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Updated: Jun 21, 2026

Measurement of the Pressure-volume Curve in Mouse Lungs
Published on: January 27, 2015
[Functional respiratory evolution in two patients with emphysema and pulmonary fibrosis]
Santiago C Arce1, Luciana Molinari, Eduardo L De Vito
1Servicio de Neumonología y Laboratorio Pulmonar, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires, Argentina. arcesantiago@fibertel.com.ar
Abstract:
Combined pulmonary fibrosis and emphysema (CPFE) is a frequently under-diagnosed condition. Isolated pulmonary function tests (PFT) can give rise to misinterpretations. We have found no reports on these patients' spirometric progression. We describe two cases of CPFE, showing long-term functional evolution to have a more accurate understanding of current spirometric values. The most relevant findings are: 1) spirometry with discrete functional alterations in the presence of a marked dyspnea and the need, in one patient, for chronic oxygen therapy; and 2) functional evolution reflecting "pseudonormalisation" of the initial obstructive spirometric pattern, possibly as a result of fibrosis development. A mild obstructive defect in a patient with chronic airflow limitation and marked impairment of his/her clinical status and functional class should alert on the possibility of associated pulmonary fibrosis. A computed tomography (CT) and previous PFTs will allow a better understanding of this condition.
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