Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Haemophilia ; 24(1): 141-148, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29168597

RESUMO

OBJECTIVES: To assess the reliability of the IPSG MRI scale for tibiotalar (TTJ) and subtalar joint (STJ) changes in young haemophilic patients, correlating MRI findings with functional scores and 3D-rearfoot kinematics. METHODS: A total of 37 haemophilic patients underwent bilateral MRI of the footankle, clinical evaluation and quantitative assessment of their 3D-rearfoot kinematics during walking. TTJ and STJ soft tissues were assessed twice along with osteochondral changes by two radiologists using the IPSG MRI scale. Inter- and intra-observer reproducibility of MRI scoring were tested by means of kappa statistics. Correlational analyses were performed between MRI findings and the Haemophilia Joint Health Score 2.1 (HJHS) and 3D-rearfoot kinematic data. RESULTS: The intra-reader reliability of MRI scoring was good to excellent (Kappa: 0.62-1), whereas the inter-reader reliability was moderate to good (Kappa: 0.54-0.79). Weak yet significant correlations were found between the frontal plane rearfoot range of motion (ROM) during loading response of gait and STJ score, as well as between frontal plane rearfoot ROM during the terminal stance phase and the rearfoot osteochondral lesions. CONCLUSION: The IPSG score appears applicable to not only the TTJ but also the STJ. Contrary to TTJ lesions, those of the STJ do not correlate with the HJHS but do with 3D-rearfoot kinematic data.


Assuntos
Hemofilia A/fisiopatologia , Hemofilia B/fisiopatologia , Articulação Talocalcânea/diagnóstico por imagem , Adolescente , Tornozelo/diagnóstico por imagem , Fenômenos Biomecânicos , Criança , Marcha/fisiologia , Hemofilia A/patologia , Hemofilia B/patologia , Humanos , Processamento de Imagem Assistida por Computador , Imageamento por Ressonância Magnética , Masculino , Amplitude de Movimento Articular , Reprodutibilidade dos Testes , Índice de Gravidade de Doença , Adulto Jovem
2.
J Visc Surg ; 156(4): 319-328, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-30922600

RESUMO

Low-Phospholipid Associated Cholelithiasis (LPAC) is a genetic disease responsible for the development of intrahepatic lithiasis. It is associated with a mutation of the ABCB4 gene which codes for protein MDR3, a biliary carrier. As a nosological entity, it is defined by presence of two of the three following criteria: age less than 40 years at onset of biliary symptoms, recurrence of biliary symptoms after cholecystectomy, and intrahepatic hyperechogenic foci detected by ultrasound. While the majority of clinical forms are simple, there also exist complicated forms, involving extended intrahepatic lithiasis and its consequences: lithiasis migration, acute cholangitis, intrahepatic abscess. Chronic evolution can lead to secondary sclerosing cholangitis or secondary biliary cirrhosis. In unusual cases, degeneration into cholangiocarcinoma may occur. Treatment is built around ursodeoxycholic acid, which yields dissolution of biliary calculi. Complicated forms may call for interventional, radiological, endoscopic or surgical treatment. This synthetic review illustrates and summarizes the different aspects of this entity, from simple gallbladder lithiasis to cholangiocarcinoma, as well as secondary biliary cirrhosis requiring liver transplant, on the basis of clinical cases and the iconography of patients treated in our ward.


Assuntos
Subfamília B de Transportador de Cassetes de Ligação de ATP/genética , Colelitíase , Fosfatidilcolinas/deficiência , Adulto , Fatores Etários , Bile/química , Neoplasias dos Ductos Biliares/etiologia , Colagogos e Coleréticos/uso terapêutico , Colangiocarcinoma/etiologia , Colangite/etiologia , Colangite Esclerosante/etiologia , Colecistectomia , Colelitíase/complicações , Colelitíase/diagnóstico , Colelitíase/genética , Colelitíase/terapia , Códon sem Sentido , Diagnóstico Diferencial , Feminino , Cálculos Biliares/diagnóstico , Cálculos Biliares/etiologia , Cálculos Biliares/terapia , Humanos , Litíase/complicações , Litíase/diagnóstico por imagem , Litíase/terapia , Abscesso Hepático/etiologia , Cirrose Hepática Biliar/etiologia , Hepatopatias/complicações , Hepatopatias/diagnóstico por imagem , Hepatopatias/terapia , Mutação , Gravidez , Complicações na Gravidez/etiologia , Recidiva , Síndrome , Ultrassonografia , Ácido Ursodesoxicólico/uso terapêutico
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA