Pleuropulmonary Pathology of Autoimmune Connective Tissue ... · Autoimmune Connective Tissue...
Transcript of Pleuropulmonary Pathology of Autoimmune Connective Tissue ... · Autoimmune Connective Tissue...
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Pleuropulmonary Pathology of
Autoimmune Connective
Tissue Diseases
Mathieu C. Castonguay, MD, FRCP(C)
AP Divisional Web Conference
November 19, 2013
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I have no relevant actual or potential conflict
of interest in relation to this presentation
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Learning Objectives
At the end of this session, participants will be able to:
– understand the differences between the histologic patterns of pleuropulmonary diseases associated with connective tissue diseases (CTDs)
– distinguish the most frequent forms of interstitial lesions seen in patients with CTDs
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Clinical Background
• CTDs
– group of autoimmune disorders that affect
mainly (but not exclusively) joints and
muscles
• rheumatoid arthritis (RA)
• systemic lupus erythematosus (SLE)
• Sjögren syndrome
• systemic sclerosis (SSc)
• inflammatory myopathies
• systemic vasculitides
• ankylosing spondylitis
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Clinical Background
• CTDs
– diagnosis can be difficult
– ~50% remain “undifferentiated” one year after
presentation
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Clinical Background
• Pulmonary involvement in CTDs
– incidence variable, but increasing
• infection
• drug toxicity
• amyloidosis
• aspiration
• musculoskeletal dysfunction
• neoplasia
• paraneoplastic
– may be secondary
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Clinical Background
• Pulmonary involvement in CTDs
– may be initial CTD presentation
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Clinical Background
• Pulmonary involvement in CTDs
CTD Pulmonary involvement
(%)
RA 40
SLE 50-70
Sjögren 9-75
SSc 40-60
PM/DM 60
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Clinical Background
• Pulmonary involvement in CTDs
– may affect any of the anatomical compartments
• airways
• alveolated parenchyma
• vasculature
• pleura
– reflects clinical presentation
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Anatomic Pulmonary
Compartments
Interlobular septa
Pulmonary lobule
Mills SE, Histology for Pathologists, 3rd Ed, Figure 18-13B
Pleura Airways
Alveolated parenchyma
Vasculature
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Parenchymal lesions
• Overlap with idiopathic lung diseases
Travis WD, et al. Am J Respir Crit Care Med, 2013; 188 (6): 733-48
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Parenchymal lesions
• Usual interstitial pneumonia (UIP)
can be seen with any of the CTDs
most common ILD pattern in RA
often men, smokers
1 - 4% of RA patients
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Parenchymal lesions
• Usual interstitial pneumonia (UIP)
poor prognosis, but better than in patients with
idiopathic UIP
Song JW, et al. Chest, 2009; 136 (1): 23-30
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Parenchymal lesions
• Usual interstitial pneumonia (UIP)
serology recommended to evaluate for the
possibility of associated CTD
RF, anti-cyclic citrullinated peptide, ANA
Raghu G, et al. Am J Respir Crit Care Med, 2011; 183 (6): 788-824
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Right lung (autopsy specimen, sagittal) 59F with RA UIP pattern
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Parenchymal lesions
• Histopathology of UIP
key features
architectural distortion
temporal heterogeneity
spatial heterogeneity
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Parenchymal lesions
• Histopathology of UIP
Clues to CTD association
germinal centres
fewer fibroblast foci
smaller honeycomb spaces
more inflammation
Song JW, et al. Chest, 2009; 136 (1): 23-30
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Parenchymal lesions
• Non-specific interstitial pneumonia (NSIP)
can be seen with any of the CTDs
most common ILD pattern in majority of CTDs
better prognosis than UIP
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Parenchymal lesions
• Non-specific interstitial pneumonia (NSIP)
some routinely perform serology in NSIP
patients to evaluate for CTD association
Kinder BW. Clin Chest Med, 2012; 33 (1): 111-21
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Parenchymal lesions
• Histopathology of NSIP
key features
temporal uniformity
spatial uniformity
relatively preserved architecture
two subtypes: cellular and fibrosing
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Fibrosing NSIP
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Fibrosing NSIP
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Fibrosing NSIP
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Parenchymal lesions
• Organizing pneumonia (OP)
can be seen with any of the CTDs, albeit less
commonly than fibrosing ILD
good prognosis
responds to corticosteroids
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Parenchymal lesions
• Histopathology of OP
key features
intraluminal organizing fibrosis in airspaces
patchy distribution
preserved architecture
mild chronic interstitial inflammation
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Parenchymal lesions
• Diffuse alveolar damage (DAD)
can be seen with any of the CTDs, albeit less
commonly than fibrosing ILD
poor prognosis
may occur alone, or as an acute exacerbation
of pre-existing fibrosing ILD
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Parenchymal lesions
• Histopathology of DAD
key features
diffuse distribution
temporal uniformity
alveolar septal thickening by organizing fibrosis
acute, organizing, and fibrosing phases
hyaline membranes
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Parenchymal lesions
• Lymphoid interstitial pneumonia (LIP)
rarely encountered
several reclassified as cellular NSIP or
lymphoma
classically in Sjögren
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Parenchymal lesions
• Histopathology of LIP
key features
diffuse distribution
non-granulomatous chronic inflammation
alveolar septa predominantly involved
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