https://doi.org/10.4081/reumatismo.2018.1105
Nailfold videocapillaroscopy in antisynthetase syndrome
Accepted: 15 January 2018
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
A 57-year-old woman with a diagnosis of antisynthetase syndrome (ASSD) underwent a nailfold videocapillaroscopy (NVC) showing a scleroderma pattern. Alterations in capillary morphology have been reported in adults with inflammatory myositis (IM) but only recently have the differences in NVC findings between these two diseases been established. ASSD is currently classified as a subset of IM, for which reason only a few studies in literature evaluate its specific hallmarks, showing nonspecific features of NVC in patients with polymyositis and dermatomyositis (DM) and antisynthetase antibodies. To our knowledge, this is the first description of ASSD capillaroscopy features, and the first report of NVC in ASSD with evidence of scleroderma pattern. Further studies are needed to define clearly frequency, typical features, and possible correlation with clinical and serological data of NVC changes in ASSD, differences between microangiopathy in ASSD and systemic sclerosis or DM.
How to Cite
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.
Similar Articles
- P. Grypiotis, A. Ruffatti, M. Tonello, C. Winzler, C. Radu, S. Zampieri, M. Favaro, A. Calligaro, S. Todesco, Clinical significance of fluoroscopic patterns specific for the mitotic spindle in patients with reumatic diseases , Reumatismo: Vol. 54 No. 3 (2002)
- C. Baldini, A. Tavoni, G. Merlini, M. Sebastiani, S. Bombardieri, Primary Sjogren’s syndrome: clinical and serological feature of a single centre , Reumatismo: Vol. 57 No. 4 (2005)
- V. Pengo, A. Ruffatti, Laboratory diagnosis of antiphospholipid syndrome , Reumatismo: Vol. 59 No. 3 (2007)
- P. Sarzi-Puttini, F. Atzeni, F. Salaffi, Pain in rheumatic diseases: how relevant is it? , Reumatismo: Vol. 66 No. 1 (2014)
- S. Tanwar, B. Mattoo, U. Kumar, R. Dada, R. Bhatia, Does human serotonin-1A receptor polymorphism (rs6295) code for pain and associated symptoms in fibromyalgia syndrome? , Reumatismo: Vol. 73 No. 1 (2021)
- M. Fabris, L. Quartuccio, V. De Re, G. Pozzato, C. Mazzaro, A. Tavoni, C. Ferri, S. Salvin, A. Lerussi, C. Fabro, S. Bombardieri, S. De Vita, Fibronectin gene polymorphisms and clinical manifestations of mixed cryoglobulinemic syndrome: increased risk of lymphoma associated to MspI DD and HaeIII AA genotypes , Reumatismo: Vol. 60 No. 1 (2008)
- P. Lazzarin, E. Presotto, A. Polo, Churg-Strauss syndrome presenting as polymiositis: report of a case , Reumatismo: Vol. 61 No. 2 (2009)
- A. Scanu, F. Oliviero, R. Luisetto, P. Sfriso, J.M Dayer, D. Burger, L. Punzi, HDL inhibit cytokine production in a mouse model of urate crystal-induced inflammation , Reumatismo: Vol. 62 No. 4 (2010)
- B. Gharib, A. Ghareh Zadeh Shirazi, E. Moradi, B. Yaghmaei, V. Ziaee, A rare disease with a rare presentation: hemi-atrophy caused by fibromuscular dysplasia in a 27 month old girl , Reumatismo: Vol. 71 No. 1 (2019)
- M.E. Tezcan, B. Isci, Pulmonary multiple cystic lesions in a patient with Behçet’s syndrome , Reumatismo: Vol. 71 No. 2 (2019)
<< < 18 19 20 21 22 23 24 25 26 27 > >>
You may also start an advanced similarity search for this article.
