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











Base de dados
Intervalo de ano de publicação
1.
BMJ Case Rep ; 15(5)2022 May 11.
Artigo em Inglês | MEDLINE | ID: mdl-35545311

RESUMO

In this case report, we present a case of a woman in her late 30s who presented with bilateral motor weakness, headache, hyperglycaemia and hypertension. Investigations revealed very high 24-hour urine cortisol of 90 524, ectopic adrenocorticotropic hormone secreting pheochromocytoma, normal metanephrine levels and empty sella, which has never been reported. CT chest and abdomen revealed enlarged left adrenal gland with large necrotic mass 4.7×4.0 cm most likely neoplastic lesion. The patient was cured after surgical removal of the left adrenal mass. Histological examination revealed 3.5×2.5×2 cm mass consistent with pheochromocytoma. After surgery and a short stay in the intensive care unit, the patient started improving and both antihypertensive treatment and insulin injections were withdrawn.


Assuntos
Síndrome de ACTH Ectópico , Neoplasias das Glândulas Suprarrenais , Síndrome de Cushing , Feocromocitoma , Síndrome de ACTH Ectópico/diagnóstico , Síndrome de ACTH Ectópico/etiologia , Neoplasias das Glândulas Suprarrenais/complicações , Neoplasias das Glândulas Suprarrenais/diagnóstico , Neoplasias das Glândulas Suprarrenais/cirurgia , Hormônio Adrenocorticotrópico , Síndrome de Cushing/complicações , Feminino , Humanos , Metanefrina , Feocromocitoma/complicações , Feocromocitoma/diagnóstico , Feocromocitoma/cirurgia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA