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2016, Número 1

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Neumol Cir Torax 2016; 75 (1)


Primer Consenso Mexicano sobre Fibrosis Pulmonar Idiopática

Mejía M, Buendía-Roldan I, Mateos-Toledo H, Estrada A, Espinoza-Hernández M, Juárez-Hernández F, Vargas-Domínguez C, Selman M

Idioma: Español
Referencias bibliográficas: 96
Paginas: 32-51
Archivo PDF: 1826.33 Kb.


FRAGMENTO

La enfermedad pulmonar intersticial (EPI) en ausencia de algún proceso infeccioso y/o neoplásico engloba varios trastornos respiratorios, los cuales tienen presentación clínica variable (aguda, subaguda o crónica). Debido a que son entidades con histologías diferentes, cursan con diferentes grados de inflamación y fibrosis que al progresar muestran rasgos cicatrizales variables donde el pulmón terminal es el resultado final de esta progresión, perdiendo sus características específicas, lo que imposibilita diferenciarlas en forma adecuada.


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