Naslov
Very Early Diagnosis of Systemic Sclerosis in Clinical Practice – Case Report and Review of the Literature

Autori
Marković, Ivan ; Ljilja Posavec, Anja ; Morović- Vergles, Jadranka ; Mitrović, Joško

Izvornik
Acta Dermatovenerologica Croatica (1330-027X) 30 (2022), 4; 251-255

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni

Ključne riječi
Systemic sclerosis ; Raynaud phenomenon ; antibodies ; antinuclear

Sažetak
Systemic sclerosis (SSc) is a systemic autoimmune disease characterised by generalized microangiopathy and fibrosis of skin and internal organs. The 2013 American College of Rheumatology (ACR) / European League Against Rheumatism (EULAR) criteria have contributed considerably to classifying patients with SSc in earlier stages, but they still lack sensitivity for a very early stage of the disease. Criteria for a very early diagnosis of SSc (VEDOSS) have been proposed by EULAR Scleroderma Trial and Research group (EUSTAR) which include three red flags: Raynaud’s phenomenon, puffy fingers and antinuclear antibody positivity, plus SSc specific antibodies positivity and/or abnormal nailfold capillaroscopy. We report a case of a 54-year-old female patient with 6-week history of puffy fingers, Raynaud phenomenon and positive antinuclear antibodies. Further workup revealed early pathologic capillary pattern by nailfold capillaroscopy and positive anticentromere antibodies. Screening for internal organ involvement detected no heart, lung, or upper gastrointestinal tract involvement. The patient was started on pentoxifylline with further follow- up. The aim of the implementation of VEDOSS criteria is to diagnose SSc at the earliest possible stage, so that subclinical internal organ involvement could be detected and appropriate treatment started at a potentially reversible stage

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti

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