The usefulness of nailfold capillaroscopy in scleroderma-spectrum disorders: a single-centre observational study.

Postepy Dermatol Alergol

Department of Rheumatology and Systemic Connective Tissue Diseases, Medical University of Lublin, Lublin, Poland.

Published: June 2024

AI Article Synopsis

  • Nail-fold capillaroscopy is a non-invasive technique used to evaluate microcirculation, helping in the diagnosis and treatment monitoring of scleroderma and related diseases.
  • A study of 15 patients with scleroderma-spectrum disorders revealed that mixed systemic connective tissue disease and dermatomyositis were common diagnoses, with distinct capillaroscopic patterns linked to each condition.
  • The findings showed that a decrease in the number of blood vessels was associated with interstitial lung disease, and patients with systemic connective tissue disease had higher rates of Raynaud's phenomenon and arthritis compared to those with dermatomyositis.

Article Abstract

Introduction: Nail-fold capillaroscopy is a non-invasive method for assessment of the microcirculation in nail folds. This examination is particularly useful for diagnosis, assessment of activity, evaluation of the response to treatment, and assessment of the correlation of changes in microvessels with changes in organs in systemic sclerosis and in scleroderma-spectrum diseases, i.e. dermatomyositis, polymyositis, mixed connective tissue disease, and undifferentiated connective tissue disease.

Aim: To perform capillaroscopic analyses of lesions in patients with scleroderma-spectrum diseases and determine the correlation of the capillaroscopic image with organ manifestations and the serological profile.

Material And Methods: The study involved 15 patients with scleroderma-spectrum disorders.

Results: Mixed systemic connective tissue disease was diagnosed in 8 patients, and dermatomyositis was detected in 7 patients. The study assessed the frequency of clinical symptoms, e.g. interstitial lung disease or arthritis, and the presence of ANA antibodies. Scleroderma-like microangiopathy was diagnosed in 47% of patients with scleroderma-spectrum disorders. The early pattern was found in patients with mixed systemic connective tissue disease, whereas dermatomyositis was characterized by the late pattern. Non-specific changes were found in 27% of the patients, and a normal image was observed in 27% of the patients.

Conclusions: The analysis also revealed that the reduced number of vessels correlated with the occurrence of interstitial lung disease, and the incidence of Raynaud's phenomenon and arthritis was statistically significantly higher in patients with systemic connective tissue disease than in those with dermatomyositis.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11253315PMC
http://dx.doi.org/10.5114/ada.2024.141158DOI Listing

Publication Analysis

Top Keywords

connective tissue
20
tissue disease
16
patients scleroderma-spectrum
12
systemic connective
12
scleroderma-spectrum disorders
8
scleroderma-spectrum diseases
8
patients
8
mixed systemic
8
interstitial lung
8
lung disease
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!