Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Nov;35(11):1367-1370.
doi: 10.1016/j.healun.2016.07.014. Epub 2016 Jul 27.

Microscopic organizing pneumonia and cellular non-specific interstitial pneumonia are widespread in macroscopically normal-appearing lung tissue in idiopathic pulmonary fibrosis

Affiliations

Microscopic organizing pneumonia and cellular non-specific interstitial pneumonia are widespread in macroscopically normal-appearing lung tissue in idiopathic pulmonary fibrosis

Nevins W Todd et al. J Heart Lung Transplant. 2016 Nov.
No abstract available

PubMed Disclaimer

Conflict of interest statement

None of the authors has a financial relationship with a commercial entity that has an interest in the subject of the presented manuscript or other conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Histologic findings from macroscopically normal-appearing tissue from representative patients, with each hematoxylin and eosin horizontal pair representing low and high magnification images from a single patient. Two representative patients are shown in panels A and B and in C and D, with low magnification demonstrating preserved background lung architecture, numerous foci of organizing pneumonia (OP; arrows) but without cellular non-specific interstitial pneumonia (NSIP), and high magnification showing well-formed foci of OP approximately 400 to 1,000 μm in size. A third patient is shown in panels E and F, which demonstrate widespread cellular NSIP, with numerous inflammatory cells within alveolar septae 50 to 100 μm in thickness, and numerous foci of OP (arrows, inset). A fourth patient is shown in panels G and H, which demonstrate widespread cellular NSIP but without identifiable foci of OP. Panels I and J demonstrate intense α-smooth muscle actin staining of two representative foci of OP: panel I from the patient in panels A and B, and panel J from the patient in panels C and D.

References

    1. Travis WD, Costabel U, Hansell DM, et al. ATS/ERS Committee on Idiopathic Interstitial Pneumonias. An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med. 2013;188:733–48. - PMC - PubMed
    1. Leslie KO. Idiopathic pulmonary fibrosis may be a disease of recurrent, tractional injury to the periphery of the aging lung: a unifying hypothesis regarding etiology and pathogenesis. Arch Pathol Lab Med. 2012;136:591–600. - PubMed
    1. Todd NW, Atamas SP, Luzina IG, Galvin JR. Permanent alveolar collapse is the predominant mechanism in idiopathic pulmonary fibrosis. Expert Rev Respir Med. 2015;9:411–8. - PubMed
    1. Strieter RM. Pathogenesis and natural history of usual interstitial pneumonia: the whole story or the last chapter of a long novel. Chest. 2005;128(5 Suppl):526–32S. - PubMed
    1. Flaherty KR, Travis WD, Colby TV, et al. Histopathologic variability in usual and nonspecific interstitial pneumonias. Am J Respir Crit Care Med. 2001;164:1722–7. - PubMed

Publication types