" por un método fotográfico.