LAUSR

Abstract: Medical doctors frequently get patients with Raynaud's phenomenon (RP), a frequent symptom in the general population, referred. The importance of distinguishing normal capillaroscopic findings from (pathognomonic) abnormal (pathological) findings (scleroderma pattern), lies in the fact that this distinction allows the differentiation between a primary RP (not connected to any connective tissue disease [CTD]) from a secondary RP due to systemic sclerosis (SSc) and diseases of the scleroderma spectrum. What is normal in primary RP? A normal capillaroscopic pattern, by qualitative assessment, is characterized by a homogeneous distribution of hairpin shaped capillaries as a "comb-like structure", with a density of >7capillaries per mm, with a normal dimension and absence of large hemorrhages Yet, there exists a wide intra- and inter- individual variety in a normal population which will be discussed in this session. What is pathognomonic abnormal in patients with RP due to SSc? Patients with the RP who have an underlying clinically recognizable (= with skin involvement) SSc show a very characteristic combination of capillary abnormalities in the nailfold, which can easily be assessed through qualitative assessment (= pattern recognition). Maricq et al. described last century, with the widefield technique (magnification X12–14) the scleroderma pattern. This pathognomonic combination contains the following: a striking widening of all three segments of the capillary loop (arterial, venous and intermediate), loss of capillaries and disorganization of the nailfold capillary bed. Many branched "bushy" capillaries may also be observed. In 2000, Cutolo et al. qualitatively assessed the nailfolds of an SSc cohort with patients fulfilling the American College of Rheumatology (ACR) criteria for SSc with the nailfold videocapillaroscopic (NVC) technique (magnification X200). According to the different proportions of the hallmark parameters of the scleroderma pattern (giants, capillary loss, hemorrhages and abnormal shapes: (neo)angiogenesis, Cutolo et al. defined three patterns "early", "active" and "late". The central role of capillaroscopy in distinction between a primary and secondary RP due to SSc is reflected by the fact that capillaroscopy is one of the new ACR/EULAR criteria for classifying a patient as having SSc. In this lecture the standard "FAST TRACK" recognition system of the EULAR Study Group on Microcirculation in Rheumatic Diseases to discern scleroderma patterns from non-scleroderma patterns will be taught to the attendees. Suggested further reading: Smith V, et al. Rheumatology (Oxford). 2016;55(5):883-90. Cutolo M, et al. Rheumatology (Oxford). 2018;57(4):757-759. Cutolo M, et al. Autoimmun Rev. 2018;17(4):344-352. Disclosure of Interests: None declared