Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 11 de 11
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Acta Ortop Mex ; 30(4): 196-200, 2016.
Artigo em Espanhol | MEDLINE | ID: mdl-28267910

RESUMO

BACKGROUND: The non-lethal variant of the Escobar or multiple pterygium syndrome is an entity of autosomal recessive inheritance linked to the X chromosome; it is characterized by multiple pterygia (hence its name) located mainly in the neck (95%) and armpits (55%), as well as other orthopedic malformations such as a vertical talus, congenital hip dislocation, and congenital scoliosis. OBJECTIVE: To present an optional surgical technique for the management of severe spinal deformities. CASE REPORT: Twelve-year-old female diagnosed with Escobar syndrome with severe scoliosis which conditions malformations of the chest with lung involvement, producing mechanical ventilatory restriction and increasing the risk of severe lower respiratory tract infection. We performed a hands-free posterior instrumentation with PASS LP system and Smith-Petersen osteotomies. CONCLUSIONS: The Cobb angle improved from 62° to 23° and the sagittal balance from 125 mm to 73 mm.


El síndrome de Escobar o de pterigium múltiple en su variante no letal es una entidad con tipo de herencia autosómica recesiva ligada al cromosoma X; se caracteriza por presentar múltiples pterigiones de ahí su nombre, principalmente localizados en cuello (95%) y axilas (55%), así como otras malformaciones de tipo ortopédico como astrágalo vertical, luxación congénita de cadera y escoliosis congénita.


Assuntos
Anormalidades Múltiplas , Hipertermia Maligna , Escoliose , Anormalidades da Pele , Fusão Vertebral , Criança , Feminino , Humanos , Hipertermia Maligna/complicações , Escoliose/etiologia , Escoliose/cirurgia , Anormalidades da Pele/complicações , Resultado do Tratamento
5.
An Med Interna ; 14(12): 611-4, 1997 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-9580046

RESUMO

STUDY OBJECTIVE: To assess adrenal function in patients with acute pleuropulmonary tuberculosis (APT) and compare it with that function in patients with community-acquired pneumonia (CAP). PATIENTS: Over a period of 6 months all consecutive patients 18 years of age or older with newly diagnosed APT and CAP were entered into the study. MEASUREMENTS: The whole patients had the following investigations: 1) Serum Na+, K+ and glucose concentrations 2) Systolic and diastolic blood pressures. 3) An ultrasonographic study of the adrenal glands. 4) A standard ACTH stimulation test. RESULTS: There was no significative difference in the serum cortisol level between the two groups at any time of the ACTH stimulation test (basal, 30 and 60 minutes), neither when taking into account the increments between basal and 60 minutes after stimulation serum cortisol levels. All patients in both groups had normal ACTH stimulation test with a peak stimulated cortisol level at 60 minutes > 504 nmol/L. CONCLUSIONS: We did not find evidence of adrenal cortical dysfunction in patients with acute pleuropulmonary tuberculosis or with community-acquired pneumonia in our hospital.


Assuntos
Córtex Suprarrenal/fisiopatologia , Tuberculose Pulmonar/fisiopatologia , Glândulas Suprarrenais/diagnóstico por imagem , Hormônio Adrenocorticotrópico , Adulto , Idoso , Idoso de 80 Anos ou mais , Glicemia/análise , Pressão Sanguínea , Infecções Comunitárias Adquiridas , Interpretação Estatística de Dados , Feminino , Humanos , Hidrocortisona/sangue , Masculino , Pessoa de Meia-Idade , Pneumonia/sangue , Pneumonia/fisiopatologia , Estudos Prospectivos , Fatores de Tempo , Tuberculose Pulmonar/sangue , Ultrassonografia
8.
Gastroenterol Hepatol ; 19(4): 210-2, 1996 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-8665361

RESUMO

Ascariasis is one of the most frequent helminthic diseases in man. Most cases follow a subclinical form but may show symptoms related to pulmonary hypersensitivity or digestive complications. Although biliopancreatic complications have been widely described in endemic areas, references in Western countries are scarce. The authors therefore report their experience in 3 cases of this infrequent disease which were recently attended in their hospital over a brief period of time.


Assuntos
Ascaríase , Ascaris lumbricoides , Doenças Biliares/parasitologia , Pancreatopatias/parasitologia , Adulto , Idoso , Animais , Ascaríase/diagnóstico por imagem , Ascaríase/epidemiologia , Doenças Biliares/diagnóstico por imagem , Feminino , Humanos , Pessoa de Meia-Idade , Pancreatopatias/diagnóstico por imagem , Espanha/epidemiologia , Ultrassonografia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA