Volume 25, Issue 3 pp. 359-366
ORIGINAL ARTICLE

An extended high-frequency ultrasound protocol for assessing and quantifying of inflammation and fibrosis in localized scleroderma

Irmina Ranosz-Janicka

Corresponding Author

Irmina Ranosz-Janicka

Chair and Department of Dermatology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland

Correspondence

Irmina Ranosz-Janicka, Chair and Department of Dermatology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

Email: [email protected]

Search for more papers by this author
Anna Lis-Święty

Anna Lis-Święty

Chair and Department of Dermatology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland

Search for more papers by this author
Alina Skrzypek-Salamon

Alina Skrzypek-Salamon

Chair and Department of Dermatology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland

Search for more papers by this author
Ligia Brzezińska-Wcisło

Ligia Brzezińska-Wcisło

Chair and Department of Dermatology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland

Search for more papers by this author
First published: 14 January 2019
Citations: 21

Funding information

Supported by Medical University of Silesia: KNW-1-086/K/7/K.

Abstract

Background

Clinical characteristics of the lesions are used to identify activity and damage in localized scleroderma (LoS). For high-frequency ultrasound (HF-US), the features of active lesions were described.

Materials and Methods

Clinical signs of activity and damage in LoS lesions were assessed with the use of Localized Scleroderma Cutaneous Assessment Tool (LoSCAT) and HF-US by two examiners independently. All US images were obtained using a 20 MHz HF-US (DermaLab System, Cortex Technology, Hadsund, Denmark). The dermal thickness (DT) and echogenicity (intensity score, IS) of the LoS lesional dermis were measured in the area of each lesion with the highest score for erythema (ER), skin thickness (ST), and dermal atrophy (DAT). Measurements were compared to the site-matched unaffected skin. The relative difference of DT and IS values was calculated between each lesion and its normal control for comparison among different clinical scores for ER, ST, and DAT.

Results

A total of 92 lesions in 40 adult patients were examined with HF-US. Thirty one lesions were erythematous, 26 were in sclerosis, and 35 were in atrophy. A correlation between the clinical evaluation of the LoS lesions and US measurements was found. The sensitivity and specificity of HF-US were 97% and 90%, respectively. The positive predictive value was 83%, negative predictive value—98%. Interrater reliability was excellent for LoSCAT and HF-US findings.

Conclusion

High-frequency ultrasound allows an accurate assessment of the inflammatory and fibrotic skin lesions in LoS.

CONFLICT OF INTEREST

The authors declare that they have no conflict of interest.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.