2019
DOI: 10.1111/micc.12440
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Microvascular involvement in systemic sclerosis and systemic lupus erythematosus

Abstract: Microvascular changes play central roles in the pathophysiology of systemic sclerosis (SSc) and systemic lupus erythematosus (SLE), and represent major causes of morbidity and mortality in these patients. Therefore, clinical tools that can assess the microvasculature are of great importance both at the time of diagnosis and follow up of these cases. These tools include capillaroscopy, laser imaging techniques, infrared thermography and iontophoresis. In this review, we examined the clinical manifestations and … Show more

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Cited by 44 publications
(51 citation statements)
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“…Microvascular alteration including occlusive vasculopathy in patients with SLE is an important issue of the disease and a major cause for morbidity and mortality in these patients [ 12 , 13 ]. Involvement of the posterior segment of the eye usually comes along with poor visual outcomes and is indicative of high disease activity [ 14 ].…”
Section: Discussionmentioning
confidence: 99%
“…Microvascular alteration including occlusive vasculopathy in patients with SLE is an important issue of the disease and a major cause for morbidity and mortality in these patients [ 12 , 13 ]. Involvement of the posterior segment of the eye usually comes along with poor visual outcomes and is indicative of high disease activity [ 14 ].…”
Section: Discussionmentioning
confidence: 99%
“…SLE can affect joints, kidneys, serosal membranes, hematological and cardiovascular systems as well as the skin. Cutaneous manifestations include oral ulcers and acute, subacute or chronic lupus rash; LRa is found in 14-48% of patients with SLE [27].…”
Section: Systemic Lupus Erythematosusmentioning
confidence: 99%
“…OCTA bypasses the limitations of other microvascular imaging modalities (nailfold/sublingual capillaroscopy, cutaneous laser Doppler or speckle contrast imaging, renal biopsy, and immunofluorescence) such as nonspecificity, insensitivity, poor reproducibility, speed, lack of quantifiability, and invasiveness. 20 Although more research is needed to elucidate the pattern of SLE retinopathy detectable on OCTA as well as the pathophysiology of this phenomenon, our results provide a starting point for further study and suggest subclinical retinal microvascular pathology is centered in the foveal area and less evident in the parafovea.…”
Section: Discussionmentioning
confidence: 66%