Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
Rev Mal Respir ; 40(6): 479-498, 2023 Jun.
Artigo em Francês | MEDLINE | ID: mdl-37059617

RESUMO

Sickle-cell disease is an autosomal recessive genetic disorder of hemoglobin that causes systemic damage. Hypoxia is the main actor of sickle-cell disease. It initiates acutely the pathogenic cascade leading to tissue damages that in turn induce chronic hypoxia. Lung lesions represent the major risk of morbidity and mortality. Management of sickle-cell disease requires a tight collaboration between hematologists, intensivists and chest physicians. Recurrent episodes of thrombosis and hemolysis characterize the disease. New therapeutic protocols, associating hydroxyurea, transfusion program and stem cell transplantation in severe cases allow a prolonged survival until the fifth decade. However, recurrent pain, crisis, frequent hospital admissions due to infection, anemia or acute chest syndrome and chronic complications leading to organ deficiencies degrade the patients' quality of life. In low-income countries where the majority of sickle-cell patients are living, the disease is still associated with a high mortality in childhood. This paper focuses on acute chest syndrome and chronic lung manifestations.


Assuntos
Síndrome Torácica Aguda , Anemia Falciforme , Pneumopatias , Humanos , Síndrome Torácica Aguda/complicações , Síndrome Torácica Aguda/terapia , Qualidade de Vida , Anemia Falciforme/complicações , Anemia Falciforme/terapia , Transfusão de Sangue/métodos , Pneumopatias/complicações , Pulmão
2.
Arch Pediatr ; 23(1): 61-5, 2016 Jan.
Artigo em Francês | MEDLINE | ID: mdl-26552628

RESUMO

Cushing syndrome (CS) is a rare feature of McCune-Albright syndrome. Treatments consist of bilateral adrenalectomy followed by lifelong glucocorticoid and mineralocorticoid treatment. However, cases of spontaneous remission of CS have been reported in the literature. We report a case of McCune-Albright syndrome with CS treated with metyrapone for 30 months with prolonged remission after a 12-year follow-up. Adrenalectomy may be avoided in some cases of CS caused by McCune-Albright syndrome. Metyrapone could be a good alternative to surgical treatment.


Assuntos
Síndrome de Cushing/tratamento farmacológico , Inibidores Enzimáticos/uso terapêutico , Displasia Fibrosa Poliostótica/complicações , Metirapona/uso terapêutico , Criança , Síndrome de Cushing/etiologia , Feminino , Seguimentos , Humanos , Indução de Remissão
3.
Arch Pediatr ; 12(7): 1120-3, 2005 Jul.
Artigo em Francês | MEDLINE | ID: mdl-15964528

RESUMO

UNLABELLED: Cushing's syndrome reveals McCune-Albright syndrome in a minority of patients. Bilateral adrenalectomy is performed on the majority of cases. CASE REPORT: We present a case of McCune-Albright syndrome revealed by a Cushing's syndrome treated by metyrapone. Results were good, after a 4-year follow up. CONCLUSION: Treatment with metyrapone could be recommended, for some patients, in McCune-Albright syndrome with Cushing's syndrome before chirurgical treatment.


Assuntos
Síndrome de Cushing/tratamento farmacológico , Inibidores Enzimáticos/uso terapêutico , Displasia Fibrosa Poliostótica/tratamento farmacológico , Metirapona/uso terapêutico , Hiperplasia Suprarrenal Congênita/complicações , Hiperplasia Suprarrenal Congênita/tratamento farmacológico , Síndrome de Cushing/complicações , Feminino , Displasia Fibrosa Poliostótica/complicações , Humanos , Lactente , Resultado do Tratamento
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA