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Diffuse Lung Disease: Connective Tissue-Associated Interstitial Lung Disease |

Clinical Characteristics of Myeloperoxidase Antineutrophil Cytoplasmic Antibody-Positive Interstitial Pneumonia

Aika Suzuki; Susumu Sakamoto; Yusuke Usui; Keishi Sugino; Kazutoshi Isobe; Yujiro Takai; Sakae Homma
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Toho University Omori Medical Center, Ota-ku, Japan


Copyright 2016, American College of Chest Physicians. All Rights Reserved.


Chest. 2016;150(4_S):478A. doi:10.1016/j.chest.2016.08.492
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SESSION TITLE: Connective Tissue-Associated Interstitial Lung Disease

SESSION TYPE: Original Investigation Poster

PRESENTED ON: Wednesday, October 26, 2016 at 01:30 PM - 02:30 PM

PURPOSE: The aim of this study is to assess the clinical characteristics and outcomes of patients with MPO-ANCA positive interstitial pneumonia (IP).

METHODS: We have conducted a retrospective study of 41 patients (20 males and 21 females ; mean age, 73.0 years) with MPO-ANCA positive IP admitted to our hospital between January 2004 and December 2014. 41 patients were classified into IP with systemic involvement of vasculitis (IP associated with microscopic polyangiitis : MPA-IP) and without other organ involvement (pulmonary limited vasculitis : PLV). The clinical features, chest CT scan images, laboratory findings, pulmonary function tests, and survival between these two groups were compared.

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