RESUMEN
Herpes Zoster (HZ) or shingles is the reactivation of the Varicella Zoster Virus (VZV), usually along a single sensory nerve, but can affect both sensory and motor cranial nerves. Major risk factors for HZ include immunosuppressed status and age older than 60 years. In the United States, the lifetime risk of HZ is approximately 30%. Worldwide, the median incidence of HZ is 4-4.5 per 1000 person-years across the Americas, Eurasia, and Australia. HZ ophthalmicus, occurring in 10-20% of patients, is an ophthalmic emergency characterized by VZV reactivation along the V1 branch of the trigeminal nerve. Approximately half of this patient subgroup will go on to develop ocular manifestations, requiring prompt diagnosis and management. While anterior segment complications are more common, neuro-ophthalmic manifestations are rarer and can also occur outside the context of overt HZ ophthalmicus. Neuro-ophthalmic manifestations include optic neuropathy, acute retinal necrosis or progressive outer retinal necrosis, cranial neuropathy (isolated or multiple), orbitopathy, and CNS manifestations. Although typically a clinical diagnosis, diagnosis may be aided by neuroimaging and laboratory (e.g., PCR and serology) studies. Early antiviral therapy is indicated as soon as a presumptive diagnosis of VZV is made and the role of corticosteroids remains debated. Generally, there is wide variation of prognosis with neuro-ophthalmic involvement. Vaccine-mediated prevention is recommended. In this review, we summarize neuro-ophthalmic manifestations of VZV.
Asunto(s)
Antivirales , Herpes Zóster Oftálmico , Herpesvirus Humano 3 , Humanos , Herpes Zóster Oftálmico/diagnóstico , Herpes Zóster Oftálmico/tratamiento farmacológico , Antivirales/uso terapéutico , Infecciones Virales del Ojo/diagnóstico , Infecciones Virales del Ojo/virología , Herpes Zóster/diagnóstico , Factores de Riesgo , Neurología , Oftalmología , Enfermedades de los Nervios Craneales/virología , Enfermedades de los Nervios Craneales/diagnósticoAsunto(s)
Enfermedades de los Nervios Craneales/terapia , Enfermedades de los Nervios Craneales/virología , Quimioterapia/métodos , Infecciones por Virus de Epstein-Barr/terapia , Linfoma de Células B Grandes Difuso/terapia , Linfoma de Células B Grandes Difuso/virología , Terapia Combinada , Humanos , Masculino , Procedimientos Neuroquirúrgicos , Adulto JovenRESUMEN
El herpes zoster ophthalmicus suele cursar con manifestaciones oculares, siendo mucho más infrecuentes las complicaciones de tipo neurológico. Una mujer de 84 años con herpes zóster en el dermatomo de la primera rama trigeminal izquierda, desarrolló una queratouveítis herpética en el ojo izquierdo a pesar del tratamiento con valaciclovir oral. A los siete días, además apareció una oftalmoplejia progresiva y total izquierda que requirió ingreso hospitalario y tratamiento intravenoso con aciclovir y corticoides. La neuroimagen fue sugestiva de un síndrome de ápex orbitario. La evolución de la oftalmoplejia fue favorable con resolución completa a los cinco meses de seguimiento, dejando una disminución de la agudeza visual por la afectación del nervio óptico. (AU)
Herpes zoster ophthalmicus usually presents with ocular manifestations, but neurological complications are much more infrequent. An 84-year-old woman with herpes zoster of the left first trigeminal branch developed herpetic keratouveitis in her left eye despite treatment with oral valaciclovir. Seven days later, a progressive and total left ophthalmoplegia appeared, requiring hospital admission and intravenous treatment with acyclovir and corticosteroids. The neuroimaging was suggestive of an orbital apex syndrome. The evolution of the ophthalmoplegia was favourable, with complete resolution at 5 months, but with decreased visual acuity due to the optic nerve involvement. (AU)
Asunto(s)
Humanos , Femenino , Anciano de 80 o más Años , Enfermedades de los Nervios Craneales/virología , Herpes Zóster Oftálmico/complicaciones , Oftalmoplejía/virología , SíndromeRESUMEN
INTRODUCTION: The COVID-19 disease emerged in Wuhan province of China in November 2019 and spread across the world in a short time, resulting in a pandemic. The first case in Turkey was detected on March 11, 2020. The aim of the current study was to reveal the effects of COVID-19 on cranial nerves by monitoring people infected with the disease based on repeated examinations and surveys. MATERIAL AND METHOD: The data of 356 patients with a positive COVID-19 polymerase chain reaction (PCR) test who received treatment between June 2020 and August 2020 in our hospital were prospectively evaluated after the study was approved by the relevant ethics committee. RESULTS: Of the 356 patients included in the study, 47 under the age of 18 years were excluded due to their unreliable examination and anamnesis findings. In addition, seven patients that died while in hospital were excluded from the study due to the lack of examination and survey records during their hospitalization. The data of the remaining 302 patients were statistically analyzed. Symptoms of cranial nerve involvement were observed in 135 patients. CONCLUSION: The COVID-19 disease caused by the SARS-CoV2 virus commonly results in cranial nerve symptoms. The fact that these findings are more common and severe in COVID-19 than previous SARS and MERS outbreaks suggests that it has a more neurotrophic and more aggressive neuroinvasion. While the negative effects of the virus on sensory functions resulting from cranial nerve involvement are evident, motor functions are rarely affected.
Asunto(s)
COVID-19/complicaciones , Enfermedades de los Nervios Craneales/epidemiología , Enfermedades de los Nervios Craneales/virología , Adulto , COVID-19/diagnóstico , COVID-19/terapia , Enfermedades de los Nervios Craneales/diagnóstico , Femenino , Hospitalización , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Evaluación de Síntomas , Turquía , Adulto JovenRESUMEN
The complete features of the neurological complications of coronavirus disease 2019 (COVID-19) still need to be elucidated, including associated cranial nerve involvement. In the present study we describe cranial nerve lesions seen in magnetic resonance imaging (MRI) of six cases of confirmed COVID-19, involving the olfactory bulb, optic nerve, abducens nerve, and facial nerve. Cranial nerve involvement was associated with COVID-19, but whether by direct viral invasion or autoimmunity needs to be clarified. The development of neurological symptoms after initial respiratory symptoms and the absence of the virus in the cerebrospinal fluid (CSF) suggest the possibility of autoimmunity.
Asunto(s)
Nervio Abducens/diagnóstico por imagen , COVID-19/diagnóstico por imagen , Enfermedades de los Nervios Craneales/diagnóstico por imagen , Nervio Facial/diagnóstico por imagen , Bulbo Olfatorio/diagnóstico por imagen , Nervio Óptico/diagnóstico por imagen , Nervio Abducens/inmunología , Nervio Abducens/patología , Nervio Abducens/virología , Adulto , Anciano , Autoinmunidad , COVID-19/inmunología , COVID-19/patología , COVID-19/virología , Enfermedades de los Nervios Craneales/inmunología , Enfermedades de los Nervios Craneales/patología , Enfermedades de los Nervios Craneales/virología , Nervio Facial/inmunología , Nervio Facial/patología , Nervio Facial/virología , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino , Neuroimagen , Bulbo Olfatorio/inmunología , Bulbo Olfatorio/patología , Bulbo Olfatorio/virología , Nervio Óptico/inmunología , Nervio Óptico/patología , Nervio Óptico/virología , SARS-CoV-2/patogenicidadAsunto(s)
COVID-19/complicaciones , Infecciones del Sistema Nervioso Central/diagnóstico , Enfermedades de los Nervios Craneales/diagnóstico , Trastornos de la Visión/diagnóstico , Adulto , Ácido Ascórbico/administración & dosificación , Azitromicina/administración & dosificación , Blefaroptosis/diagnóstico , Blefaroptosis/terapia , Blefaroptosis/virología , COVID-19/epidemiología , COVID-19/terapia , Infecciones del Sistema Nervioso Central/complicaciones , Infecciones del Sistema Nervioso Central/terapia , Enfermedades de los Nervios Craneales/terapia , Enfermedades de los Nervios Craneales/virología , Quimioterapia Combinada , Femenino , Glucocorticoides/administración & dosificación , Hospitalización , Humanos , Madagascar , Monitoreo Fisiológico , Pandemias , SARS-CoV-2/fisiología , Tiamina/administración & dosificación , Trastornos de la Visión/terapia , Trastornos de la Visión/virologíaAsunto(s)
Enfermedades de los Nervios Craneales/diagnóstico , Herpes Zóster/diagnóstico , Mononeuropatías/diagnóstico , Enfermedades del Nervio Abducens/diagnóstico , Enfermedades del Nervio Abducens/tratamiento farmacológico , Enfermedades del Nervio Abducens/fisiopatología , Enfermedades del Nervio Abducens/virología , Anciano , Enfermedades de los Nervios Craneales/tratamiento farmacológico , Enfermedades de los Nervios Craneales/fisiopatología , Enfermedades de los Nervios Craneales/virología , Diagnóstico Diferencial , Diplopía/fisiopatología , Dolor de Oído/fisiopatología , Edema/fisiopatología , Enfermedades del Nervio Facial/diagnóstico , Enfermedades del Nervio Facial/tratamiento farmacológico , Enfermedades del Nervio Facial/fisiopatología , Enfermedades del Nervio Facial/virología , Parálisis Facial/fisiopatología , Enfermedades del Nervio Glosofaríngeo/diagnóstico , Enfermedades del Nervio Glosofaríngeo/tratamiento farmacológico , Enfermedades del Nervio Glosofaríngeo/fisiopatología , Enfermedades del Nervio Glosofaríngeo/virología , Glucocorticoides/uso terapéutico , Pérdida Auditiva Sensorineural/diagnóstico , Pérdida Auditiva Sensorineural/tratamiento farmacológico , Pérdida Auditiva Sensorineural/fisiopatología , Pérdida Auditiva Sensorineural/virología , Herpes Zóster/tratamiento farmacológico , Herpes Zóster/fisiopatología , Humanos , Masculino , Mononeuropatías/tratamiento farmacológico , Mononeuropatías/virología , Osteomielitis/diagnóstico , Otitis Externa/diagnóstico , Prednisolona/uso terapéutico , Base del Cráneo , Enfermedades del Nervio Vago/diagnóstico , Enfermedades del Nervio Vago/tratamiento farmacológico , Enfermedades del Nervio Vago/fisiopatología , Enfermedades del Nervio Vago/virología , Enfermedades del Nervio Vestibulococlear/diagnóstico , Enfermedades del Nervio Vestibulococlear/tratamiento farmacológico , Enfermedades del Nervio Vestibulococlear/fisiopatología , Enfermedades del Nervio Vestibulococlear/virología , Activación ViralRESUMEN
The neurological disorders caused by Varicella Zoster Virus (VZV) in the absence of skin rash are a challenge to the clinician. The presentation varies from acute to subacute to chronic. Reactivation of VZV usually produces zoster (shingles), meningitis or meningoencephalitis, cerebellitis, isolated or multiple cranial nerve palsies (polyneuritis cranialis), myelitis, and vasculopathy. In our case, we report a 41-year-old female presented with right oculomotor, vestibulocochlear and facial neuropathies occurred 1 year before admission and making the diagnosis. There were no skin or mucosa lesions. Magnetic Resonance Imaging revealed multiple subcortical infractions in the right temporal and occipital lobes which consist with silent vasculopathy. The diagnosis was confirmed by the existence of anti-VZV IgG in cerebrospinal fluid (CSF).
Asunto(s)
Encéfalo/patología , Enfermedades de los Nervios Craneales/virología , Exantema/virología , Neuritis/virología , Adulto , Encéfalo/virología , Enfermedades de los Nervios Craneales/diagnóstico , Enfermedades de los Nervios Craneales/patología , Exantema/diagnóstico , Femenino , Herpes Zóster/virología , Humanos , Imagen por Resonancia Magnética/métodos , Mielitis/diagnóstico , Mielitis/virología , Enfermedades del Sistema Nervioso , Neuritis/diagnóstico , Neuritis/patologíaRESUMEN
Importance: Postviral olfactory loss is a common cause of olfactory impairment, affecting both quality of life as well as overall patient mortality. It is currently unclear why some patients are able to recover fully after a loss while others experience permanent deficit. There is a lack of research on the possible association between postviral olfactory loss and other cranial neuropathies. Objective: To evaluate the incidence of other cranial nerve deficits in patients with postviral olfactory loss and determine if there is an association with neurologic injury in this group. This study also sought to determine if other known risk factors were associated with postviral olfactory loss. Design, Setting, and Participants: A case-control study was conducted at a tertiary care rhinology clinic from January 2015 to January 2018 to review the incidence of cranial neuropathies in 2 groups of patients, those with postviral olfactory loss and those with chronic rhinosinusitis without olfactory loss used as a control group. Exposures: The Stanford Translational Research Integrated Database Environment (STRIDE) system was used for patient identification and data extraction. Patients with a history of olfactory loss or chronic rhinosinusitis as well as incidence of cranial neuropathies were identified by using International Statistical Classification of Diseases and Related Health Problems, Tenth Revision (ICD-10) codes. Main Outcomes and Measures: This study reviewed incidence of postviral or idiopathic cranial neuropathies in both patient groups, while also evaluating for any difference in demographic characteristics, comorbidities, or other patient-related factors. Results: There were 91 patients in the postviral olfactory loss group and 100 patients in the control group, which were age and sex matched as closely as possible. Of the 91 patients with postviral olfactory loss, mean (SD) age was 56.8 (15.3), and 58 (64%) were women; for the control group, the mean (SD) age was 57.5 (15.6) years, and 63 (63%) were women. Racial breakdown was similar across cases and controls, with white individuals making up 59% to 65%; Asian individuals, 20% to 24%; black individuals, approximately 3%; Hispanic individuals, approximately 1%; and the remaining patients being of other race/ethnicity. The incidence of other cranial neuropathies in the postviral olfactory loss group was 11% compared with 2% within the control group (odds ratio, 6.1; 95% CI, 1.3-28.4). The study also found 2 cases of multiple cranial neuropathies within a single patient within the olfactory group. Family history of neurologic disease was associated with more than 2-fold greater odds of cranial nerve deficit (odds ratio, 3.05; 95% CI, 0.59-15.68). Conclusions and Relevance: Postviral olfactory loss appears to be associated with a higher incidence of other cranial neuropathies. It is possible that there is an inherent vulnerability to nerve damage or decreased ability for nerve recovery in patients who experience this disease process.
Asunto(s)
Enfermedades de los Nervios Craneales/virología , Trastornos del Olfato/virología , Rinitis/virología , Sinusitis/virología , Estudios de Casos y Controles , Enfermedades de los Nervios Craneales/epidemiología , Femenino , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Factores de Riesgo , Tailandia/epidemiologíaRESUMEN
Good's syndrome is a primary immunodeficiency phenocopy characterized for thymoma and immunodeficiency. The most frequent clinical presentation is recurrent or opportunistic infections, hematological alterations, and chronic diarrhea. We treated a 66-year-old man who consulted for 5 days of headache and diplopia with right sixth cranial nerve palsy at examination. Patient reported chronic diarrhea and prolonged febrile syndrome accompanied by weight loss of 23 kg in the last year. Exhaustive evaluation revealed Herpes simplex virus (HSV) type 2 meningitis, eosinophilic colitis, and type A thymoma. Severe antibody deficiency (hypogammaglobulinemia) associated with thymoma confirmed the diagnosis of Good's syndrome.
Asunto(s)
Agammaglobulinemia/patología , Colitis/patología , Enfermedades de los Nervios Craneales/patología , Herpes Simple/patología , Herpesvirus Humano 2/patogenicidad , Meningitis Viral/patología , Neoplasias Glandulares y Epiteliales/patología , Neoplasias del Timo/patología , Agammaglobulinemia/diagnóstico , Agammaglobulinemia/inmunología , Agammaglobulinemia/virología , Anciano , Colitis/diagnóstico , Colitis/inmunología , Colitis/virología , Enfermedades de los Nervios Craneales/diagnóstico , Enfermedades de los Nervios Craneales/inmunología , Enfermedades de los Nervios Craneales/virología , Diplopía/diagnóstico , Diplopía/inmunología , Diplopía/patología , Diplopía/virología , Eosinofilia/diagnóstico , Eosinofilia/inmunología , Eosinofilia/patología , Eosinofilia/virología , Cefalea/diagnóstico , Cefalea/inmunología , Cefalea/patología , Cefalea/virología , Herpes Simple/diagnóstico , Herpes Simple/inmunología , Herpes Simple/virología , Herpesvirus Humano 2/crecimiento & desarrollo , Herpesvirus Humano 2/inmunología , Humanos , Recuento de Linfocitos , Masculino , Meningitis Viral/diagnóstico , Meningitis Viral/inmunología , Meningitis Viral/virología , Neoplasias Glandulares y Epiteliales/diagnóstico , Neoplasias Glandulares y Epiteliales/inmunología , Neoplasias Glandulares y Epiteliales/virología , Neoplasias del Timo/diagnóstico , Neoplasias del Timo/inmunología , Neoplasias del Timo/virologíaRESUMEN
A 53-year-old immunocompromised woman developed acute left eye blindness and paraparesis suspected to be due to neuromyelitis optica (NMO). During treatment for NMO, right eye blindness and progressive multiple cranial neuropathies developed. Cerebrospinal fluid polymerase chain reaction (PCR) revealed Varicella zoster virus (VZV). This case emphasizes the importance of considering VZV in individuals, particularly the immunocompromised, presenting with a constellation of neurological signs and symptoms, even in the absence of rash.
Asunto(s)
Ceguera/diagnóstico , Enfermedades de los Nervios Craneales/diagnóstico , Encefalitis por Varicela Zóster/diagnóstico , Lupus Eritematoso Sistémico/diagnóstico , Neuromielitis Óptica/diagnóstico , Síndrome de Necrosis Retiniana Aguda/diagnóstico , Antivirales/uso terapéutico , Ceguera/tratamiento farmacológico , Ceguera/inmunología , Ceguera/virología , Enfermedades de los Nervios Craneales/tratamiento farmacológico , Enfermedades de los Nervios Craneales/inmunología , Enfermedades de los Nervios Craneales/virología , Encefalitis por Varicela Zóster/tratamiento farmacológico , Encefalitis por Varicela Zóster/inmunología , Encefalitis por Varicela Zóster/virología , Femenino , Herpesvirus Humano 3 , Humanos , Huésped Inmunocomprometido , Lupus Eritematoso Sistémico/tratamiento farmacológico , Lupus Eritematoso Sistémico/inmunología , Lupus Eritematoso Sistémico/virología , Persona de Mediana Edad , Neuromielitis Óptica/tratamiento farmacológico , Neuromielitis Óptica/inmunología , Neuromielitis Óptica/virología , Síndrome de Necrosis Retiniana Aguda/tratamiento farmacológico , Síndrome de Necrosis Retiniana Aguda/inmunología , Síndrome de Necrosis Retiniana Aguda/virología , Activación ViralRESUMEN
Cranial polyneuropathy is commonly caused by Lyme disease. We discuss the case of a man who presented with cranial nerve deficits causing dysphagia, dysphonia and facial weakness. This diagnostic dilemma stemmed from a workup that ruled out Lyme and vascular causes leading to an expanded search for infectious explanations, which revealed varicella zoster in the cerebrospinal fluid. On review, this phenomenon is rarely reported, but has been observed with a number of herpes family viruses. In emergency department settings, clinical suspicion should be raised for VZV infection even in the absence of rash in patients that present with multiple cranial nerve palsies.
Asunto(s)
Enfermedades de los Nervios Craneales/virología , Herpes Zóster/diagnóstico , Polineuropatías/virología , Aciclovir/uso terapéutico , Antivirales/uso terapéutico , Trastornos de Deglución/virología , Disfonía/virología , Servicio de Urgencia en Hospital , Músculos Faciales/virología , Herpes Zóster/líquido cefalorraquídeo , Herpes Zóster/tratamiento farmacológico , Herpesvirus Humano 3/aislamiento & purificación , Humanos , Masculino , Persona de Mediana Edad , Debilidad Muscular/virologíaAsunto(s)
Enfermedades de los Nervios Craneales/diagnóstico , Neuritis/diagnóstico , Otitis/virología , Infección por el Virus de la Varicela-Zóster/diagnóstico , Vértigo/virología , Adolescente , Enfermedades de los Nervios Craneales/virología , Femenino , Humanos , Neuritis/virología , Nistagmo Patológico/virologíaRESUMEN
BACKGROUND: Limited data are available regarding the characteristics and prognosis of patients with stroke due to varicella zoster virus (VZV) vasculopathy. METHODS: We studied 4 patients (2 men and 2 women; age, 38-63 years) from a single center who developed acute ischemic stroke due to VZV vasculopathy. The virological diagnosis was confirmed by detecting VZV DNA and/or the IgG antibody to VZV in the cerebrospinal fluid. RESULTS: Three patients were taking immunosuppressive agents, including prednisolone and/or methotrexate, at baseline. Each patient had a characteristic skin rash prior to stroke, with the interval from rash to stroke onset ranging from 13 to 122 days. Two patients experienced antecedent cranial nerve palsies; one had the third, seventh, ninth, and 10th nerve palsies and the other had the fourth nerve palsy before stroke. Cerebral infarctions were located in the anterior circulation lesion (nâ¯=â¯1), in the posterior circulation lesion (nâ¯=â¯2), and in both lesions (nâ¯=â¯1). Intracranial arterial stenosis was only identified in one patient on magnetic resonance angiography. A high plasma d-dimer level was detected in 1 patient, whereas high ß-thromboglobulin and platelet factor 4 levels were detected in 2 patients. As a result of combined therapies with acyclovir, steroid, and antithrombotic agents, neurological symptoms markedly improved in 3 patients, whereas 1 patient was left with moderate hemiplegia. CONCLUSIONS: Cranial nerve palsies may be prodromal symptoms of VZV-associated stroke. Increased levels of thrombotic markers may support the use of antithrombotic agents, although the benefit of combined treatment should be determined through larger studies.
Asunto(s)
Isquemia Encefálica/virología , Herpesvirus Humano 3/patogenicidad , Accidente Cerebrovascular/virología , Infección por el Virus de la Varicela-Zóster/virología , Aciclovir/uso terapéutico , Adulto , Antivirales/uso terapéutico , Isquemia Encefálica/diagnóstico por imagen , Isquemia Encefálica/tratamiento farmacológico , Enfermedades de los Nervios Craneales/virología , Imagen de Difusión por Resonancia Magnética , Femenino , Fibrinolíticos/uso terapéutico , Herpesvirus Humano 3/efectos de los fármacos , Humanos , Angiografía por Resonancia Magnética , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Esteroides/uso terapéutico , Accidente Cerebrovascular/diagnóstico por imagen , Accidente Cerebrovascular/tratamiento farmacológico , Resultado del Tratamiento , Infección por el Virus de la Varicela-Zóster/complicaciones , Infección por el Virus de la Varicela-Zóster/diagnóstico , Infección por el Virus de la Varicela-Zóster/tratamiento farmacológicoRESUMEN
RATIONALE: Ramsay-Hunt's syndrome (RHS) is a disorder characterized by facial paralysis, herpetic eruptions on the auricle, and otic pain due to the reactivation of latent varicella zoster virus in the geniculate ganglion. A few cases of multiple cranial nerve invasion including the vestibulocochlear nerve, glossopharyngeal nerve and vagus nerve have been reported. However, there has been no report about RHS with delayed onset multiple cranial nerve involvement causing severe aspiration, and a clinical course that improved after more than one year of dysphagia rehabilitation and percutaneous endoscopic gastrostomy (PEG). Here, we report on a 67-year old male with delayed onset swallowing difficulty after 16 days of RHS development. PATIENT CONCERN: Severe aspiration during swallowing. DIAGNOSIS: Severe dysphagia caused by RHS with multiple cranial nerve involvement. INTERVENTION: Application of percutaneous endoscopic gastrostomy (PEG) and rehabilitation therapy of dysphagia. OUTCOMES: After 13 months from symptom onset, his PAS improved from 7 to 2 in follow-up video-fluoroscopic swallowing study (VFSS). Then, he was re-admitted, and the PEG tube was removed and oral feeding was started. LESSONS: This case gives us the lesson that optimal doses of acyclovir and corticosteroids are important to prevent progression of multiple cranial involvement in RHS, and swallowing difficulty in RHS patients with multiple cranial nerve involvement can be improved through long-term rehabilitation even if there is no improvement for more than one year.
Asunto(s)
Aciclovir/administración & dosificación , Antivirales/administración & dosificación , Enfermedades de los Nervios Craneales/terapia , Trastornos de Deglución/terapia , Herpes Zóster Ótico/tratamiento farmacológico , Corticoesteroides/administración & dosificación , Anciano , Terapia Combinada , Enfermedades de los Nervios Craneales/virología , Trastornos de Deglución/virología , Terapia por Ejercicio/métodos , Gastrostomía/métodos , Herpes Zóster Ótico/complicaciones , Humanos , Masculino , Aspiración Respiratoria/terapia , Aspiración Respiratoria/virología , Resultado del TratamientoRESUMEN
Vernet syndrome is a unilateral palsy of glossopharyngeal, vagus, and accessory nerves. Varicella zoster virus (VZV) infection has rarely been described as a possible cause. A 76-year-old man presented with 1-week-long symptoms of dysphonia, dysphagia, and weakness of the right shoulder elevation, accompanied by a mild right temporal parietal headache with radiation to the ipsilateral ear. Physical examination showed signs compatible with a right XI, X, and XI cranial nerves involvement and also several vesicular lesions in the right ear's concha. He had a personal history of poliomyelitis and chickenpox. Laringoscopy demonstrated right vocal cord palsy. Brain MRI showed thickening and enhancement of right lower cranial nerves and an enhancing nodular lesion in the ipsilateral jugular foramen, in T1 weighted images with gadolinium. Cerebrospinal fluid (CSF) analysis disclosed a mild lymphocytic pleocytosis and absence of VZV-DNA by PCR analysis. Serum VZV IgM and IgG antibodies were positive. The patient had a noticeable clinical improvement after initiation of acyclovir and prednisolone therapy. The presentation of a VZV infection with isolated IX, X, and XI cranial nerves palsy is extremely rare. In our case, the diagnosis of Vernet syndrome as a result of VZV infection was made essentially from clinical findings and supported by analytical and imaging data.
Asunto(s)
Encéfalo/virología , Enfermedades de los Nervios Craneales/virología , Herpesvirus Humano 3/inmunología , Infección por el Virus de la Varicela-Zóster/virología , Parálisis de los Pliegues Vocales/virología , Nervio Accesorio/diagnóstico por imagen , Nervio Accesorio/inmunología , Nervio Accesorio/fisiopatología , Nervio Accesorio/virología , Anciano , Encéfalo/diagnóstico por imagen , Encéfalo/inmunología , Encéfalo/fisiopatología , Enfermedades de los Nervios Craneales/diagnóstico por imagen , Enfermedades de los Nervios Craneales/inmunología , Enfermedades de los Nervios Craneales/fisiopatología , Nervio Glosofaríngeo/diagnóstico por imagen , Nervio Glosofaríngeo/inmunología , Nervio Glosofaríngeo/fisiopatología , Nervio Glosofaríngeo/virología , Herpesvirus Humano 3/aislamiento & purificación , Humanos , Imagen por Resonancia Magnética , Masculino , Nervio Vago/diagnóstico por imagen , Nervio Vago/inmunología , Nervio Vago/fisiopatología , Nervio Vago/virología , Infección por el Virus de la Varicela-Zóster/diagnóstico por imagen , Infección por el Virus de la Varicela-Zóster/inmunología , Infección por el Virus de la Varicela-Zóster/fisiopatología , Parálisis de los Pliegues Vocales/diagnóstico por imagen , Parálisis de los Pliegues Vocales/inmunología , Parálisis de los Pliegues Vocales/fisiopatologíaAsunto(s)
Enfermedades de los Nervios Craneales/diagnóstico , Infecciones Virales del Ojo/diagnóstico , Herpes Zóster Oftálmico/diagnóstico , Trastornos de la Motilidad Ocular/diagnóstico , Enfermedades Orbitales/diagnóstico , Enfermedades del Nervio Abducens/diagnóstico , Enfermedades del Nervio Abducens/tratamiento farmacológico , Enfermedades del Nervio Abducens/virología , Aciclovir/uso terapéutico , Anciano , Antivirales/uso terapéutico , Enfermedades de los Nervios Craneales/tratamiento farmacológico , Enfermedades de los Nervios Craneales/virología , Epitelio Corneal/patología , Infecciones Virales del Ojo/tratamiento farmacológico , Infecciones Virales del Ojo/virología , Femenino , Glucocorticoides/uso terapéutico , Herpes Zóster Oftálmico/tratamiento farmacológico , Herpes Zóster Oftálmico/virología , Humanos , Masculino , Trastornos de la Motilidad Ocular/tratamiento farmacológico , Trastornos de la Motilidad Ocular/virología , Enfermedades del Nervio Oculomotor/diagnóstico , Enfermedades del Nervio Oculomotor/tratamiento farmacológico , Enfermedades del Nervio Oculomotor/virología , Enfermedades del Nervio Óptico/diagnóstico , Enfermedades del Nervio Óptico/tratamiento farmacológico , Enfermedades del Nervio Óptico/virología , Enfermedades Orbitales/tratamiento farmacológico , Enfermedades Orbitales/virología , Prednisolona/uso terapéutico , Enfermedades del Nervio Trigémino/diagnóstico , Enfermedades del Nervio Trigémino/tratamiento farmacológico , Enfermedades del Nervio Trigémino/virología , Enfermedades del Nervio Troclear/diagnóstico , Enfermedades del Nervio Troclear/tratamiento farmacológico , Enfermedades del Nervio Troclear/virologíaRESUMEN
INTRODUCTION: Varicella Zoster Virus (VZV) is associated with many disorders of the central and peripheral nervous systems including neuralgia, meningitis, meningoencephalitis, cerebellitis, vasculopathy, myelopathy, Ramsay-Hunt syndrome, and polyneuritis cranialis. Cranial nerves V, VI, VII, VIII, IX, X, XI, and/or XII may be affected. The neurological disorders caused by VZV usually present with rash, but may rarely present without rash. CASE REPORT: We herein present a case of polyneuritis cranialis without rash caused by VZV affecting cranial nerves VII, VIII, IX, and X. After excluding other causes of the condition, we diagnosed VZV infection based on VZV DNA in the CSF and an elevated anti-VZV IgG level in serum. The patient responded well to antiviral therapy. CONCLUSION: VZV infection should be kept in mind during the differential diagnosis of polyneuritis cranialis; it is important to note that VZV re-activation may occur without rash.
Asunto(s)
Enfermedades de los Nervios Craneales/virología , Enfermedades del Nervio Facial/virología , Herpes Zóster/complicaciones , Herpesvirus Humano 3 , Neuralgia Posherpética/virología , Polineuropatías/virología , Aciclovir/uso terapéutico , Antivirales/uso terapéutico , Enfermedades de los Nervios Craneales/tratamiento farmacológico , Enfermedades de los Nervios Craneales/fisiopatología , Enfermedades del Nervio Facial/tratamiento farmacológico , Enfermedades del Nervio Facial/fisiopatología , Herpes Zóster/virología , Herpesvirus Humano 3/fisiología , Humanos , Masculino , Persona de Mediana Edad , Neuralgia Posherpética/tratamiento farmacológico , Neuralgia Posherpética/fisiopatología , Polineuropatías/tratamiento farmacológico , Polineuropatías/fisiopatología , Resultado del TratamientoRESUMEN
A 67-year-old woman presented with a 1-week history of left otalgia and a 1-day history of odynophagia, pain extending into the face and neck, and a productive cough. Flexible nasendoscopy showed features of supraglottitis, with swollen arytenoids and pooling of saliva in the piriform fossae. Laboratory investigations revealed a mildly raised C reactive protein. A CT scan of the neck supported the diagnosis of supraglottitis and pharyngitis, with thickening of the mucosa of the left piriform fossae and left oropharynx. Standard supraglottitis treatment was instigated, but on day 4 of the admission, a vesicular rash and features of cranial nerve involvement (V, VII, VIII, X) developed. A revised diagnosis of Ramsay Hunt syndrome with cranial polyneuropathy was made and later confirmed by varicella zoster virus PCR. After 4 weeks, facial nerve function normalised, but features of other cranial nerve palsies were persistent.