Síndrome de Anton-Babinsky / Anton-Babinski Syndrome

Introducción: El síndrome de Anton-Babinsky es un trastorno neuropsiquiátrico poco frecuente, que se manifiesta por anosognosia y ceguera cortical, debido a lesiones en las áreas visuales asociativas de la corteza occipital sin presentar afectación en la vía visual. En adultos mayores sus manifestaciones clínicas suelen ser atípicas y la valoración geriátrica integral permite orientar el diagnóstico, que se puede asociar con síndromes geriátricos. Objetivo: Describir las manifestaciones clínicas, síndromes geriátricos, paraclínicos y tratamiento de un paciente con Síndrome de Anton-Babinsky. Caso clínico: Paciente de 85 años, quien durante un postoperatorio inmediato de cirugía ocular (pterigión) presentó alteración fluctuante del estado de conciencia, alucinaciones visuales, disminución de la agudeza visual bilateral y anosognosia. La analítica sanguínea no reportó alteraciones y la tomografía computarizada de cráneo documentó isquemia occipital bilateral, se le diagnosticó síndrome de Anton-Babinsky. Conclusiones: El síndrome de Anton-Babinsky puede tener presentación atípica a través de síndromes geriátricos. La valoración geriátrica integral permite realizar un diagnóstico y manejo multicomponente oportuno con el objetivo de influir en el pronóstico tanto a corto como a largo plazo(AU)

Introduction: Anton-Babinski syndrome is a rare neuropsychiatric disorder, with a manifestation of anosognosia and cortical blindness, due to lesions in the associative visual areas of the occipital cortex without presenting visual pathway impairment. In elderly adults, its clinical manifestations are usually atypical and a comprehensive geriatric assessment allows to guide the diagnosis, which can be associated with geriatric syndromes. Objective: To describe the clinical manifestations, geriatric syndromes, paraclinical findings and treatment of a patient with Anton-Babinski syndrome. Clinical case: This is the case of an 85-year-old patient who, during the immediate postoperative period after ocular surgery (pterygium), presented a fluctuating alteration of consciousness, visual hallucinations, decreased bilateral visual acuity and anosognosia. Blood analysis reported no alterations and cranial computed tomography documented bilateral occipital ischemia; the patient was diagnosed with Anton-Babinski syndrome. Conclusions: Anton-Babinski syndrome may have an atypical presentation through geriatric syndromes. Comprehensive geriatric assessment allows for timely multicomponent diagnosis and management with the aim of influencing both short- and long-term prognosis(AU)

A rare case of cortical blindness following vaccination against SARS-CoV-2

A 61-year-old male presented with sudden loss of vision in both the eyes about 8 days after the first shot of coronavirus disease 2019 (COVID-19) vaccine (Covishield). On examination, the visual acuity was no perception of light in both the eyes. Contrast-enhanced magnetic resonance imaging (MRI) with diffusion-weighted imaging showed acute cerebral infarcts involving bilateral parieto-occipital region. Considering the temporal correlation with the vaccine shot and absence of any other precipitating factor, we hypothesized that this was probably an immunologic response to the vaccine.

Transient cortical blindness in fat embolism syndrome---a diagnostic enigma / 中华创伤杂志(英文版)

Fat embolism syndrome (FES) is a serious life-threatening manifestation of the fat embolism phenomenon characterized by Bergman's triad of dyspnea, petechiae and mental confusion. While fat embolization into systemic circulation is common, FES occurs in a meagre 0.05%-3% of patients having isolated long bone fractures. Though visual symptoms are commonly attributed to fat embolism retinopathy and is a later occurrence, it may not always be the case. Cortical blindness has been seldom reported in association with FES, and less so as a presenting complaint. Furthermore, no previous literature has described the same in context of an isolated tibia fracture. We report a 20-year-old gentleman with an isolated right tibia shaft fracture who developed sudden onset diminution of vision in both eyes less than 24 h following trauma with no other complaints. Lack of any remarkable ophthalmoscopic findings or other symptoms left us with a diagnostic conundrum. He later went on to develop altered mentation, hypoxia and generalized tonic-clonic seizures with subsequent MRI revealing multiple cerebral fat emboli also involving both occipital lobes. Supportive measures were instituted and his general condition as well as vision gradually improved following which he underwent plate fixation of the fracture under spinal anaesthesia. The perioperative period was uneventful and he was discharged following staple removal. At one month of follow-up, the patient had no residual visual field defects or neurological deficits. Though FES is rare among isolated tibia fractures, this clinical catastrophe may strike in any unsuspected setting thereby warranting a high index of suspicion to ensure early diagnosis and improved patient outcomes.

Successful management of a patient with sudden loss of vision and eclampsia complicated by posterior reversible encephalopathy syndrome

Reversible visual disturbances in patients with eclampsia may be due to either retinal detachment or retinal arteriolar vasospasm or thrombosis of the central retinal arteries or PRES (posterior reversible encephalopathy syndrome). Although retinal arteriolar vasospasm is the most common mechanism of visual disturbance, cortical blindness may occur in 1% to 15% of patients with eclampsia. Reporting herewith a case of reversible cortical blindness in the setting of severe preeclampsia complicated with eclampsia.

A pilot study regarding basic knowledge of 揷ortical visual impairment in children� among ophthalmologists

Purpose: A pilot study was done to evaluate knowledge regarding 揷ortical visual impairment (CVI) in children� among ophthalmologists. Methods: This study was conducted during the annual conference of a zonal ophthalmological society. All ophthalmologists who attended the conference were requested to participate in this study. Those who agreed were given a validated questionnaire to assess knowledge regarding CVI. Cronbach's alpha of the questionnaire was 0.6. Participants were asked to respond to multiple choice questions by choosing the single best option. The responses obtained were then evaluated. Results: The total number of registered delegates in the conference was 448. A total of 103 ophthalmologists showed interest to participate in the study with a response rate of 22.9%. Only 89/103 interested delegates were included in the study as remaining were unaware of CVI. No participant gave correct answers to all questions. Although more than 80% of them knew the most common association (87%) and site of pathology (84%), only 52% were sure about clinical features and even lesser respondents (39%) knew that magnetic resonance imaging is the correct investigation of choice. The majority responded correctly that these children need eye examination (89%) and can be managed by rehabilitation through multidisciplinary approach (82%), but only 58% could recognize differential diagnoses and had a correct idea regarding the prognosis of CVI. There was no correlation between the number of patients diagnosed per month by the respondent with knowledge of the disease. Conclusion: In this pilot study, ophthalmologists were found to have limited knowledge regarding clinical features, investigation, differential diagnosis, and visual prognosis of CVI in children. There is a need to improve awareness regarding CVI among ophthalmologists.

's experience in the treatment of cortical blindness with acupuncture: report of medical cases / 中国针灸

's experience is introduced in the treatment of cortical blindness with the comprehensive acupuncture therapy for benefiting and resolving stasis. The comprehensive therapy includes acupuncture at Sishencong (EX-HN 1), Xinming No.1 (Extra), Shang Jianming, Chengqi (ST 1), Xinming No.2 (Extra), optic area and visual area (scalp acupuncture); acupoint injection applied alternatively at Qiuhou (EX-HN 7) and Taiyang (EX-HN 5); the auricular point paste stimulation at Brain Point, Shenmen (TF), Gan (CO), Shen (CO), Yan (LO), Eye No.1 and Eye No.2; as well as the tapping therapy with skin needle at Zhengguang No.1 and Zhengguang No.2. Additionally, 3 typical cases of cortical blindness are introduced. The coordination of the different acupuncture techniques is analyzed so as to explain its actions as benefiting , resolving stasis, promoting blood circulation and nourishment of the eyes.

Porfiria aguda intermitente y su relación con el síndrome de encefalopatía posterior reversible: reporte de caso / Acute Intermittent Porphyria and it´s relationship with Posterior Reversible Encephalopathy Syndrome: Case Report

Las porfirias son un grupo heterogéneo de trastornos del metabolismo en el cual hay una deficiencia enzimática específica necesaria en la biosíntesis del grupo hemo. Dentro de estas se destaca la porfiria aguda intermitente como la forma más común, que se caracteriza por episodios de exacerbación o crisis neuroviscerales. Las manifestaciones clínicas son amplias, sin embargo, la presentación con síntomas del sistema nervioso central a diferencia de los síntomas disautonómicos o neuropáticos son poco frecuentes. Reportamos un caso que resalta la relación infrecuente entre la porfiria aguda intermitente y el síndrome de encefalopatía posterior reversible. Paciente femenina de 18 años con dolor abdominal persistente severo, hipertensión arterial, convulsiones, ceguera cortical y neuropatía axonal motora. Se le realizó una resonancia magnética nuclear (RMN) contrastada que evidenció lesiones hiperintensas corticales y cortico-subcorticales sugestivas de edema vasogénico, compatibles con síndrome de encefalopatía posterior reversible. Se hizo el diagnóstico de porfiria aguda intermitente por elevados niveles de resonancia magnética nuclear (PBG) y ácido 5-amino-levulínico (ALA) en orina y se inició tratamiento con hematina, terapia parenteral hiperglucida y el retiro de agentes porfirinogénicos. Los síntomas centrales así como los hallazgos imagenológicos se resolvieron de forma adecuada con el tratamiento. Este caso resalta la relación inusual entre la porfiria aguda intermitente y el síndrome de encefalopatía posterior reversible, en una paciente con crisis de dolor abdominal persistente, disautonomía, convulsiones, ceguera cortical y neuropatía axonal motora, síntomas que asociados nos deben sugerir estos diagnósticos.

The porphyrias are a heterogeneous group of metabolism disorders in which there is an enzymatic deficiency necessary for the pathway of heme biosynthesis. Within this group, Acute Intermittent Porphyria (AIP) is the most common disorder, characterized by episodes of neuro-visceral crisis. The clinical manifestation spectrum is wide, however symptoms originating from Central Nervous System (CNS) dysfunction are rare. We report a case that shows the infrequent relationship between AIP and Posterior Reversible Encephalopathy Syndrome (PRES) An 18-year-old female patient presented with severe persistent abdominal pain, hypertension, seizures, cortical blindness and motor axonal neuropathy. A brain contrasted MRI evidenced a cortical and cortico-subcortical high intensity lesion suggestive of vasogenic edema in frontal, parietal and occipital lobes, compatible with PRES. A diagnosis of AIP was also made due to high levels of PBG and ALA in the urine. Treatment consisted of hematin, intravenous sugar solution and the withdrawal of porphyrinogenic agents. The CNS-related symptoms and the brain lesions shown via imaging resolved appropriately with treatment. This case shows the unusual relationship between AIP and PRES, in a patient that presented with persistent abdominal pain, dysautonomia, seizures, cortical blindness and motor axonal neuropathy, symptoms that, as a whole, can suggest this diagnosis.

A Case of Posterior Reversible Encephalopathy Syndrome with Bilateral Visual Impairment

PURPOSE: To report a case of recovery of bilateral cortical blindness in a patient with posterior reversible encephalopathy syndrome. CASE SUMMARY: A 46-year-old female visited the ophthalmology department due to abrupt visual acuity decrease. Ten days earlier, she had received conservative management due to anemia caused by menorrhagia and uterine prolapse. She underwent a gynecological operation to remove a uterine myoma two days previously, and was given a blood transfusion postoperatively because of excessive bleeding. After the transfusion, she complained of acute blurred vision. Her best corrected visual acuity (BCVA) was hand motion 10 cm in both eyes. There were no abnormal specific findings except retinal dot hemorrhage at the temporal side in the left eye on fundus examination. Her pupillary light reflex was normal and optical coherence tomography examination was unremarkable in both eyes. However, flash visual evoked potential findings showed reduced P100 amplitude in both eyes and she was diagnosed with posterior reversible encephalopathy syndrome based on brain magnetic resonance imaging. After close observation without any treatment, the symptoms gradually improved. Finally, her BCVA recovered to 1.0 and P1 and P100 amplitudes were restored to normal range in both eyes at 16 weeks from the first diagnosis. CONCLUSIONS: A patient complained of bilateral visual loss without other neurological symptoms after chronic blood loss and blood transfusion. She recovered visual acuity completely with prompt diagnosis of posterior reversible encephalopathy syndrome and close observation only.

Transient Cortical Blindness Following Vertebral Angiography: A Case Report / 신경중재치료의학

Transient cortical blindness (TCB) is a rare but well-known complication of cerebral angiography. Its pathophysiology remains uncertain. We would like to report a case of TCB in a patient during a follow up vertebral angiogram for post-coil embolization of left posterior inferior cerebellar artery aneurysm. Patient's vision was resumed spontaneously within 24 hours after angiography, with no residual neurological deficit in subsequent clinical follow up. Multi-modality imaging evaluation including vertebral angiography, brain CT and MRI performed on same day are presented.

Arnold-Chiari Malformation Type III With Meningoencephalocele: A Case Report

Arnold-Chiari malformation type III (CM III) is an extremely rare anomaly with poor prognosis. An encephalocele with brain anomalies as seen in CM II, and herniation of posterior fossa contents like the cerebellum are found in CM III. The female infant was a twin, born at 33 weeks, weighing 1.7 kg with a huge hydrocele on the craniocervical junction. After operations were performed, she was referred to the department of rehabilitation medicine for poor motor development, swallowing dysfunction, and poor eye fixation at 22 months. The child was managed with neurodevelopmental treatment, oromotor facilitation, and light perception training. After 14 months, improvement of gross motor function was observed, including more stable head control, rolling, and improvement of visual perception. CM III has been known as a condition with poor prognosis. However, with the improvement in operative techniques and intensive rehabilitations, the prognosis is more promising than ever before. Therefore, more attention must be paid to the rehabilitation issues concerning patients with CM III.

Amaurosis cortical aguda secundaria a preeclampsia / Acute cortical blindness secondary to preeclampsia

La amaurosis cortical aguda es una complicación dramática y poco común de la preeclampsia. Se presenta un caso de paciente de 29 años con diagnóstico de preeclampsia grave quien describió deterioro de la agudeza visual repentino en el puerperio inmediato. El fondo de ojo fue normal. La paciente identificaba la luz intensa. Las pupilas estaban reactivas y no se observo la presencia de nistagmo. Se le realizó una resonancia magnética cuyos resultados fueron normales, por lo que se realizó el diagnóstico de amaurosis cortical aguda.

Acute cortical blindness is an uncommon and dramatic complication of preeclampsia. We present a case of a 29 years-old patient with diagnosis of severe preeclampsia who described a sudden loss of visual acuity during immediate puerperium. Fundi were normal. Pupils were reactive and there was no nystagmus A magnetic resonance were performed with normal results, because diagnosis of acute cortical blindness was done.

Anton’s Syndrome and Cortical Blindness.

Introduction: Anton’s syndrome is a condition where the patient is unaware of being blind and denies the problem even when it is pointed out to him. On the contrary, in cortical blindness patient is aware of his blindness and does not deny it. In both, bilateral lesions of the occipital lobes are seen. Case presentation: We present two cases of cortical blindness, Case 1 being consistent with diagnosis of Anton’s syndrome where patient denied of her blindness. Both cases revealed bilateral occipital lobe infarcts. Conclusions: Cerebrovascular disease is the most common cause of cortical blindness. These occur as a result of successive infarctions as seen in Case 1 or from a single embolic or thrombotic occlusion as seen in Case 2. First case is Anton’s syndrome with patient denying blindness, whereas second case is cortical blindness. It is due to involvement of other cortical centers in Anton’s syndrome that patient denies blindness.

Síndrome de Anton, el ciego que cree ver / Anton syndrome

Las manifestaciones clínicas del ACV son muy variables, no sólo la clásica hemiplejia facio-braquio-crural, déficit sensitivo contralateral y afasia, sino que también puede presentarse, en menos frecuencia, por déficit neurológicos de variada índole, tal es el caso del síndrome de Anton, en que debido a un afección del territorio cortical visual primario bilateral (área 17 de Brodmann) y al área de asociación vecina, caracterizado por ceguera cortical y anosognosia. Comunicamos el caso de un hombre que presenta este síndrome, que debido a dos ACVs, uno antiguo y otro reciente, cuyo diagnóstico fue confirmado por TAC de cerebro.

Clinical manifestations of stroke are highly variable, not only the classic hemiplegia facio-brachio-crural, contralateral sensory loss and aphasia, but can also occur, less frequently, neurological deficits of various kinds, as in the case of the syndrome in Anton, a condition that due to the territory bilateral primary visual cortex (Brodmann area 17) and the neighboring association area, characterized by cortical blindness and anosognosia. We report the case of a man who has this syndrome, due to two LCAs, one old and one recent, whose diagnosis was confirmed by brain CT.

A Case of Complete Recovery of Visual Loss Associated With Electroconvulsive Therapy

PURPOSE: To report a case of complete recovery within 1 day of cortical blindness associated with electroconvulsive therapy (ECT). CASE SUMMARY: A 15-year-old girl, who had no ophthalmologic disease, complained of bilateral visual loss immediately after ECT. At the first ophthalmologic examination, best corrected visual acuity was 0.03 in both eyes. Findings of anterior segment and fundus, movement of external ocular muscles, and pupillary light reflex were normal. Visual field examination showed generalized reduction of sensitivity and increased fixation loss in both eyes. Optical coherence tomography revealed no abnormalities. Electroretinography was normal, and a slightly prolonged latency of P100 was noted in the right and left flash visual evoked potentials. Without any specific treatment, the patient's vision improved gradually after 18 hours of ECT and was recovered completely, with vision of 1.0 in both eyes the next day. There were no abnormalities in visual evoked potentials or the visual field. CONCLUSIONS: Transient visual loss can occur after ECT, because of cortical blindness by transient cerebral ischemia, and can be recovered completely without specific treatment.

Transient Cortical Blindness following Cerebral Angiography : Case Report / 신경중재치료의학

Transient cortical blindness is a rare but well-recognized complication of cerebral angiography. A 62-year-old woman with unruptured cerebral aneurysm and a 16-year-old boy with cerebellar hemangioblastoma experienced blindness after diagnostic cerebral angiography and tumor embolization, and the symptom resolved after 1 hour and 36 hours later, respectively. We report two cases of this complication.

Bilateral Cortical Blindness Caused by Tentorial Herniation due to Brain Tumor

Two patients, one with glioblastoma multiforme (GM) in the right thalamus and the other with meningioma at the right frontal convexity, had suffered bilateral cortical blindness after transtentorial herniation. On one of those patients, bilateral cortical blindness had occurred due to acute obstructive hydrocephalus caused by GM and on the other patient, cortical blindness had developed after acute hemorrhage from meningioma. Bilateral occipital lobes of those patients showed signal change on the brain magnetic resonance image (MRI). There were no ophthalmologic abnormalities on fundoscopy and ophthalmologic examination. After recovery of consciousness, cortical blindness was detected in both patients, and during gradual recovery period, visual function was slowly recovered. The pattern of visual evoked potential (VEP) at 7 weeks and 12 weeks after herniation was normalized gradually. Cortical blindness due to herniation was reversible, even though the high signals of bilateral visual cortex still existed on MRI 16 months later in case 2.

A Case of Transient Cortical Blindness after Cardiopulmonary Resuscitation

Cortical Blindness is loss of vision due to injury of geniculocalcarine visual tract, usually caused by cerebrovascular disease. Cardiac arrest leads to global brain hypoxia or to more focal neurologic deficits. Cortical blindness is one form of these focal neurologic deficits. The severity of visual disturbance in cortical blindness is variable, so the diagnosis can be made later unless emergency physicians are familiar with it. We report a case of transient cortical blindness following hypoxic episode caused by coronary vasospasm.

Bilateral Cortical Blindness Due to Parieto-Occipital Infarction after General Anesthesia: A case report / 대한마취과학회지

Cortical blindness is characterized by visual sensation loss with retention of pupillary reaction to light, and a normal fundoscopic examination. The suggested causes are emboli, profound hypotension, anemia, and infarction of watershed areas in the parietal or occipital lobe. We experienced a case of cortical blindness with severely reduced visual acuity after penile cancer surgery under general anesthesia. In the acute stage, visual acuity was slightly improved, but over the course of several months, no further improvement in visual acuity occurred. In this case there was no severe hypotension or anemia during the operation. Two days after the operation, electroencephalography (EEG) was performed during the period of blindness and the recording obtained was abnormal, with no alpha rhythm. Biparieto-occipital lucency was found by magnetic resonance imaging (MRI). Therefore parieto-occipital infarction due to seizure, embolus, or thrombosis could be considered a possible etiology. We concluded that cortical blindness can unexpectedly develop perioperatively and postoperatively, and that close monitoring of the patient and adequate management are essential.

A case of transient cortical blindness following coronary angiography / 대한내과학회지

Transient cortical blindness is a known but rare complication occurring in 0.3~1% of patients undergoing cerebral or vertebral angiography. It is an extremely rare complication following cardiac catheterizaton and coronary arteriography. Cortical blindness is characterized by complete loss of visual perception and optokinetic nystagmus with preservation of ocular motility, pupillary responses, and normal fundoscopic examination. It has been suggested that its occurrence is due to an adverse reaction to the contrast agent, which causes an osmotic disruption of the blood-brain barrier. Patients outcome appears to be generally favorable with return of vision within 24-48 hr. We report a case of 48 year-old male patient with transient bilateral cortical blindness after coronary angiography.

Transient Cortical Blindness Following Carotid Angiography

Contrast agents are now commonly used for both diagnostic and therapeutic purposes. Complications of these agents include allergic reactions and damage to specific organs such as the kidney. But in rare cases, a temporary visual loss have been reported as our case. The 20-year-old male patient with 3cm sized cheek mass was transferred to our hospital. Initial CT findings showed a hemangioma. During follow-up survey, the mass enlarged and the pulsation was palpable. Indicating a vascular malformation, the carotid angiography checked and it was diagnosed as the A-V malformation. At 3 hours after angiography, he complained a progressive visual loss. 2 hours after onset of the visual loss, he lost his visual acuity completely. High dose steroid therapy started and he restored a complete visual acuity by 15 hours. The transient cortical blindness associated with angiography is not always due to the contrast agent. Clinical features of the cerebral embolism are identical to those of the neurotoxic effect of the contrast agent. So physicians should examine the patient carefully and other causes such as embolism, vasospasm and thrombotic event need consideration in the differential diagnosis. We experienced a case of the transient cortical blindness after the carotid angiography and review the literatures on this complication.