RESUMEN
Graves orbitopathy (GO) is rare in pediatric patients, however is the most common extrathyroid manifestation of Graves disease (GD), being present in 30-67% of patients. GO is an autoimmune inflammatory disorder involving orbital connective and fatty tissues as well as the extraocular muscles. In children, GO is less common and less severe than in adults. The most common symptoms are upper eyelid retraction, conjunctival injection, and proptosis and periorbital edema. Severe complications include dysthyroid optic neuropathy, corneal ulceration and eyeball subluxation. The diagnosis is established by clinical, laboratory and imaging findings. There are no management guidelines for GO in children but adult recommendations include the assessment of clinical activity and its severity, to implement the best treatment. Supportive therapies are intended to relieve symptoms and prevent corneal damage in mild cases. Tobacco exposure should also be avoided. The first line of treatment is systemic administration of corticosteroids in active and severe cases. Other options as somatostatin use and retrobulbar radiation have not been used in children, therefore their use is not recommended.
Asunto(s)
Humanos , Niño , Adolescente , Oftalmopatía de Graves/diagnóstico , Oftalmopatía de Graves/etiología , Oftalmopatía de Graves/fisiopatología , Oftalmopatía de Graves/tratamiento farmacológico , Factores de Riesgo , Glucocorticoides/uso terapéuticoRESUMEN
La Orbitopatía de Graves se presenta clínicamente en aproximadamente 50 por ciento de los casos de Enfermedad de Graves. La mayoría de las veces es leve y sólo en menos del 5 por ciento pone en riesgo la visión, pese a lo cual deteriora significativamente la calidad de vida de los pacientes. Hasta el momento no se conoce totalmente la patogenia, siendo posiblemente el receptor de TSH el blanco de la autoinmunidad. En cuanto al tratamiento, las medidas preventivas como lograr el eutiroidismo y la suspensión del tabaco son útiles en los distintos grados de la enfermedad. Para los casos más severos se han investigado diferentes medicamentos pero ninguno ha demostrado ser superior a los Glucocorticoides. Actualmente los consensos concuerdan en que es imprescindible clasificar al paciente según grado de actividad y severidad para orientar la terapia con mayor eficacia. Las investigaciones en curso pretenden encontrar una droga que supere el rendimiento existente
Graves' orbitopathy occurs clinically in approximately 50 percent of Graves' Disease. Most often it is mild and only less than 5 percent can threaten vision, despite which it significantly impairs the quality of life of this patients. So far its pathogenesis is not completely understood, but possibly TSH receptor is the target of autoimmunity. In relation to treatment, preventive measures such as achieving euthyroidism and the suspension of tobacco are useful in varying degrees of the disease. For more severe cases, different drugs have been investigated but none has shown superior efficacy to that of Glucocorticoids. Currently, different consensus agrees that it is essential to classify the patient according to levels of activity and severity to guide therapy more effectively. Ongoing investigations aim to find a drug that exceeds the existing performance
Asunto(s)
Humanos , Oftalmopatía de Graves/etiología , Oftalmopatía de Graves/terapia , Enfermedades de la Tiroides/complicaciones , Enfermedades de la Tiroides/terapia , Índice de Severidad de la Enfermedad , Somatostatina/análogos & derivados , Somatostatina/uso terapéutico , Fumar/efectos adversos , Cese del Uso de Tabaco , Oftalmopatía de Graves/inmunología , Glucocorticoides/uso terapéuticoRESUMEN
A Doença de Graves é um processo imunológico em que a combinação de fatores genéticos e ambientais é fundamental. Vários genes têm sido propostos como envolvidos no desenvolvimento da doença, particularmente os genes do sistema HLA e os polimorfismos do gene CTLA-4. Com relação à Oftalmopatia de Graves, além dos fatores genéticos, o tabagismo é conhecido como um importante fator de seu desenvolvimento. Nós previamente demonstramos que a herança de polimorfismos em genes relacionados ao metabolismo e detoxificação de xenobióticos, além de genes relacionados a apoptose celular, como TP53, tem uma importante ação na suscetibilidade para essas doenças. Nosso objetivo foi determinar as relações entre o polimorfismo do gene CTLA-4 região promotora -318, CYP1A1m1, GSTP1 e 72TP53 e os riscos para Doença de Graves e Oftalmopatia de Graves. Avaliar a relação entre fatores clínicos (idade, sexo, etnia, tabagismo, tamanho do bócio), laboratoriais (TSH, T4livre, T3total, ANTITPO, antiTg, TRAb), de imagem (captação tiroidiana com tecnécio ou iodo131) e de tipo de tratamento (radioiodo, drogas antitiroidianas e cirurgia) . Estudamos um total de 193 pacientes com Doença de Graves comparados com 200 indivíduos-controle, pareados por idade e etnia. A análise genética foi realizada através de PCR-RFLP em DNA extraído de sangue periférico. Confirmando nossos dados anteriores, as variantes dos genes GSTP1 (p = 0,0007) e CYP1A1m1 (p < 0,0001 ) eram mais frequentes em pacientes com Doença de Graves do que em controles, mas isso não ocorreu com o gene CTLA-4, região promotora -318 (p = 0,12) ou nas variantes 72TP53 (p = 0,27). Estudando o mesmo polimorfismo na Oftalmopatia de Graves, observamos que o genótipo...
Graves' disease is an immunologic process in which the combination of environmental and genetic factors is fundamental. Various genes have been proposed as involved in the development of the disease, particularly HLA system genes and the polymorphisms of CTLA-4 gene. Concerning Graves' ophthalmopathy, besides the genetic factor, smoking is a well accepted factor of its development. We previously demonstrated that the inheritance of polymorphisms in genes related to the metabolism and detoxification of xenobiotics, such as CYP1A1 and GSTP1 genes, besides the genes related to cellular apoptosis, such as TP53, have an important role in the susceptibility to these diseases. Our objective was to determine the relationship among CTLA-4 gene and CYP1A1m1, GSTM1, GSTP1 and 72TP53 genes in the risk for Graves' disease. We studied a total 193 Graves' disease patients compared to 200 control individuals, matched for age and ethnicity. The genetic analysis was done with the use of PCR-RFLP in DNA extracted from peripheral blood. Reinforcing our previous data, GSTP1 (p=0.0007) and CYP1A1m1 (p<0.0001) variants were more frequent among Graves' disease patients than in controls, but this did not happen to CTLA-4 position 318 (p=0.12) or to TP53 variants...
Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Persona de Mediana Edad , Enfermedad de Graves/cirugía , Enfermedad de Graves/genética , Enfermedad de Graves/radioterapia , Hipertiroidismo , Hipertiroidismo/complicaciones , Bocio , Oftalmopatía de Graves/etiología , Polimorfismo GenéticoRESUMEN
PURPOSE: To investigate the immunohistochemical expression (IGF-1, EGFr, EGF, c-erbB-2/HER-2/neu, PDGF-A, PDGF-B, FGF and VEGF) in patients with Graves' ophthalmopathy. METHODS: Twenty-four samples (Graves' ophthalmopathy patients) underwent lateral rectus muscle and surrounding fibrous and adipose tissue biopsy. The control group was obtained by strabismus surgery. Correlation between clinical- ophthalmologic, endocrinological, ultrasonographic findings, and immunohistochemical expression was performed. RESULTS: IGF-1: There were 7 positive cases (29.2 percent). There was a direct relation with higher CAS (clinical activity score) in all of them and if only CAS equal or higher than 5 was considered, this was 54.5 percent. FGF: There was expression in 5 cases (20.8 percent) with a direct relation in all those with higher CAS (>5) (45.4 percent). VEGF: There were two positive cases (8.3 percent) for VEGF in endothelial cells, in these cases the patients also presented CAS higher than 5. There was no expressions of all growth factors in the control group. CONCLUSIONS: All patients, except one, with positive expression of FGF, IGF-1 and VEGF showed CAS greater than 5, suggesting in this way an important role of these growth factors in the pathogenesis and severity of Graves' ophthalmopathy. However, statistical analysis revealed only significant association between IGF-1 and male sex (P=0.034). Low ultrasound reflectivity and endocrine status may not correlate directly with disease activity or with immunoexpression of growth factors and c-erbB-2/HER-2/neu.
OBJETIVO: Investigar a expressão imuno-histoquímica de IGF-1, EGFr, EGF, c-erbB-2/HER-2/neu, PDGF-A, PDGF-B, FGF e VEGF na oftalmopatia de Graves. MÉTODOS: Vinte e dois pacientes (oftalmopatia de Graves) foram submetidos à biópsia do músculo reto lateral e tecido fibroso e adiposo adjacente. O grupo controle foi de pacientes de cirurgia de estrabismo. Foi feita correlação entre achados clínico-oftalmológicos, endocrinológicos, ultra-sonográficos e da expressão imuno-histoquímica dos fatores de crescimento. RESULTADOS: IGF-1: Houve 7 casos positivos (29,2 por cento). Houve correlação direta com o CAS (clinical activity score) elevado em todos os casos e em que consideramos CAS apenas acima de 5, em 54,5 por cento. FGF: Houve expressão em 5 casos (20,8 por cento) com relação direta com CAS elevado em todos os casos e em que consideramos CAS maior que 5 (45,4 por cento). VEGF: Houve dois casos positivos (8,3 por cento) para VEGF nas células endoteliais e estes casos também apresentavam CAS maior que 5. A imunorreatividade foi negativa em todo grupo controle. CONCLUSÃO: Todos os pacientes, com exceção de um, com expressão positiva para FGF, IGF-1 e VEGF mostraram CAS maior que 5, sugerindo importante papel destes fatores de crescimento na patogênese e gravidade da oftalmopatia de Graves. Entretanto, a análise estatística demonstrou associação significativa entre IGF-1 e o sexo masculino (P=0,034). Baixa refletividade ao ultra-som e condição endócrina não estiveram correlacionadas.
Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Tejido Conectivo/metabolismo , Factores de Crecimiento de Fibroblastos/análisis , Oftalmopatía de Graves/metabolismo , Factor I del Crecimiento Similar a la Insulina/análisis , Músculos Oculomotores/metabolismo , Factores de Crecimiento Endotelial Vascular/análisis , Tejido Adiposo/metabolismo , Tejido Adiposo/patología , Biopsia , Estudios de Casos y Controles , Interpretación Estadística de Datos , Oftalmopatía de Graves/etiología , Inmunohistoquímica , Músculos Oculomotores/patología , Estrabismo/metabolismo , Estrabismo/cirugíaRESUMEN
PURPOSE: To descirbe a series of patients in which Thyroid Associated Orbitopathy (TAO) occurred after periocular surgery. METHODS: A retrospective case review of patients who developed TAO in close temporal association with periocular surgical interventions and presented at the orbital clinic from 1997 to 2004. History of previous thyroid abnormality and the lack of TAO signs and symptoms before surgery were reviewed and analyzed. RESULTS: Nine patients that developed TAO in association with periocular surgery were identified. All were women with an average age of 59.3years. (range: 45-75 years). The patients divided into two groups. Group 1 consisted of four patients who had previously been diagnosed with Graves' hyperthyroidism (GH). They ranged in age from 48 to 75 years (average: 58.8 years). The diagnosis of GH had been made an average of 50.5 months (range: 12-96 months) before presentation with TAO. Group 2 consisted of five patients who had no previous history of thyroid abnormality. They ranged in age from 45 to 74 years (average: 60.2 years). No patients had any signs or symptoms of TAO before their recent presentation. CONCLUSIONS: Periocular surgery may lead to local inflammatory events that may contribute to the instigation of TAO in predisposed individuals.