Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 29
Filtrar
1.
Artículo en Inglés | MEDLINE | ID: mdl-38780968

RESUMEN

CONTEXT: Thyroid-stimulating hormone (TSH) trajectory classification represents a novel approach to defining the adequacy of levothyroxine (LT4) treatment for hypothyroidism over time. OBJECTIVE: This is a proof of principle study that uses longitudinal clinical data, including thyroid hormone levels from a large prospective study to define classes of TSH trajectories and examine changes in cardiovascular (CV) health markers over the study period. METHODS: Growth mixture modeling (GMM), including latent class growth analysis (LCGA), was used to classify LT4-treated individuals participating in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil) based on serial TSH levels. Repeated measure analyses were then utilized to assess within-class changes in blood pressure, lipid levels, hemoglobin A1c, and CV-related medication utilization. RESULTS: From the 621 LT4-treated study participants, the best-fit GMM approach identified 4 TSH trajectory classes, as defined by their relationship to the normal TSH range: (1) high-high normal TSH, (2) normal TSH, (3) normal to low TSH, and (4) low to normal TSH. Notably, the average baseline LT4 dose was lowest in the high-high normal TSH group (77.7 µg, P < .001). There were no significant differences in CV health markers between the classes at baseline. At least 1 significant difference in CV markers occurred in all classes, highlighted by the low to normal class, in which total and high-density lipoprotein cholesterol, triglycerides, and A1c all increased significantly (P = .049, P < .001, P < .001, and P = .001, respectively). Utilization of antihypertensive, antihyperlipidemic, and antidiabetes medications increased in all classes. CONCLUSION: GMM/LCGA represents a viable approach to define and examine LT4 treatment by TSH trajectory. More comprehensive datasets should allow for more complex trajectory modeling and analysis of clinical outcome differences between trajectory classes.

2.
J Clin Endocrinol Metab ; 109(10): 2504-2512, 2024 Sep 16.
Artículo en Inglés | MEDLINE | ID: mdl-38506164

RESUMEN

CONTEXT: The effectiveness of levothyroxine (LT4) in restoring thyroid hormone (TH) homeostasis, particularly serum thyroxine (T4) and triiodothyronine (T3) levels, remains debatable. OBJECTIVE: This work aimed to assess TH homeostasis in LT4-treated individuals using data from the Longitudinal Study of Adult Health in Brazil (ELSA-Brasil) study. METHODS: The ELSA-Brasil study follows 15 105 adult Brazilians (aged 35-74 years) over 8.2 years (2008-2019) with 3 observation points assessing health parameters including serum thyrotropin (TSH), free T4 (FT4), and free T3 (FT3) levels. We analyzed 186 participants that initiated treatment with LT4 during the study, and 243 individuals continuously treated with LT4 therapy. RESULTS: Initiation of therapy with LT4 resulted in an 11% to 19% decrease in TSH, an approximately 19% increase in FT4, and a 7% reduction in FT3 serum levels (FT3 dropped >10% in ∼40% of the LT4-treated patients). This was associated with an increase in triglyceride levels and utilization of hypolipidemic and antidiabetic medications. Participants continuously treated with LT4 exhibited a stable elevation in serum FT4 and a reduction in serum FT3 and TSH levels. While 115 participants (47.3%) had at least 1 serum FT4 levels above the control reference range (>1.52 ng/dL), 38 participants (15.6%) had at least 1 serum FT3 below the reference range (<0.23 ng/dL). CONCLUSION: The present results challenge the dogma that treatment with LT4 for hypothyroidism restores TH homeostasis in all patients. A substantial number of LT4-treated patients exhibit repeated FT4 and FT3 levels outside the normal reference range, despite normal TSH levels. Further studies are needed to define the clinical implications of these findings.


Asunto(s)
Homeostasis , Hipotiroidismo , Tiroxina , Humanos , Persona de Mediana Edad , Tiroxina/uso terapéutico , Tiroxina/sangre , Tiroxina/administración & dosificación , Femenino , Masculino , Adulto , Homeostasis/efectos de los fármacos , Hipotiroidismo/tratamiento farmacológico , Hipotiroidismo/sangre , Estudios Longitudinales , Anciano , Brasil , Hormonas Tiroideas/sangre , Triyodotironina/sangre , Tirotropina/sangre , Pruebas de Función de la Tiroides , Terapia de Reemplazo de Hormonas/métodos
3.
Arch Endocrinol Metab ; 68: e230375, 2024 Feb 29.
Artículo en Inglés | MEDLINE | ID: mdl-38427812

RESUMEN

Differentiated thyroid carcinoma (DTC) accounts for most cases of thyroid cancer, and the heterogeneity of DTC requires that management decisions be taken by a multidisciplinary team involving endocrinologists, head and neck surgeons, nuclear medicine physicians, pathologists, radiologists, radiation oncologists, and medical oncologists. It is important for nonspecialists to recognize and refer patients with DTC who will benefit from a specialized approach. Recent advances in knowledge and changes in management of DTC call for the need to raise awareness on the part of these nonspecialist physicians, including general endocrinologists and medical oncologists at large. We provide an overview of diagnostic and therapeutic principles in DTC, especially those that bear direct implication on day-to-day management of these patients by generalists. Patients with DTC may be broadly categorized as having localized, locally persistent/recurrent, or metastatic disease. Current recommendations for DTC include a three-tiered system that classifies patients with localized disease into low, intermediate, or high risk of persistent or recurrent disease. Risk stratification should be performed at baseline and repeated on an ongoing basis, depending on clinical evolution. One of the overarching goals in the management of DTC is the need to personalize treatment by tailoring its modality and intensity according to ongoing prognostic stratification, evolving knowledge about the disease, and patient characteristics and preference. In metastatic disease that is refractory to radioactive iodine, thyroid tumors are being reclassified into molecular subtypes that better reflect their biological properties and for which molecular alterations can be targeted with specific agents.


Asunto(s)
Adenocarcinoma , Neoplasias de la Tiroides , Humanos , Neoplasias de la Tiroides/patología , Radioisótopos de Yodo/uso terapéutico , Compuestos de Fenilurea , Pronóstico
4.
Arch. endocrinol. metab. (Online) ; 68: e230375, 2024. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1556947

RESUMEN

ABSTRACT Differentiated thyroid carcinoma (DTC) accounts for most cases of thyroid cancer, and the heterogeneity of DTC requires that management decisions be taken by a multidisciplinary team involving endocrinologists, head and neck surgeons, nuclear medicine physicians, pathologists, radiologists, radiation oncologists, and medical oncologists. It is important for nonspecialists to recognize and refer patients with DTC who will benefit from a specialized approach. Recent advances in knowledge and changes in management of DTC call for the need to raise awareness on the part of these nonspecialist physicians, including general endocrinologists and medical oncologists at large. We provide an overview of diagnostic and therapeutic principles in DTC, especially those that bear direct implication on day-to-day management of these patients by generalists. Patients with DTC may be broadly categorized as having localized, locally persistent/recurrent, or metastatic disease. Current recommendations for DTC include a three-tiered system that classifies patients with localized disease into low, intermediate, or high risk of persistent or recurrent disease. Risk stratification should be performed at baseline and repeated on an ongoing basis, depending on clinical evolution. One of the overarching goals in the management of DTC is the need to personalize treatment by tailoring its modality and intensity according to ongoing prognostic stratification, evolving knowledge about the disease, and patient characteristics and preference. In metastatic disease that is refractory to radioactive iodine, thyroid tumors are being reclassified into molecular subtypes that better reflect their biological properties and for which molecular alterations can be targeted with specific agents.

5.
Case Rep Pediatr ; 2023: 6686511, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37790920

RESUMEN

Background: Ring chromosome 17 syndrome is a rare hereditary disorder whose prevalence is less than 1 : 1.000.000. We present a ten-year-old patient with ring chromosome 17 syndrome who had short stature and was treated with recombinant human growth hormone (rhGH). Case Report. A ten-year-old male scholar had moderate left conductive deafness, left kidney hypoplasia with hypertension, epilepsy, malformations in hands, feet, and abdomen, and disproportionately short stature. Despite no evidence of growth hormone deficiency, rhGH treatment was indicated as a therapeutic test due to his decelerated growth velocity and severe short stature. As a result, his growth velocity increased by 4.2 cm per year and his stature Z-score increased (from -5.87 to -5.23). Conclusion: The patient's severe short stature may be related to genetic, environmental, and hormonal factors and the positive response to rhGH may indicate abnormalities in the somatotropic axis that were mitigated with the treatment. Although rhGH associated with adequate comorbidities controls improved his growth velocity and height Z-score, its effects in the long term are still unclear.

6.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);88(supl.4): S163-S169, Nov.-Dec. 2022. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1420863

RESUMEN

Abstract Objectives: This study aims to investigate if a sampling method using virtual networks is feasible to survey AS adoption among this "hard-to-reach" population of Brazilian doctors. Methods: An online piloted 11-point structured survey questionnaire (designed using Googleforms®) probed the actual treatment patterns for adult patients with PTMCs, including treatment decision-making nonoperative options, was undertaken between 10 November and 30 November 2020. Participants were reached by the mobile phone Application (APP) and a snowball sampling strategy was used to recruit a total of 4783 members (maximum number of potential reach), which is the total of doctors of the all 21 social media WhatsApp® groups. Results: From a total of 4783 members (maximum number of potential reach), there were 657 (13.7%) doctors (actual reach) who clicked the web link of the questionnaire, out of whom 512 (10.7%) fully completed the online survey. Among the survey respondents, 361 were endocrinologists (70.5%) and 151 were surgeons (29.5%). Overall, for low-risk PTMCs in an elderly patient, 118 responders (23%) recommend AS, while 390 (76%) recommend immediate surgery as the management, including lobectomy (18.5%) and Total Thyroidectomy (58.2%). The present responders tended to recommend surgery for PTMCs that were located adjacent to the dorsal surface of the thyroid, were multiple, or raised the size during the follow-up. Conclusion: Using snowball sampling strategy as an innovative route to conduct surveys was feasible and applicable but the rate of response was still very low. Our data also suggests the need to investigate if AS is embraced by Brazilian doctors.

7.
Braz J Otorhinolaryngol ; 88 Suppl 4: S163-S169, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35177356

RESUMEN

OBJECTIVES: This study aims to investigate if a sampling method using virtual networks is feasible to survey AS adoption among this "hard-to-reach" population of Brazilian doctors. METHODS: An online piloted 11-point structured survey questionnaire (designed using Googleforms®) probed the actual treatment patterns for adult patients with PTMCs, including treatment decision-making nonoperative options, was undertaken between 10 November and 30 November 2020. Participants were reached by the mobile phone Application (APP) and a snowball sampling strategy was used to recruit a total of 4783 members (maximum number of potential reach), which is the total of doctors of the all 21 social media WhatsApp® groups. RESULTS: From a total of 4783 members (maximum number of potential reach), there were 657 (13.7%) doctors (actual reach) who clicked the web link of the questionnaire, out of whom 512 (10.7%) fully completed the online survey. Among the survey respondents, 361 were endocrinologists (70.5%) and 151 were surgeons (29.5%). Overall, for low-risk PTMCs in an elderly patient, 118 responders (23%) recommend AS, while 390 (76%) recommend immediate surgery as the management, including lobectomy (18.5%) and Total Thyroidectomy (58.2%). The present responders tended to recommend surgery for PTMCs that were located adjacent to the dorsal surface of the thyroid, were multiple, or raised the size during the follow-up. CONCLUSION: Using snowball sampling strategy as an innovative route to conduct surveys was feasible and applicable but the rate of response was still very low. Our data also suggests the need to investigate if AS is embraced by Brazilian doctors.


Asunto(s)
Neoplasias de la Tiroides , Adulto , Humanos , Anciano , Neoplasias de la Tiroides/cirugía , Espera Vigilante , Tiroidectomía , Brasil
8.
Arch Endocrinol Metab ; 65(5): 625-631, 2021 Oct 29.
Artículo en Inglés | MEDLINE | ID: mdl-34591407

RESUMEN

OBJECTIVE: To analyze the association of clinical, anatomical, and ultrasound (US) characteristics of malignancies in Bethesda III or IV (III-B or IV-B) thyroid nodules. METHODS: The association between malignancies and the following variables were analyzed: III-B or IV-B, age < 55 years and ≥ 55 years, sex, family history of thyroid cancer, history of irradiation, nodule size, and ACR TI-RADS classification in 62 participants who underwent thyroidectomy. RESULTS: Of the 62 participants, 87.1% (54/62) were women, 74.2% were < 55 years old, 95.2% had no family history of thyroid cancer, 56.5% had nodules < 2 cm in size, 62.9% were IV-B, and 69.4% were ACR TI-RADS 4. Thirty-two patients had thyroid carcinoma, and 30 had benign histology. Among all factors associated with malignancy, only ACR TI-RADS 5 classification on US was found to be statistically significant (p = 0.014), while III-B with architectural atypia cytological classification was the only one significantly associated with benign status (p = 0.004). CONCLUSION: Only a high risk of malignancy as assessed using US was able to refine the indication for molecular tests in a group of patients with indeterminate nodules. We found 85% (53/62) of III-B or IV-B thyroid nodules would benefit from available molecular diagnostic tests.


Asunto(s)
Neoplasias de la Tiroides , Nódulo Tiroideo , Femenino , Humanos , Persona de Mediana Edad , Patología Molecular , Estudios Retrospectivos , Neoplasias de la Tiroides/diagnóstico por imagen , Neoplasias de la Tiroides/genética , Nódulo Tiroideo/diagnóstico por imagen , Nódulo Tiroideo/genética , Ultrasonografía
9.
Endocr Relat Cancer ; 28(9): R217-R230, 2021 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-34378152

RESUMEN

Differentiated thyroid carcinoma (DTC) combined with congenital hypothyroidism (CH) is a rare situation, and there is no well-established causal relationship. CH is a common congenital endocrine, while DTC occurring in childhood represents 0.4-3% of all malignancies at this stage of life. The association of CH with DTC could be related to dyshormonogenetic goiter (DHG) or developmental abnormalities. This review will explore the clinical features and the molecular mechanisms potentially associated with the appearance of DTC in CH: sporadic somatic driver mutations, chronic increase of thyroid-stimulating hormone (TSH) levels, higher concentrations of hydrogen peroxide (H2O2), cell division cycle associated 8 (Borelain/CDC8) gene mutations, and in others genes associated with CH - either alone or associated with the mechanisms involved in dyshormonogenesis. There are some pitfalls in the diagnosis of thyroid cancer in patients with CH with nodular goiter, as the proper cytological diagnosis of nodules of patients with dyshormonogenesis might be demanding due to the specific architectural and cytological appearance, which may lead to an erroneous interpretation of malignancy. The purpose of this article is to suggest an analytical framework that embraces the fundamental relationships between the various aspects of CH and CDT. In face of this scenario, the entire genetic and epigenetic context, the complex functioning, and cross talk of cell signaling may determine cellular mechanisms promoting both the maintenance of the differentiated state of the thyroid follicular cell and the disruption of its homeostasis leading to cancer. Whereas, the exact mechanisms for thyroid cancer development in CH remain to be elucidated.


Asunto(s)
Hipotiroidismo Congénito , Neoplasias de la Tiroides , Hipotiroidismo Congénito/diagnóstico , Hipotiroidismo Congénito/genética , Hipotiroidismo Congénito/metabolismo , Humanos , Peróxido de Hidrógeno , Mutación , Neoplasias de la Tiroides/genética
10.
Arch. endocrinol. metab. (Online) ; 65(5): 625-631, 2021. tab
Artículo en Inglés | LILACS | ID: biblio-1345189

RESUMEN

ABSTRACT Objective: To analyze the association of clinical, anatomical, and ultrasound (US) characteristics of malignancies in Bethesda III or IV (III-B or IV-B) thyroid nodules. Subjects and methods: The association between malignancies and the following variables were analyzed: III-B or IV-B, age < 55 years and ≥ 55 years, sex, family history of thyroid cancer, history of irradiation, nodule size, and ACR TI-RADS classification in 62 participants who underwent thyroidectomy. Results: Of the 62 participants, 87.1% (54/62) were women, 74.2% were < 55 years old, 95.2% had no family history of thyroid cancer, 56.5% had nodules < 2 cm in size, 62.9% were IV-B, and 69.4% were ACR TI-RADS 4. Thirty-two patients had thyroid carcinoma, and 30 had benign histology. Among all factors associated with malignancy, only ACR TI-RADS 5 classification on US was found to be statistically significant (p = 0.014), while III-B with architectural atypia cytological classification was the only one significantly associated with benign status (p = 0.004). Conclusion: Only a high risk of malignancy as assessed using US was able to refine the indication for molecular tests in a group of patients with indeterminate nodules. We found 85% (53/62) of III-B or IV-B thyroid nodules would benefit from available molecular diagnostic tests.


Asunto(s)
Humanos , Femenino , Neoplasias de la Tiroides/genética , Neoplasias de la Tiroides/diagnóstico por imagen , Nódulo Tiroideo/genética , Nódulo Tiroideo/diagnóstico por imagen , Estudios Retrospectivos , Ultrasonografía , Patología Molecular , Persona de Mediana Edad
11.
Endocrine ; 61(3): 489-498, 2018 09.
Artículo en Inglés | MEDLINE | ID: mdl-29948935

RESUMEN

PURPOSE: Evaluate the impact of TERTp mutation on the outcomes after initial treatment of 45 patients with thyroid carcinomas derived from follicular cells (TCDFC) with aggressive histology, in which the role of this mutation is not yet well defined. METHODS: Analysis of the presence of TERTp (-124C > T and -146C > T), BRAF (V600E), and NRAS (Q 61R) mutations by Sanger sequencing and analysis of their correlation with the patient's outcomes. RESULTS: Forty-five patients with aggressive histopathologic variants were included in the study. Of these, 68.9% had aggressive variants of papillary thyroid cancer (PTC), 22.2% had poorly differentiated thyroid carcinoma (PDTC)/insular carcinoma, and 8.9% had invasive follicular thyroid cancer (FTC) with Hurthle cell features (Hurthle cell carcinoma). Lymph node metastases were present in 46.7% and distant metastases in 54.6%. The response to the initial therapy was excellent in 45.5% and structurally incomplete in 50%. During the follow-up period (median of 56 months; 5-360 months), 47.7% presented with disease progression and 17.8% experienced disease-related death. In 53.3% of the cases at least one molecular alteration (TERTp in 33.4%, BRAF in 24.5%, RAS in 8.9%) was detected. In the multivariate analysis, TERTp mutation was the factor associated with the highest risk (6 times) of having structural disease after initial therapy (p = 0.01), followed by vascular invasion (p = 0.02), gross extrathyroidal extension (ETE) (p = 0.02) and distant metastasis (p = 0.04). Regarding mutational status, only TERTp mutation was associated with disease progression, and diminished disease progression-free survival (PFS). The presence of distant metastasis, vascular invasion and gross ETE were significantly associated with the risk of disease progression. CONCLUSIONS: TERTp mutation appears be an indicator of both persistence and progression of structural disease after initial therapy in aggressive variants of TCDFC, and associates with a shorter progression free survival regardless of the therapy employed.


Asunto(s)
Adenocarcinoma Folicular/genética , Mutación , Telomerasa/genética , Neoplasias de la Tiroides/genética , Adenocarcinoma Folicular/mortalidad , Adenocarcinoma Folicular/patología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Progresión de la Enfermedad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Supervivencia sin Progresión , Regiones Promotoras Genéticas , Neoplasias de la Tiroides/mortalidad , Neoplasias de la Tiroides/patología , Factores de Tiempo , Adulto Joven
12.
Case Rep Endocrinol ; 2017: 8541078, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28270939

RESUMEN

Thyroglossal duct cyst (TDC) is a cystic expansion of a remnant of the thyroglossal duct tract. Carcinomas in the TDC are extremely rare and are usually an incidental finding after the Sistrunk procedure. In this report, an unusual case of a 36-year-old woman with concurrent papillary thyroid carcinoma arising in the TDC and on the thyroid gland is presented, followed by a discussion of the controversies surrounding the possible origins of a papillary carcinoma in the TDC, as well as the current management options.

13.
Rev. méd. Minas Gerais ; 26: [1-8], jan.-dez. 2016.
Artículo en Portugués | LILACS | ID: biblio-964734

RESUMEN

Introdução: O telemonitoramento aperfeiçoa o controle de doenças crônicas, reduz internações e readmissões hospitalares, possibilita alta mais precoce e aumenta a satisfação do paciente. Objetivo: O estudo objetiva avaliar o impacto de um projeto-piloto de telemonitoramento nos valores da hemoglobina glicada (HbA1C) de pacientes portadores de diabete melito tipo 2 (DM2) com controle glicêmico insatisfatório. Busca, ainda, avaliar a viabilidade dessa ferramenta na Atenção Primária, em relação ao uso e à qualidade da transmissão dos dados, segundo a percepção dos usuários. Materiais e Métodos: Selecionaram-se 28 pacientes insulinizados, entre 30 a 80 anos, com diagnóstico de DM2, assistidos pela equipe de Saúde da Família de uma Unidade Básica de Saúde, localizada em Belo Horizonte. Os pacientes apresentavam duas medidas de HbA1C >7% realizadas dentro dos últimos 360 dias, sendo a medida mais recente realizada até 30 dias antes do início do estudo. Os pacientes foram alocados aleatoriamente em dois grupos, sendo 15 pacientes em telemonitoramento domiciliar e 13 em acompanhamento tradicional. Mensurações das HbA1C dos pacientes foram coletadas ao início e após 90 dias de seguimento. Não houve perdas ou exclusões de pacientes. Resultados: Após 90 dias de intervenção, verificou-se redução significativa das médias dos valores de HbA1C apenas nos pacientes sob telemonitoramento (IC95%; p<0,01 em Teste T). Conclusão: Esse projeto-piloto sinaliza que o telemonitoramento em DM2 é viável, de fácil execução e tem impacto positivo e significativo na melhoria do controle glicêmico dos pacientes. Estudos com um número maior de pacientes se fazem necessários para corroborar esses achados. (AU)


Introduction: Decades of research has issued a lot of data about the cost effectiveness and efficacy of many telemedicine applications. Telemonitoring improves control of chronic diseases, it reduces the need for hospital care, the hospital readmission rate, and it allows earlier hospital discharge and increases patient satisfaction. Objective: We evaluate the impact of a pilot project on glycemic telemonitoring in type 2 Diabetes (DM2) patients on measures of glycated hemoglobin (HbA1C) and evaluate the viability of telemonitoring, about the use and quality of data transmission, in primary health care. Materials and Methods: We had 28 insulinized patients aged 30-80 years diagnosed with DM2, assisted by a Family Health Unit from Horizonte-Brazil. Those patients had at least two HbA1C> 7% within the 360 days prior to the survey and they were randomly divided into two groups, - 15 patients with home telemonitoring and 13 patients with traditional follow-up. The HbA1c values of patients were collected at the beginning and after 90 days. There were no 'loss to follow-up' or exclusions cases. Results: Comparison between HbA1C means of both groups revealed a statistically significant reduction in HbA1C levels only in telemonitored group (IC95%; p<0,01 t-test). Conclusions: This pilot project indicates that home telemonitoring in DM2 is viable, easy to perform, and it has a positive and significant impact on glycemic control of these patients. Larger studies are required to confirm these statements. (AU)


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Telemedicina , Diabetes Mellitus Tipo 2 , Atención Primaria de Salud , Hemoglobina Glucada , Comportamiento del Uso de la Herramienta
14.
Cytogenet Genome Res ; 150(3-4): 194-207, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-28231576

RESUMEN

Thyroid cancer derived from follicular cells (TCDFC) comprises well-differentiated (papillary and follicular) carcinoma, poorly differentiated carcinoma, and anaplastic carcinoma. Papillary thyroid carcinoma is the most common endocrine cancer, and its incidence is steadily increasing. Lethality and aggressiveness of TCDFC is inversely correlated with differentiation degree. In this review, an emphasis has been put on molecular markers involved in tumorigenesis of thyroid carcinoma with a focus on aggressive histotypes and the role of such biomarkers in predicting thyroid cancer outcome. Genetic rearrangements in TCDFC (RET/PTC, PAX8/PPARG) and mutations in RAS, BRAF, TERT promoter (TERTp), TP53, PIK3CA, and AKT1 are discussed. The majority of the studies to date indicate that TERTp mutations can serve as a marker of more aggressive disease in all the subtypes of thyroid carcinoma, being the best current marker of poor prognosis, due to its independent association with distant metastases and increased disease-specific mortality. Some studies suggested that a more accurate prediction of thyroid cancer outcome may be possible through a more extensive genetic analysis. The same is true concerning the identification of other mutations that are only relatively frequent in advanced tumors (e.g., TP53, PIK3CA, or AKT1). A better understanding of the prognostic role of TERTp mutation (together with additional ones like BRAF, RAS, PIK3CA, AKT1, or TP53) and the clarification of their putative role in fine-needle aspiration biopsies are likely to allow, in the future, an early refinement of the stratification risk in patients with well-differentiated carcinomas. It is worth noting that, as with any categorical staging system, the risk evaluation within each category (low, intermediate, and high) varies depending on the specific clinicopathologic features of individual patients and the specific biological behavior of the tumor. Finally, besides the diagnostic and/or prognostic significance of the above-mentioned mutations, it is crucial to understand that the molecular pathways and epigenetic alterations will likely turn into interesting targets for new therapies.


Asunto(s)
Carcinogénesis/genética , Marcadores Genéticos , Neoplasias de la Tiroides/genética , Humanos , Mutación , Neoplasias de la Tiroides/patología
15.
Artículo en Portugués | LILACS-Express | LILACS | ID: lil-750868

RESUMEN

Introdução: o Programa Nacional de Telessaúde visa à atualização e capacitação dos médicos das Equipes de Saúde da Família por meio de videoconferências (VCs), com potencial impacto na melhoria da atenção à saúde em locais remotos e redução do deslocamento dos pacientes. Ainda, propõe mais interação da atenção primária com centros especializados. Objetivos: apresentação e avaliação do emprego desse sistema de videoconferências, possibilitando melhor planejamento das ações do projeto. Métodos: analisados 916 questionários de avaliação/retroalimentação preenchidos pelos participantes ao término de 84 VCs de Medicina, no período de 2009 até 2013. As VCssão um braço do Projeto Nacional de Telessaúde e alcançam 50 municípios em Minas Gerais, sob a coordenação da FM-UFMG. Elas realizam-se via web, exigindo aparelhagem mínima no centro difusor e receptor. Resultados: no período do estudo, obteve-se média de 12,64 municípios e 19,42 conferencistas por VC. Destes, a média de médicos foi 12,97. Quanto aos parâmetros de qualidade das VC, alcançaram avaliação positiva (?ótimo? ou ?bom?) o som em apenas 62% delas e a qualidade de imagem em 84%. O tema foi considerado ?interessante? ou ?muito interessante? em 98%. Conclusões: as VCs têm se fortalecido como alternativa para instituições educacionais. Porém, a participação de conferencistas e municípios nesse projeto foi aquém da almejada. Análises comparativas com VCs de outras áreas revelam, ainda, reduzida adesão dos médicos. Entre os problemas detectados, especialmente quanto à qualidade do som, a baixa qualidade de internet nos municípios pode ter contribuído para esse resultado.


Introduction: the National Telehealth Program aims at updating and training doctors in the Family Health Teams by means of videoconferencing (VCs), with potential impact on improving the health care in remote locations and reducing the displacement of patients. In addition, it proposes increased primary care interaction with specialized centers. Objectives: presentation and evaluation of the use of the videoconferencing system allowing for better planning of action in the project. Methods: 916 evaluation /feedback questionnaires were analyzed, completed by participants at the end of 84 VCs in Medicine, between 2009 and 2013. The VCs are a branch of the National Telehealth Project and reach 50 municipalities in Minas Gerais under the coordination of the FM-UFMG. They are held via web, requiring minimal equipment in diffuser and receiver centers. Results: in the study period, an average of 12.64 municipalities and 19.42 speakers were identified. Of these, the average number of doctors was 12.97. The quality parameters achieved positive assessment (?great? or ?good?) in just 62% for the sound, and 84% for the image. The theme was considered ?interesting? or ?very interesting? by 98%. Conclusions: the VCs have been strengthened as an alternative to educational institutions. However, the participation of speakers and municipalities in this project was lessthan desired. The comparative analysis of VCs from other areas also reveals a reduced adhesion of doctors. Among the problems detected, especially regarding the sound quality, the low quality of internet connection in the municipalities may have contributed to this result.

17.
Arq Bras Endocrinol Metabol ; 57(4): 312-6, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23828436

RESUMEN

OBJECTIVE: To evaluate the usefulness of preoperative serum calcitonin (sCT) in patients with nodular disease without suspicion of medullary thyroid carcinoma (MTC) in history or cytology. PATIENTS AND METHODS: sCT was measured before thyroidectomy in 494 patients with nodular disease who had no family history of MTC or multiple endocrine neoplasia type 2, and no cytological suspicion of MTC. RESULTS: Basal sCT was < 10 ng/mL in 482 patients and none of them had MTC. One patient with basal sCT > 100 pg/mL had MTC. Among the 11 patients with basal sCT between 10 and 100 pg/mL, MTC was diagnosed in only one. The two patients with MTC were submitted to total thyroidectomy, combined with elective lymph node dissection indicated exclusively based on hypercalcitoninemia, and sCT was undetectable after six months. CONCLUSIONS: Preoperative sCT is useful for the detection of sporadic MTC in patients with nodular disease, even in the absence of suspicious history or cytology.


Asunto(s)
Calcitonina/sangre , Carcinoma Medular/sangre , Neoplasias de la Tiroides/sangre , Nódulo Tiroideo/sangre , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores/sangre , Biopsia con Aguja Fina , Carcinoma Medular/patología , Niño , Femenino , Humanos , Mediciones Luminiscentes/métodos , Masculino , Persona de Mediana Edad , Cuidados Preoperatorios , Neoplasias de la Tiroides/patología , Nódulo Tiroideo/patología , Tiroidectomía/métodos , Adulto Joven
18.
Arq. bras. endocrinol. metab ; Arq. bras. endocrinol. metab;57(4): 312-316, June 2013. tab
Artículo en Inglés | LILACS | ID: lil-678146

RESUMEN

OBJECTIVE: To evaluate the usefulness of preoperative serum calcitonin (sCT) in patients with nodular disease without suspicion of medullary thyroid carcinoma (MTC) in history or cytology. PATIENTS AND METHODS: sCT was measured before thyroidectomy in 494 patients with nodular disease who had no family history of MTC or multiple endocrine neoplasia type 2, and no cytological suspicion of MTC. RESULTS: Basal sCT was < 10 ng/mL in 482 patients and none of them had MTC. One patient with basal sCT > 100 pg/mL had MTC. Among the 11 patients with basal sCT between 10 and 100 pg/mL, MTC was diagnosed in only one. The two patients with MTC were submitted to total thyroidectomy, combined with elective lymph node dissection indicated exclusively based on hypercalcitoninemia, and sCT was undetectable after six months. CONCLUSIONS: Preoperative sCT is useful for the detection of sporadic MTC in patients with nodular disease, even in the absence of suspicious history or cytology.


OBJETIVO: Avaliar a utilidade da calcitonina sérica (sCT) pré-operatória em pacientes com doença nodular sem suspeita de carcinoma medular de tireoide (CMT) pela história e citologia. PACIENTES E MÉTODOS: Antes da tireoidectomia, sCT foi dosada em 494 pacientes com doença nodular, sem história familiar de CMT ou neoplasia endócrina múltipla tipo 2 e sem citologia suspeita para CMT. RESULTADOS: sCT basal foi < 10 ng/ml em 482 pacientes e nenhum possuía CMT. Um paciente com sCT basal > 100 pg/ml realmente possuía CMT. Dos 11 pacientes com sCT basal entre 10 e 100 pg/ml, CMT foi diagnosticado em apenas um. Os dois pacientes com CMT foram submetidos à tireoidectomia total com dissecção eletiva de linfonodos, indicada exclusivamente pela hipercalcitoninemia, e após seis meses apresentaram sCT indetectável. CONCLUSÕES: Em pacientes com doença nodular, mesmo sem história ou citologia suspeitas, a sCT pré-operatória é útil para detecção do CMT esporádico.


Asunto(s)
Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Calcitonina/sangre , Carcinoma Medular/sangre , Neoplasias de la Tiroides/sangre , Nódulo Tiroideo/sangre , Biopsia con Aguja Fina , Biomarcadores/sangre , Carcinoma Medular/patología , Mediciones Luminiscentes/métodos , Cuidados Preoperatorios , Neoplasias de la Tiroides/patología , Nódulo Tiroideo/patología , Tiroidectomía/métodos
19.
Arq Bras Endocrinol Metabol ; 49(2): 323-7, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16184265

RESUMEN

Pituitary duplication is a rare malformation commonly associated with other major neural/craniofacial anomalies, easily shown by magnetic resonance imaging. The authors describe two girls with duplication of the pituitary gland and thickening of the hypothalamus, facial dysmorphism and precocious pubertal development. The pathogenesis of pituitary duplication and its relationship with precocious pubertal development are discussed.


Asunto(s)
Hipófisis/anomalías , Pubertad Precoz/etiología , Niño , Femenino , Humanos , Imagen por Resonancia Magnética , Hipófisis/embriología
20.
Arq. bras. endocrinol. metab ; Arq. bras. endocrinol. metab;49(2): 323-327, abr. 2005. ilus
Artículo en Inglés | LILACS | ID: lil-409741

RESUMEN

Duplicacão pituitária é uma malformacão rara muitas vezes associada a anomalias neurais/craniofaciais, facilmente demonstradas por imagens em ressonância magnética. Os autores descrevem duas criancas do sexo feminino com duplicacão da glândula pituitária e espessamento do hipotálamo, dismorfismo facial e desenvolvimento puberal precoce. Discute-se a etiopatogenia da duplicacão hipofisária e sua relacão com o quadro de puberdade precoce.


Asunto(s)
Niño , Humanos , Femenino , Hipófisis/anomalías , Pubertad Precoz/complicaciones , Imagen por Resonancia Magnética , Hipófisis/embriología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA