A New Clinical Scenario: the Presence of Neutrophil Anti-Cytoplasm Antibodies in the Combination of Pulmonary Fibrosis and Emphysema (CFPE)
Received Date: Jul 23, 2020 / Accepted Date: Aug 06, 2020 / Published Date: Aug 13, 2020
Abstract
Combination of pulmonary fibrosis and emphysema (CFPE) is an entity defined in last years, with tobacco as the main etiological factor. Recent studies have associated it with connective tissue diseases and autoimmunity phenomena. The objective of this case series is to review some key aspects of CFPE from the diagnostic and therapeutic point of view, as well as its association with autoimmune diseases. This is a case series of three patients with CPFE associated with ANCA positive type MPO vasculitis.
We present three elderly male patients with important accumulated tobacco consumption who initially presented non-specific general and pulmonary symptom. They had elevated acute phase reactants and positive ANCA antibodies type MPO in blood. HRCT revealed areas of emphysema in the upper lobes and fibrosis in the lower ones . Initially, both patients presented normal result in spirometry but a marked decrease of DLCO. In the three cases biopsies were compatible with medium-vessel vasculitis. We apply corticosteroids associated with immunosuppressant therapy, obtaining different results in each cases.
Keywords: Emphisema; Fibrosis; Autoimmunity; Neutrophil anti-cytoplasm antibodies
Citation: Garcia-Morillo JS, Alba DB, Suárez SR (2020) A New Clinical Scenario: the Presence of Neutrophil Anti-Cytoplasm Antibodies in the Combination of Pulmonary Fibrosis and Emphysema (CFPE). Diagn Pathol Open 5: 170. Doi: 10.4172/2476-2024.1000170
Copyright: © 2020 Garcia-Morillo JS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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