Best practice & research. Clinical rheumatology
February 27, 2026 · via Europe PMC
Raynaud's phenomenon and digital ulceration in systemic sclerosis.
Turnbull A, Pauling JD.
AI summary — for doctors, generated from the abstract only
Raynaud's phenomenon affects virtually all people with systemic sclerosis and digital ulcers about half, with ulcers reflecting progressive microangiopathy rather than simply severe vasospasm.
What was studied
A chapter review of the burden, pathogenesis, assessment, and management of SSc-related Raynaud's phenomenon and digital ulcers, with clinical examples and reference to recent guidelines.
Key findings
- Immune-mediated endothelial injury and obliterative microangiopathy are key drivers of SSc
- Digital ulcers develop in around half of patients at some stage
- Ulcers involve more protracted hypoxia and are linked to irreversible capillary loss
- Management discussion includes unlicensed therapies for which the evidence base is sometimes scant
Clinical relevance
The review offers practical guidance on assessing and managing digital vasculopathy in SSc, while acknowledging limited evidence for some therapies.
Who should care
Limitations
Not assessable from the abstract alone.
Digital vascular complications in systemic sclerosis are complex and require nuanced, guideline-informed management.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Systemic sclerosis (SSc) is a vascular disease. Immune-mediated endothelial injury leading to vasculopathy characterised by a progressive obliterative microangiopathy is a key aetiopathogenic driver of SSc. This typically manifests clinically as Raynaud's phenomenon (RP), which occurs in virtually all individuals with SSc and digital ulcers (DU), which develop in around half of patients at some stage in the disease course. The term RP encompasses a constellation of clinical features associated with digital vasospasm, typically in response to cold exposure. People with SSc-DU typically report more severe RP symptoms but it is an over-simplification to suggest that DU are simply a consequence of profound RP. The level of ischaemic tissue injury required to cause DU requires more protracted tissue hypoxia and there is a large body of work linking SSc-DU disease with progression of the obliterative microangiopathy and irreversible capillary loss typical of established SSc. The present chapter shall discuss the burden, aetiopathogenesis, assessment and management of SSc-RP and SSc-DU. We shall highlight practical considerations for the assessment and management of these digital vascular complications in routine clinical practice. The complexity of SSc-related digital vasculopathy is illustrated through examples from the clinic setting. The management of these complications shall focus on recently published clinical guidelines, highlighting nuances of management and the therapeutic rationale underpinning the use of unlicensed therapies for which the evidence base is sometimes scant.
DOI
10.1016/j.berh.2026.102121
PMID
41760496
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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