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Published on: June 16, 2020
Dynamics of digital ulcers in systemic sclerosis
Carmen Bobeică1,2, Alin Laurențiu Tatu3,4, Mihaela Crăescu2,5
1Department of Dermato-Venereology, Doctoral School, University of Medicine and Pharmacy 'Gr. T. Popa' Iaşi, 700115 Iaşi, Romania.
Abstract:
Systemic sclerosis (SSc) is a collagenosis with insufficiently known etiopathogenesis, characterized by microvasculopathy and excessive fibrosis in the context of an autoimmune disorder. The incompletely elucidated pathogenesis and limited therapeutic options, disabling aspects, skin lesions and pain determine important functional and psychological deficiencies which affect the quality of life. It is imperative to observe and correlate individual clinical and paraclinical data to optimize disease management. A group of 22 patients diagnosed with SSc, hospitalized in a university clinic in Bucharest was included in an observational study. The evolution of digital ulcers was evaluated as an indicator of vasculopathy and their status and dynamics were correlated with clinical elements reflecting the fibrotic aspect of the disease. The present study shows that the Raynaud phenomenon is almost always present during the course of the disease, but its presence is not always associated with digital ulcers. The existing data in the literature show that fibrosis is subsequent to vasculopathy, but this study did not reveal causality between these two aspects of pathogenesis. The presence of microstomia and digital contracture was identified in the presence of digital ulcers, but also in their absence. The etiopathogenic mechanisms with multiple unknown involved factors open the opportunity to investigate many aspects of SSc for optimal aiming of therapeutic interventions.
Insights
Systemic sclerosis (SSc) involves vasculopathy and fibrosis, impacting quality of life. This study observed digital ulcers and fibrotic signs in 22 SSc patients, finding no direct causality between these aspects.
Area of Science:
- Rheumatology
- Immunology
- Dermatology
Background:
- Systemic sclerosis (SSc) is a complex autoimmune disease with poorly understood origins.
- It features microvasculopathy, excessive fibrosis, and significant impacts on patient quality of life.
- Limited therapeutic options necessitate a deeper understanding of SSc pathogenesis.
Purpose of the Study:
- To investigate the relationship between vasculopathy (digital ulcers) and fibrosis in Systemic sclerosis.
- To correlate clinical and paraclinical data for improved disease management.
- To explore the interplay of Raynaud phenomenon, microstomia, and digital contractures with disease manifestations.
Main Methods:
- An observational study involving 22 hospitalized Systemic sclerosis patients.
- Evaluation of digital ulcer evolution as a marker of vasculopathy.
- Correlation of digital ulcer status and dynamics with fibrotic clinical indicators.
Main Results:
- Raynaud phenomenon is nearly universal in SSc but not always linked to digital ulcers.
- No causal link was established between fibrosis and vasculopathy in this cohort.
- Microstomia and digital contractures occurred with and without digital ulcers.
Conclusions:
- The pathogenesis of Systemic sclerosis is multifactorial with many unknown elements.
- Further research is needed to elucidate SSc mechanisms for targeted therapies.
- Observing individual patient data is crucial for optimizing SSc management.
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