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Table 3 Comparison of pathological findings (grade 0/1/2/3) in patients with SSc-associated ILD

From: Emphysematous change with scleroderma-associated interstitial lung disease: the potential contribution of vasculopathy?

Characteristics

All subjects

Existence of pathological pulmonary emphysema

P value

Yes (p-PE with SSc-ILD)

No

Lung parenchyma lesion

 Cellular infiltration

0/9/9/3

0/8/5/3

0/1/4/0

0.589

 Lymphoid follicle with germinal center

12/7/1/1

10/5/0/1

2/2/1/0

0.349

 Fibrosis

0/2/14/5

0/1/12/3

0/1/2/2

0.728

 Honeycombing

15/5/1/0

12/3/1/0

3/2/0/0

0.601

 Fibroblastic foci

4/16/1/0

3/12/1/0

1/4/0/0

0.781

 Organizing pneumonia (intra-alveolar polyp)

11/8/2/0

8/7/1/0

3/1/1/0

0.927

 Atelectasis (collapse)

0/11/5/5

0/10/4/2

0/1/1/3

0.046*

 Cyst formation

14/5/2/0

11/3/2/0

3/2/0/0

0.882

 Emphysema

5/12/4/0

0/12/4/0

5/0/0/0

< 0.001*

Pulmonary vascular change

 Muscular pulmonary artery

8/7/6/0

4/7/5/0

4/0/1/0

0.105

  < none; grade 0/positive = grade 1–3>

8/13

4/12

4/1

0.047*

 Arteriole <positive>

19 (90.5)

15 (93.8)

4 (80.0)

0.311

 Venule <positive>

18 (85.7)

14 (87.5)

4 (80.0)

> 0.999

 Interlobular vein <positive>

17 (81.0)

14 (87.5)

3 (60.0)

0.228

  1. Data are presented as mean ± SD, unless otherwise stated. SSc systemic sclerosis, ILD interstitial lung disease, p-PE pathological pulmonary emphysema, UIP usual interstitial pneumonia, NSIP nonspecific interstitial pneumonia, DIP desquamative interstitial pneumonia. *P value less than 0.05