Nailfold capillaroscopy findings of interstitial pneumonia with autoimmune features

Sang-Heon Lee; Hong Ki Min; Se-Hee Kim; Young Whan Kim; Kwang Ha Yoo; Hee Joung Kim; In Ae Kim; Hae-Rim Kim

doi:10.3904/kjim.2022.358

Korean J Intern Med > Volume 38(6); 2023 > Article

Lee, Min, Kim, Kim, Yoo, Kim, Kim, and Kim: Nailfold capillaroscopy findings of interstitial pneumonia with autoimmune features

Original Article

Rheumatology

The Korean Journal of Internal Medicine 2023;38(6):903-911.

Published online: July 25, 2023

DOI: https://doi.org/10.3904/kjim.2022.358

Nailfold capillaroscopy findings of interstitial pneumonia with autoimmune features

Sang-Heon Lee¹, Hong Ki Min², Se-Hee Kim^2,³, Young Whan Kim⁴, Kwang Ha Yoo⁴, Hee Joung Kim⁴, In Ae Kim⁵, Hae-Rim Kim¹

¹Division of Rheumatology, Department of Internal Medicine, Research Institute of Medical Science, Konkuk University School of Medicine, Seoul, Korea

²Division of Rheumatology, Department of Internal Medicine, Konkuk University Medical Center, Seoul, Korea

³Department of Rheumatology, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul, Korea

⁴Division of Pulmonary Medicine, Department of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea

⁵Precision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul, Korea

Correspondence to: Hae-Rim Kim, M.D., Ph.D., Department of Rheumatology, Konkuk University Medical Center, 120-1 Neungdong-ro, Gwangjin-gu, Seoul 05030, Korea, Tel: +82-2-2030-7542, Fax: +82-2-2030-7728, E-mail: kimhaerim@kuh.ac.kr, https://orcid.org/0000-0002-1911-6236

Received November 15, 2022 Revised February 7, 2023 Accepted May 18, 2023

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background/Aims

We evaluated nailfold capillaroscopy (NFC) of interstitial pneumonia with autoimmune features (IPAF) and compared it with that of patients with connective tissue disease-interstitial lung disease (CTD-ILD) and idiopathic interstitial pneumonia (IIP).

Methods

Patients with newly diagnosed as ILD were evaluated using NFC. Baseline demographic, clinical, serological, and high-resolution CT findings were collected. NFC was semi-quantitatively scored with six domains ranging from 0 to 18. In addition, the overall patterns (scleroderma/non-scleroderma patterns) were determined.

Results

A total of 81 patients (31 with CTD-ILD, 18 with IPAF, and 32 with IIP) were included. The non-specific interstitial pneumonia pattern was the most common ILD pattern in the CTD-ILD and IPAF groups, whereas the usual interstitial pneumonia pattern was the most common in the IIP group. The semi-quantitative score of the CTD-ILD group was higher than that of the IPAF or IIP groups (5.8 vs 4.2 vs 3.0, p < 0.001, respectively). Giant capillaries and haemorrhages were more frequently present in the CTD-ILD and IPAF groups than in the IIP group. A scleroderma pattern was present in 27.8% of the IPAF group, whereas none of the IIP patients showed a scleroderma pattern.

Conclusions

NFC findings may be useful in classifying patients with ILD into CTD-ILD/IPAF/IIP.

Keywords: Interstitial pneumonia with autoimmune feature; Connective tissue disease; Idiopathic interstitial pneumonia; Nailfold capillary

Graphical abstract

INTRODUCTION

Interstitial lung disease (ILD) is a relatively common pulmonary manifestation in autoimmune diseases [1]. The ILD can be categorized into five subgroups: 1) idiopathic interstitial pneumonia (IIP), 2) connective tissue disease (CTD)-ILD, 3) hypersensitivity pneumonitis, 4) sarcoidosis-related ILD, and 5) other ILD [2]. Treatment options for CTD-ILD differ from those for IIP [3]. The concept of interstitial pneumonia with autoimmune features (IPAF) was introduced by Mosca et al. [4]. Patients with IPAF simultaneously presented with ILD and some autoimmune features but did not fulfil the specific criteria for autoimmune disease. The European Respiratory Society (ERS)/American Thoracic Society (ATS) Task Force on Undifferentiated Forms of Connective Tissue Disease-ILD established classification criteria for IPAF [5]. IPAF is assumed to be a preclinical stage of autoimmune disease that predominantly presents with pulmonary manifestations (ILD) [6].

The classification criteria for systemic sclerosis (SSc) include ILD [7]. Although classification criteria for SSc includes ILD as one item as classification criteria, however, other autoimmune diseases, such as rheumatoid arthritis (RA), inflammatory myositis, primary Sjögren’s syndrome (pSS), and systemic lupus erythematosus (SLE) can also present with ILD [3,8]. Nailfold capillaroscopy (NFC) can detect abnormalities in microcirculation, and abnormal findings of NFC are mainly found in patients with SSc [9]. Semi-quantitative measurement of NFC was introduced by Cutolo, which includes six components (capillary density, dilated capillary, giant capillary, haemorrhage, ramification, and disorganization of the vascular array), and this scoring system was reliable for monitoring microcirculation damage in patients with SSc [9]. Recent classification criteria for SSc suggested abnormal NFC as one of the items in the classification criteria [7], and the European Alliance of Associations for Rheumatology (EULAR) Study Group on Microcirculation in Rheumatic Diseases (EULAR SG MC/RD) established a standardized definition of scleroderma and non-scleroderma patterns of NFC [10]. Patients with Raynaud’s phenomenon (RP) who presented with a scleroderma pattern of NFC showed a likelihood of progression to CTD [11], whereas RP patients without scleroderma pattern in the NFC showed a high predictive value for excluding SSc [12]. One prospective multi-centre study revealed that patients with combination of RP, SSc specific autoantibodies, and puffy fingers had higher risk for progression to SSc [13]. The scleroderma pattern of NFC is not only found in patients with SSc but also in other autoimmune diseases, such as inflammatory myositis and mixed connective tissue disease (MCTD) [14]. Although, previous study evaluated NFC finding in patients with IPAF [15], however, semi-quantitative scoring of NFC in IPAF patients was not assessed, yet.

In the present study, we aimed to measure the semi-quantitative scoring of the NFC in IPAF patients and compare this with patients with CTD-ILD and IIP. Furthermore, the frequency of scleroderma patterns according to the EULAR SG MC/RD in each group was evaluated.

METHODS

Patients and data extraction

Patients with newly found ILD were evaluated with NFC in a single tertiary university-based hospital, Konkuk University Medical Center, from April 2020 to December 2021. The study was conducted by cross-sectional study. The inclusion criteria were as follows: 1) age over 19 years, 2) underwent NFC, and 3) presence of chest computed tomography (CT). The patients who fulfilled specific criteria for autoimmune diseases (SSc, RA, pSS, inflammatory myositis, SLE, MCTD) were grouped as CTD-ILD group [7,16–20]. Patients who did not fulfil specific classification criteria for an autoimmune disease but satisfied the 2015 ERS/ATS criteria were classified into the IPAF group [5]. Patients with ILD who did not have other aetiologies of ILD were classified into the IIP group. This study was conducted following the Declaration of Helsinki and Good Clinical Practice guidelines, and was approved by the Institutional Review Board (IRB) of Konkuk University Medical Center (IRB no: 2020-04-017). Written informed consent was obtained from all participants before enrolment.

IPAF classification criteria component

Patients suspected of having ILD on a plain chest radiograph underwent chest CT to determine the morphologic pattern of ILD and were classified as usual interstitial pneumonia (UIP), nonspecific interstitial pneumonia (NSIP), organizing pneumonia (OP), NSIP + OP, or lymphoid interstitial pneumonia. In the serologic domain, antinuclear antibody (ANA) was evaluated by indirect immunofluorescence staining using the Hep-2 cell line. Rheumatoid factor (RF), anti-citrullinated peptide antibody, anti-double-stranded DNA Ab, anti-Ro/SSA, anti-La/SSB, anti-ribonucleoprotein, anti-Smith, anti-Scl-70, anti-Jo-1, and anti-centromere Abs were measured by ELISA. ANA was considered positive when the ANA titre was ≥ 1:320 with a diffuse, homogeneous, or speckled pattern, or any titre with a nucleolar/centromere pattern. An RF titre more than twice the upper reference range was considered positive. The clinical domains were checked by a trained rheumatologist and recorded in electronic medical records.

Nailfold capillaroscopy

NFC was performed using video capillaroscopy (YP0901, 200× magnification; Starling Force Co., Ltd., Seoul, Korea) in the 2nd to 5th fingers bilaterally of each patient. The semi-quantitative scoring of NFC was calculated by trained a rheumatologist (S.H. Kim) according to Cutolo’s method, which is composed of six components, each of which can range from 0 to 3 (total score ranged from 0 to 18) [9], and an average of eight digits was recorded. In addition, according to the EULAR SG MC/RD fast-track algorithm, the overall pattern of NFC findings was categorized into scleroderma (early, active, or late) or non-scleroderma (normal or non-specific abnormality) [10].

Sample size calculation

The previous study showed that abnormal finding of NFC was found in 10% of IPAF patients, whereas 78% of CTD-ILD patients had NFC abnormality [15]. Assuming alpha 5%, and statistical power (1 − beta) 80%, two-sided testing, and a drop-out rate of 10%, the required number of samples was at least 18 for each group.

Statistical analysis

One-way analysis of variance or Wilcoxon signed-rank test was properly selected for the analysis of continuous variables and then presented as mean ± standard deviation or median with interquartile range. A posthoc analysis was performed using the Bonferroni method. Categorical variables were compared using the chi-squared test or Fisher’s exact test. Statistical significance was set at p < 0.05. All tests were performed using the R software (R for Windows 3.3.2; The R Foundation for Statistical Computing, Vienna, Austria).

RESULTS

Baseline characteristics of enrolled patients

A total of 81 patients (31 with CTD-ILD, 18 with IPAF, and 32 with IIP) were included in the analysis. The inclusion and exclusion criteria are described in Fig. 1. The CTD-ILD group comprised 16 patients with SSc, five patients with pSS, three patients with RA, three patients with inflammatory myositis, two patients with SLE, and two patients with MCTD. The mean age of the CTD-ILD group was significantly lower than those of the IPAF and IIP groups (p < 0.001). The proportion of female patients was significantly higher in the CTD-ILD group (77.4%) than in the IIP group (34.4%), and the IPAF group had a higher proportion of female patients than the IIP group. The most frequent morphological pattern of ILD was NSIP in both the CTD-ILD and IPAF groups, whereas UIP was the most frequent ILD pattern in the IIP group. Among the clinical domains, RP was more frequently present in the CTD-ILD and IPAF groups, and the presence of RP was significantly higher in these two groups than in the IIP group (p < 0.001). The duration of RP was comparable between three groups: 16.2 ± 7.1, 16.4 ± 5.0, and 15.0 months in CTD-ILD, IPAF, and IIP group, respectively (p = 0.980). In addition, inflammatory arthritis/polyarticular morning stiffness and puffy fingers were more frequently observed in the CTD-ILD and IPAF groups than in the IIP group (p = 0.009 and p = 0.020, respectively). In the autoantibody profile, positivity for ANA was the most frequent serologic component in the CTD-ILD and IPAF groups. Furthermore, most of the autoantibodies were more frequently present in the CTD-ILD group. The presence of anti-dsDNA Ab/anti-Ro/SSA/anti-RNP Ab/anti-Scl70 Ab was significantly higher in CTD-ILD than IPAF or IIP groups. Detailed information on the baseline characteristics is summarized in Table 1.

Comparison of NFC finding between CTD-ILD, IPAF, and IIP group

The semiquantitative scores of the NFC in the CTD-ILD, IPAF, and IIP groups were 5.8, 4.2, and 3.0, respectively. The semi-quantitative score of the IPAF group was lower than that of the CTD-ILD group (p = 0.022) but higher than that of the IIP group (p = 0.048). Giant capillaries and haemorrhage of the nailfold showed significant differences between the CTD-ILD, IPAF, and IIP groups (p < 0.001 and p = 0.017, respectively). The giant capillaries were even more abundant in the CTD-ILD group than in the IPAF group (48.4% vs. 16.7%). Giant capillaries and ramifications were not observed in the IIP group. Regarding the EULAR SG MC/RD definition for the overall pattern, 18 patients (58.1%) in the CTD-ILD group and five patients (27.8%) in the IPAF group showed a scleroderma pattern, whereas none of the patients in the IIP group demonstrated a scleroderma pattern. In the IPAF group, two patients (11.1%) showed a UIP pattern in the morphological domain, and these two patients did not show a scleroderma pattern in the NFC. Representative NFC images of the scleroderma pattern in the IPAF group are shown in Fig. 2. All the detailed NFC findings are presented in Table 2. In addition, the clinical, serologic, and morphologic domains of IPAF classification criteria of IPAF patients who had scleroderma pattern in NFC were summarized in Table 3.

DISCUSSION

In the present study, we demonstrated that NFC findings differed among patients with CTD-ILD, IPAF, and IIP. The semiquantitative score increased in the order of CTD-ILD, IPAF, and IIP. Furthermore, some patients with IPAF showed scleroderma patterns in the NFC.

The NFC finding is one of the classification criteria for SSc [7]. Sulli et al. [9] initially demonstrated the usefulness of NFC in diagnosing SSc and defined six components to quantify NFC abnormalities in patients with SSc. The EULAR SG MC/RD established a fast-track algorithm for discriminating NFC findings for scleroderma and non-scleroderma patterns [10]. The aforementioned algorithm simplifies the definition of the scleroderma pattern of NFC by focusing on the density of capillaries, giant capillaries, and abnormal capillary [10]. The presence of scleroderma pattern in NFC has predictive value in diagnosing CTD, whereas the absence of scleroderma pattern in NFC could exclude SSc [11,12]. In addition, NFC findings can predict SSc progression [21]. The classification criteria for IPAF were recently established by the ERS/ATS research group [5], and IPAF was stated with various terms until the establishment of recent classification criteria for IPAF [6,22]. IPAF has intermediate characteristics of IIP and CTD-ILD, and studies showed that 13.5–18.8% of patients with IPAF developed definite CTD [23,24]. Although the follow-up duration was relatively short (mean follow-up duration: 12–45 mo) and only about 13.5–18.8% developed definite CTD, the study showed that IPAF patients should be considered as having a pre-clinical autoimmune disease and emphasized the need to identify predictors of definite CTD [23,24]. In the present study, the scleroderma pattern was predominantly present in the CTD-ILD group, but a scleroderma pattern was also found in 27.8% of patients in the IPAF group. The subgroup of IPAF patients with a scleroderma pattern in the NFC may develop definite CTD.

The treatment targets of IIP and CTD-ILD differ. The treatment target of CTD-ILD is to reduce inflammatory and autoimmune responses [3,25], whereas IIP (especially idiopathic pulmonary fibrosis) aims to attenuate the fibrosis process [26,27]. In addition, the survival rate was better in the CTD-ILD and IPAF groups than IIP group [28]. Therefore, discriminating between CTD-ILD, IPAF, and IIP is important in patients who are initially diagnosed with ILD. Several studies have shown the predictive role of NFC in differentiating CTD-ILD from IIP [11,12,14], and some recommend performing NFC when ILD is initially diagnosed to diagnose underlying CTD [29]. One study compared NFC findings between CTD-ILD, IPAF, and IIP and reported that reduced capillary density, giant capillaries, and microhaemorrhages were associated with CTD-ILD [30]. But, the study was performed using a smartphone dermatoscope [30], which cannot sufficiently magnify the NFC and is only recommended as a screening test [31,32]. The present study compared semiquantitative scores between the CTD-ILD, IPAF, and IIP groups using video capillaroscopy for the first time. We showed that IPAF patients had higher semiquantitative scores of NFC than the IIP group, but lower scores than CTD-ILD patients, which is similar to the fact that IPAF may be the pre-clinical state of CTD.

The present study has several limitations. First, the number of patients included was relatively small. Second, the study was performed in a cross-sectional manner and included only baseline data. Therefore, the predictive or prognostic role of the NFC in IPAF could not be evaluated in the present study. Third, the morphologic pattern of ILD was only assessed using CT, and none of the enrolled patients underwent biopsy confirmation. Fourth, the UIP pattern was predominant in the IIP group, whereas the NSIP pattern was the most common ILD pattern in the CTD-ILD and IPAF groups. This difference could be due to the intrinsic bias that affected the semi-quantitative score of the NFC in the present study.

In conclusion, the NFC finding of IPAF is intermediate between that of CTD-ILD and IIP. In addition, about one-fourth of IPAF patients showed a scleroderma pattern of NFC, which may be a key clue for predicting CTD development in IPAF patients.

KEY MESSAGE

1. Semiquantitative scoring of NFC could aid in differentiating IPAF from IIP.

2. Giant capillary and haemorrhage of NFC are discriminative characteristics between CTD-ILD/IPAF and IIP.

3. Among IPAF patients, 27.8% of them demonstrated scleroderma patterns in NFC.

Notes

Conflicts of interest

The authors disclose no conflicts.

CRedit authorship contributions

Sang-Heon Lee: conceptualization, data curation, methodology; Hong Ki Min: conceptualization, data curation, formal analysis, methodology, visualization, writing - original draft, writing - review & editing; Se Hee Kim: data curation; Young Whan Kim: data curation; Kwang Ha Yoo: data curation; Hee Joung Kim: conceptualization, data curation; In Ae Kim: data curation; Hae-Rim Kim: conceptualization, data curation, funding acquisition, writing - review & editing

Funding

This paper was supported by Konkuk University in 2021.

Figure 1

Flow chart for patient enrolment. CTD, connective tissue disease; ILD, interstitial lung disease; IIP, idiopathic interstitial pneumonia; IPAF, interstitial pneumonia with autoimmune features.

Figure 2

Representative nailfold capillaroscopy findings of scleroderma patterns according to EULAR Study Group on Microcirculation in Rheumatic Diseases in IPAF group. (A) “Active” scleroderma pattern (decreased capillary density: 4 capillaries/1 mm, giant capillary: black arrow) (B) “Late” scleroderma pattern (decreased capillary density: 3 capillaries/1mm, abnormal morphology: black arrowhead). Scale bar = 1 mm.

Table 1

Baseline characteristics of enrolled patients

Variable	CTD-ILD (n = 31)	IPAF (n = 18)	IIP (n = 32)	p value
Sex, female	24 (77.4)^a)	10 (55.6)^b)	11 (34.4)^c)	0.003
Age (yr)	58.3 ± 13.1^a)	69.9 ± 12.3^b)	71.2 ± 8.6^b)	< 0.001
Morphologic domain
ILD pattern^d)	< 0.001
NSIP	22 (71.0)	14 (77.7)	7 (21.9)
NSIP + OP	1 (3.2)	1 (5.6)	1 (3.1)
OP	1 (3.2)	1 (5.6)	0 (0.0)
UIP	7 (22.6)	2 (11.1)	24 (75.0)
LIP	0 (0.0)	0 (0.0)	0 (0.0)
Unexplained pleural effusion or thickening	6 (19.4)	3 (16.7)	8 (25.0)	0.755
Unexplained pericardial effusion or thickening	1 (3.2)	0 (0.0)	0 (0.0)	0.442
Unexplained intrinsic airway disease	0 (0.0)	0 (0.0)	0 (0.0)	> 0.999
Unexplained pulmonary vasculopathy	0 (0.0)	0 (0.0)	0 (0.0)	> 0.999
Clinical domain
Mechanic hands	2 (6.5)	1 (5.6)	0 (0.0)	0.357
Distal digital tip ulceration	0 (0.0)	1 (5.6)	0 (0.0)	0.170
Inflammatory arthritis or polyarticular morning stiffness (≥ 60 min)	8 (25.8)^a)	4 (22.2)^a)	0 (0.0)^b)	0.009
Palmar telangiectasia	1 (3.2)	0 (0.0)	0 (0.0)	0.442
Raynaud’s phenomenon	14 (45.2)^a)	8 (44.4)^a)	1 (3.1)^b)	< 0.001
Puffy finger	7 (22.6)^a)	2 (11.1)^a)	0 (0.0)^b)	0.020
Gottron’s sign	2 (6.5)	1 (5.6)	0 (0.0)	0.357
Serologic domain
Antinuclear Ab	29 (93.5)^a)	9 (50.0)^b)	1 (3.1)^c)	< 0.001
Rheumatoid factor	7 (22.6)	4 (22.2)	1 (3.1)	0.057
Anti-CCP Ab	5 (16.1)	3 (16.7)	1 (3.1)	0.181
Anti-dsDNA Ab	5 (16.1)^a)	0 (0.0)^b)	0 (0.0)^b)	0.014
Anti-Ro/SSA Ab	16 (51.6)^a)	4 (22.2)^b)	0 (0.0)^c)	< 0.001
Anti-La/SSb Ab	3 (9.7)	0 (0.0)	0 (0.0)	0.081
Anti-RNP Ab	4 (12.9)^a)	0 (0.0)^b)	0 (0.0)^b)	0.034
Anti-Smith Ab	2 (6.5)	0 (0.0)	0 (0.0)	0.191
Anti-Scl-70 Ab	11 (35.5)^a)	2 (11.1)^b)	0 (0.0)^c)	0.001
Anti-centromere Ab	5 (16.1)	2 (11.1)	0 (0.0)	0.068
Anti-Jo-1 Ab	2 (6.5)	1 (5.6)	0 (0.0)	0.357

Values are presented as number (%) or mean ± standard deviation.

Ab, antibody; CTD, connective tissue disease; ILD, interstitial lung disease; IIP, idiopathic interstitial pneumonia; IPAF, interstitial pneumonia with autoimmune features; LIP, lymphoid interstitial pneumonia; NSIP, nonspecific interstitial pneumonia; OP, organizing pneumonia; RNP, ribonucleoprotein; UIP, usual interstitial pneumonia.

^a–c) Different letters indicate significant differences between groups.

^d) p value under 0.05 means each group (CTD-ILD, IPAF, and IIP) has different fraction of ILD pattern.

Continuous variables were analysed by one-way analysis of variance or Wilcoxon signed-rank test and categorical variables were analysed by chi-squared test or Fisher’s exact test.

Table 2

Nailfold capillaroscopy findings of enrolled patients

	CTD-ILD (n = 31)	IPAF (n = 18)	IIP (n = 32)	p value
Semiquantitative score of nailfold capillaroscopy (0–18)	5.8 ± 2.5^a)	4.2 ± 1.9^b)	3.0 ± 1.1^c)	< 0.001
Decreased density of capillary	30 (96.8)	17 (94.4)	31 (96.9)	0.895
Presence of dilated capillary (20 μm ≤ apical diameter < 50 μm)	29 (93.5)	17 (94.4)	30 (93.8)	0.992
Presence of giant capillary (50 μm ≥ apical diameter)	15 (48.4)^a)	3 (16.7)^b)	0 (0.0)^c)	< 0.001
Presence of haemorrhage	14 (45.2)^a)	6 (33.3)^a)	4 (12.5)^b)	0.017
Presence of ramification	5 (16.1)	2 (11.1)	0 (0.0)	0.068
Disorganisation of the vascular array	30 (96.8)	17 (94.4)	30 (93.8)	0.850
EULAR Study Group on Microcirculation in Rheumatic Diseases pattern^d)				<0.001
Early scleroderma pattern	4 (12.9)	0 (0.0)	0 (0.0)
Active scleroderma pattern	10 (32.3)^a)	4 (22.2)^a)	0 (0.0)^b)
Late scleroderma pattern	4 (12.9)	1 (5.6)	0 (0.0)
Nonspecific abnormalities	13 (41.9)^a)	13 (72.2)^b)	26 (81.2)^b)
Normal	0 (0.0)^a)	0 (0.0)^a)	6 (18.8)^b)

Values are presented as number (%) or mean ± standard deviation.

CTD, connective tissue disease; ILD, interstitial lung disease; IIP, idiopathic interstitial pneumonia; IPAF, interstitial pneumonia with autoimmune features.

^a–c) Different letters indicate significant differences between groups.

^d) p value under 0.05 means each group (CTD-ILD, IPAF, and IIP) has different fraction of EULAR Study Group on Microcirculation in Rheumatic Diseases pattern.

Continuous variables were analysed by one-way analysis of variance or Wilcoxon signed-rank test and categorical variables were analysed by chi-squared test or Fisher’s exact test.

Table 3

Clinical, serologic, morphologic features of IPAF patients with scleroderma pattern of NFC

Patient	NFC pattern	Clinical domain	Serologic domain	Morphologic domain
1	Active scleroderma pattern		ANA	NSIP
2	Late scleroderma pattern		ANA	NSIP, unexplained pleural effusion
3	Active scleroderma pattern	Gottron’s sign	ANA	OP
4	Active scleroderma pattern		ANA, anti centromere Ab	NSIP
5	Active scleroderma pattern		Anti Ro/SSA Ab	NSIP

ANA, antinuclear antibody; IPAF, interstitial pneumonia with autoimmune features; NFC, nailfold capillaroscopy; NSIP, nonspecific interstitial pneumonia; OP, organizing pneumonia.

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