Neurorretinitis por Bartonella henselae en un adolescente / Bartonella henselae neuroretinitis in an adolescent

La neurorretinitis como manifestación de la enfermedad por arañazo de gato se presenta en el 1-2 % de los pacientes con afecciones oculares porBartonella henselae. Las manifestaciones oculares suelen suceder a las sistémicas, aunque pueden aparecer en ausencia de estas. La presencia de exudado macular en forma de estrella es característico y sugestivo de dicha infección. Se presenta el caso de un paciente de 14 años de edad, previamente sano, con disminución de la agudeza visual de 15 días de evolución, que ingresó por sospecha de neuritis óptica izquierda con edema de papila. El seguimiento oftalmológico reveló la aparición de la lesión característica en "estrella macular" que permitió arribar al diagnóstico de infección por B. henselae, confirmándose luego con serología positiva

Neurorretinitis as a manifestation of cat scratch disease occurs in 1-2 % of patients with Bartonella Henselae eye disease. Ocular manifestations tend to follow systemic ones, although they can appear in their absence. The presence of star-shaped macular exudate is characteristic and suggestive of this infection. We report a case of a 14-year-old healthy boy, with 15 days of decreased visual acuity, who was admitted for suspected left optic neuritis with papilledema. Ophthalmological examination revealed the characteristic "macular star" that led to the diagnosis of infection by Bartonella Henselae, later confirmed by positive serology.

Case report: Bilateral uveitis and papillitis secondary to treatment with pembrolizumab

Pembrolizumab is a programmed cell death protein 1 (PD-1) monoclonal antibody used in the treatment of metastatic melanomas. Severe ocular complications appear in less than 1% of the patients and require early treatment. We present the case of a patient diagnosed with a BRAF mutated metastatic melanoma. Ocular pain and a blurred vision appeared after treatment and the patient visited the ophthalmology emergency room, where he was diagnosed with acute anterior uveitis (AAU), synechiae, and bilateral papillitis. The patient was treated with topical corticosteroids, prednisone, and mydriatics, which immediately improved the patient's status. Therefore, when an ocular inflammatory disease exists, immune checkpoint inhibitor treatments must be ruled out as possible causes.

Analysis of the Efficacy and Safety of Compound Anisodine in the Treatment of Vascular Pseudo Papillitis / 现代医院

Objective To study of vascular false as the clinical effect and safety of acromastitis were treated by com -pound anisodine treatment , to provide reference for the treatment of vascular pseudo optic .Methods From June 2013 to June 2015, 132 cases of patients with vascular pseudo optic papilla in our hospital were selected as the observation objects , and were divided into observation group and control group each 66 cases according to the treatment method .The control group was treated with routine drug therapy , and the observation group in the control group on the basis of daily injections of Com -pound Anisodine Hydrobromide Injection .Two groups before and after the treatment of vision changes , and the treatment of safety and efficacy were compared .Results The curative effect:The two groups of patients after treatment were improved , but the observation group was significantly higher than the control group after treatment ;The cure rate and total effective rate of the observation group were 39.51%and 88.89%respectively, which was significantly higher than the control group of 24. 36%and 73.08%, and had better curative effect in observation group .Security aspect:The total incidence of adverse reac-tions in the observation group and the treatment group was 10.61%, significantly less than 24.24% of the control group, higher safety .Conclusion In the treatment of vascular pseudoaneurysms as papillitis drugs , the curative effect of compound anisodine is much better with better security , which can significantly improve the visual acuity of the patients .

Toxoplasmosis ocular. Descripción de tres pacientes con presentación atípica / Ocular toxoplasmosis. Description of three patients with an atypical presentation.

Objetivo: Describir una forma de presentación atípica de toxoplasmosis ocular, enfatizando la importancia de la jerarquización de los hallazgos clínicos y las limitaciones de la serología para realizar un diagnóstico temprano. Pacientes y Métodos: Estudio retrospectivo y descriptivo de tres casos clínicos de toxoplasmosis ocular activa, con presentación atípica (compromiso del nervio óptico), derivados al Servicio de Oftalmología del Hospital J. P. Garrahan en el periodo comprendido entre 2007 y 2010. Resultados: En los tres casos presentados la sospecha clínica de toxoplasmosis ocular no se correlacionó con evidencia serológica de infección reciente. En un caso, la terapéutica específica temprana, basada en la sospecha clínica, resultó en una excelente recuperación funcional. Un tratamiento tardío puede interferir en el resultado visual. Conclusiones: Basados en los hallazgos clínicos y la alta sospecha de esta patología debe iniciarse el tratamiento específico sin esperar que los resultados serológicos la confirmen. Eventualmente, la mejoría clínica confirmara el diagnóstico. El comportamiento de los títulos de anticuerpos en el curso de la enfermedad ocular no siempre es confiable, y en muchos casos retrasa el comienzo de la terapéutica con la consiguiente mala rehabilitación visual de estos pacientes (AU)

Objective: To describe an atypical presentation of ocular toxoplasmosis, emphasizing the importance of clinical findings and the limitations of serology in the early diagnosis. Patients and Methods: A retrospective, descriptive study was conducted of three cases with active ocular toxoplasmosis with an atypical presentation (optic nerve involvement), referred to the Department of Ophthalmology of Hospital J. P. Garrahan between 2007 and 2010. Results: In the three cases presented here clinical suspicion of ocular toxoplasmosis did not correlate with serological evidence of a recent infection. In one case, early treatment, based on clinical suspicion, resulted in excellent functional recovery. Late management may compromise visual outcome. Conclusions: Based on clinical findings and suspicion of the pathology, specific treatment should be started without waiting for serological confirmation. Eventually, clinical improvement will confirm the diagnosis. The behavior of antibody titres in the course of the ocular disease is not always reliable and often delays treatment initiation with subsequent difficulties in the visual rehabilitation of these patients (AU)

Caracterización de pacientes con neuritis óptica anterior en el Centro Oftalmológico de Santiago de Cuba / Characterization of patients with anterior optic neuritis in the ophthalmological center from Santiago de Cuba

Introducción: la neuritis óptica ha sido definida como el cuadro clínico resultante de la inflamación del nervio óptico en cualquier punto de su anatomía. Cuando la inflamación corresponde al disco óptico, se llama neuritis óptica anterior o papilitis. Objetivo: caracterizar los pacientes con neuritis óptica anterior. Métodos: se realizó un estudio descriptivo y transversal de los 48 pacientes con neuritis óptica anterior, atendidos en el Centro Oftalmológico del Hospital General Docente "Dr. Juan Bruno Zayas Alfonso" de Santiago de Cuba, del 1 de enero al 31 de diciembre del 2012. Resultados: se obtuvo un predominio de la enfermedad en el grupo etario de 21-30 años (66,6 %) y en el sexo femenino (70,8 %); en tanto, 58,0 % de la serie era de procedencia urbana y 66,6 % declaró no tener hábitos tóxicos. Igualmente, se observó que en 45,8 % la entidad era de causa infecciosa y que la mayoría de los pacientes presentaba afectación monocular (95,8 %). Conclusiones: en la provincia de Santiago de Cuba, la neuritis óptica anterior se manifestó con mayor frecuencia en mujeres y personas jóvenes, con primacía del origen infeccioso. Los hábitos tóxicos no parecieron estar relacionados con la aparición de la oftalmopatía.

Introduction: the optic neuritis has been defined as the clinical resultant pattern of the optic nerve swelling at any point of its anatomy. When the inflammation corresponds to the optic disk, it is called optic neuritis or papillitis. Objective: to characterize the patients with anterior optic neuritis. Methods: a descriptive and cross-sectional study of the 48 patients with anterior optic neuritis, assisted in the Ophthalmological Center of "Dr. Juan Bruno Zayas Alfonso" General Hospital in Santiago de Cuba was carried out from January 1st to December 31st, 2012. Results: a prevalence of the disease was obtained in the age group 21-30 years (66.6%) and in the female sex (70.8%); as long as, 58.0% of the series had an urban origin and 66.6% declared not to have toxic habits. Equally, it was observed that in 45.8% the disease had an infectious cause and that most of the patients presented monocular damage (95.8%). Conclusions: the anterior optic neuritis showed a higher frequency in women and young people in Santiago de Cuba province, with primacy of the infectious origin. Toxic habits seem not to be related to the emergence of the ophthalmopathy.

A Case of Ocular Syphilis Presenting as Bilateral Optic Neuritis

PURPOSE: To report a case of ocular syphilis presenting as bilateral optic neuritis. CASE SUMMARY: A 25-year-old man presented with visual difficulty in both eyes that had begun 2 weeks previously. Best corrected visual acuity was 0.7 in the right eye and 0.1 in the left eye. Anterior segment was normal. On fundoscopic examination, optic disc swelling was found in both eyes. Color vision was abnormal in the left eye. The visual field (VF) showed peripheral constriction in the right eye and generalized reduction in the left eye. Fluorescein angiography revealed early, bilateral leakage of dye from the optic disc with multiple hot spots in the chorioretinal level. Serology was positive for fluorescent treponemal antibody absorbance (FTA-ABS) IgM, IgG and rapid plasma reagin test. A test of the cerebrospinal fluid was positive for venereal diseases research laboratory and FTA-ABS IgG. A diagnosis of syphilitic optic neuritis was made and the patient was treated with antibiotics. Six months later, visual acuity was 1.0 in the right eye and 0.8 in the left eye. There was no disc swelling on both fundoscopy and optical coherence tomographs. VF also improved after treatment, with the restoration of central vision. CONCLUSIONS: Syphilis can present as optic neuritis. Clinicians should consider serologic examination for syphilis and then initiate appropriate antibiotic treatment.

Neuritis óptica por picadura de abeja / Optic neuritis after a bee sting

La neuritis óptica es la inflamación aguda del nervio óptico y su forma atípica se produce por la inflamación del nervio óptico como parte de un proceso de causa infecciosa, inmune, granulomatosa, o por contigüidad. Las picaduras por himenópteros (abejas, avispas, hormigas) han sido asociadas con diferentes cuadros clínicos, que van desde manifestaciones locales hasta cuadros sistémicos como anafilaxis, glomerulonefritis y afectación del sistema nervioso central (lesiones vasculares e isquémicas, neuritis óptica y lesiones desmielinizantes). Desde 1960 se han documentado casos de neuritis ópticas asociadas a las picaduras de himenópteros, que adoptan las formas de neuritis óptica anterior isquémica e inflamatoria. Se presenta el caso de una paciente, mujer de 62 años de edad, que luego de tres días de haber sufrido picadura por abeja en párpado inferior izquierdo, presentó disminución de la agudeza visual de ambos ojos y escotoma central, concomitante con cefalea y dolor ocular bilateral exacerbado con los movimientos oculares. Al examen oftalmológico la agudeza visual se encontraba disminuida (visión en bultos). En el fondo de ojo se evidenció de forma bilateral discos ópticos de bordes borrados. En la resonancia magnética ocular se observó engrosamiento hiperintenso del nervio óptico izquierdo. Por las características clínicas y el antecedente epidemiológico se planteó el diagnóstico de neuritis óptica bilateral. Se inició pulsos de metilprednisolona, con posterior mejoría de la clínica.

Optic neuritis is an acute inflammation of the optic nerve and, in its atypical form, is caused by inflammation of the optic nerve as part of infectious, immune, granulomatous, or contiguity processes. Hymenoptera stings (bees, wasps and ants) have been associated with different clinical presentations, ranging from local events to systemic manifestations, such as anaphylaxis, glomerulonephritis and central nervous system involvement (ischemic vascular lesions, optic neuritis and demyelinating lesions). This is a report of the case of a 62-year-old woman that after three days of being stung by a bee in the left lower eyelid, showed decreased visual acuity of both eyes and central scotoma, concomitant bilateral headache and eye pain, exacerbated by eye movements. The ophthalmological examination showed that visual acuity was decreased and the bilateral fundus examination revealed blurred optic disks edges. Hyperintense thickening of the left optic nerve was observed with an ocular MRI. Due to the clinical manifestations and epidemiological history, the diagnosis of bilateral optic neuritis was established. Treatment with pulses of 1g/daily of methylprednisolone was initiated, for three days, with clinical improvement within 24 hours after receiving the first dose. Since 1960, cases of optic neuritis associated with hymenoptera stings have been documented, which take the form of anterior optic neuritis. A case of a patient who presented clinical features of bilateral optic neuritis after been stung by a bee, with a good clinical outcome after treatment with methylprednisolone is reported.

Presumed Ocular Toxoplasmosis Presenting as Isolated Unilateral Papillitis

PURPOSE: To report an atypical case of ocular toxoplasmosis presenting as isolated unilateral papillitis. CASE SUMMARY: A 53-year-old female presented with visual difficulty in her right eye that had begun 1 week previously. Best corrected visual acuity was 0.8 in the right eye and 1.0 in the left eye. On fundoscopic examination, optic disc swelling and focal edema with hard exudates in the nasal parapapillary retina were found in her right eye. Fluorescein angiography revealed marked leakage of dye from the swollen optic disc. There was no evidence of vasculitis and chorioretinitis. Pupillary light reflex and color vision were normal. Visual field (VF) showed generalized reduction in the right eye, and was normal in the left eye. Optical coherence tomography (OCT) revealed right optic disc swelling. Serology was positive for toxoplasma IgM and IgG. The patient was treated with oral steroids and antitoxoplasma antibiotics. Two months later, visual acuity was 1.0 in the right eye. There was no disc swelling on fundoscopy or OCT and VF was normal. CONCLUSIONS: Ocular toxoplasmosis can present atypically as isolated papillitis without chorioretinitis and mimic idiopathic optic neuritis. A thorough serologic examination for toxoplasmosis along with proper treatment should be performed.

Management of optic neuritis.

Optic neuritis is an inflammatory condition of the optic nerve characterized by a sudden onset of unilateral visual loss, usually affecting young females. Demyelination associated with multiple sclerosis (MS) is the most common cause in regions where MS is prevalent; while in other places, there are a substantial proportion of cases where infective or autoimmune causes are seen. Optic Neuritis Treatment Trial (ONTT) was the first major study that provided information on the natural history, role of steroids in treatment and risk of development of MS. Subsequently, numerous clinical trials have evaluated different modalities of management of optic neuritis and MS. The Controlled High-Risk Subjects Avonex Multiple Sclerosis Prevention Study (CHAMPS); the Prevention of Relapses and Disability by Interferon β-1a Subcutaneously in Multiple Sclerosis (PRISMS) Trial; and, most recently, the Betaferon in Newly Emerging Multiple Sclerosis for Initial Treatment (BENEFIT) Study have provided large amount of information on the natural history of optic neuritis and management options available. However, due to the low prevalence of MS reported in Asian studies, high cost of therapy and indefinite time period of treatment, it may not be cost effective to start interferon therapy in most cases.

Acute Optic Neuritis in Children : Clinical Features, Visual Outcome, Recurrence Rate, and Subsequent Evolution into Multiple Sclerosis / 대한소아신경학회지

PURPOSE: Acute optic neuritis is an inflammatory optic neuropathy, and rarely occurs in children. Childhood-onset optic neuritis is different from adult-onset optic neuritis in terms of clinical and prognostic aspects. We investigated the clinical characteristics and visual prognosis related to the steroid therapy in children with acute optic neuritis. In addition, we evaluated the recurrence rate of acute optic neuritis and subsequent evolution into multiple sclerosis. METHODS: The medical records of ten children, who were previously admitted for acute optic neuritis at the Department of Pediatrics of Ajou University Medical Center from January 1995 to April 2004, were retrospectively reviewed. Nine patients were treated with intravenous methylprednisone pulse therapy, 0.5-1.0 g/day, for 3-5 days followed by an oral prednisone therapy. To 30 months after discharge, we followed up a long-term visual prognosis, recurrence rate and subsequent evolution into multiple sclerosis. RESULTS: There were 4 boys and 6 girls and the mean age of onset was 10 years. Bilateral optic neuritis was noticed in 8 children and 9 children presented with papillitis. Etiology of acute optic neuritis was idiopathic in 50% of patients. Of the remaining cases, it was related with acute disseminated encephalomyelitis(30%), sinusitis(10%), and neuromyelitis optica(10%). Orbital MRI showed optic nerve enhancement and/or enlargement and optic disc protrusion in 15 of the 18 examined eyes. Visual evoked potential (VEP) was abnormal in 12 of the 16 examined eyes; P100 response was totally attenu ated in 6 eyes, and in the others the amplitude of P100 response was normal but the latency was delayed. On follow-up VEP at 1 month after steroid pulse therapy, the amplitude of P100 response was normalized in all, but the latency was still delayed in 60% of the patients. A short-term visual acuity after treatment with steroid was normally recovered in 14 of 15 involved eyes. Acute optic neuritis recurred in one of the nine patients who were treated with high dose methylprednisone pulse therapy, but there was no subsequent development of multiple sclerosis during the follow up. CONCLUSION: The most common cause of acute optic neuritis in children is idiopathic, and presents as bilateral papillitis. On this study, a short-term visual prognosis after high dose methylprednisone pulse therapy is extremely good, but there was no significant difference in long-term visual prognosis at 6 months after treatment with steroid. Acute optic neuritis in children does not usually recur, and does not evolve into multiple sclerosis.

Polypoid Stenosing Papillitis of the Ampulla of Vater / 대한소화기내시경학회지

Stenosing papillitis is a descriptive term for an anatomic deformity of the Ampulla of Vater due to chronic inflammation and fibrosis, which is characterized by narrowing of the lower end of the bile and pancreatic duct, and by clinical symptoms resembling pancreticobiliary disease. Duodenoscopic finding of "stenosing papillitis" usually shows edema, erythema, and laceration on Ampulla of Vater, but endoscopic finding such as polypoid mass is rare. We recently experienced one case of polypoid stenosing papillitis and report with a review of relevant literatures A 54-year-old man was admitted to our hospital because of chronic right upper abdominal pain for 2 years. Duodenoscopy re-vealed a polypoid mass with erythemaous color change on Ampulla of Vater, which was endoscopically resected by using a polypectomy snare, and pathologic examination showed chronic inflammation and fibrosis.

A Case of Papillophlebitis in 21-year-old Healthy Male Adult

Papillophlebitis is a central retinal vein occlusion with papillitis and usually occurs in a young healthy adult. It is usually unilateral and symptoms include mild visual impairment, floaters of metamorphopsia. In contrast to central retinal vein occlusion in old age, there is usually no association with diabetes, hyopertension and cardiovascular disorder. Usually the retinal hemorrhage resolves spontaneousaly after several months and the papillitis decreases with good visual outcome. The authors experienced a papillophlebitis in 21-year-old male with sudden visual decrease of left eye. He had no systemic diseases. The patient recovered good vision with systemic steroid treatment. We report this case with review of previous reports.