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BMJ Case Rep ; 17(9)2024 Sep 19.
Artículo en Inglés | MEDLINE | ID: mdl-39304215

RESUMEN

A female of reproductive age presents to the emergency department with progressive dyspnoea due to pneumothorax. She has a history of lymphangioleiomyomatosis (LAM) diagnosed by lung biopsy 15 years ago following incidental finding of pneumothorax. Despite various procedural and medicinal treatments, she continued to have recurrent pneumothorax, with three hospital admissions over the preceding 3 months. LAM is a rare cystic lung disease affecting the lymphatic system, which most commonly affects women of childbearing age. It can be diagnosed via imaging or tissue biopsy (gold standard). Treatment can be difficult, and it often requires highly specialised care by pulmonologists and often confers significant limitations to patients' independence and quality of life. Family physicians are often part of multidisciplinary team to provide care to patients with rare chronic conditions.


Asunto(s)
Linfangioleiomiomatosis , Neumotórax , Recurrencia , Humanos , Linfangioleiomiomatosis/complicaciones , Linfangioleiomiomatosis/diagnóstico , Neumotórax/etiología , Neumotórax/terapia , Femenino , Neoplasias Pulmonares/complicaciones , Adulto , Tomografía Computarizada por Rayos X , Disnea/etiología
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