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Number of results

Journal

2013 | 8 | 5 | 577-579

Article title

Blue toe syndrome as the initial manifestation of ANCA-associated vasculitis

Content

Title variants

Languages of publication

EN

Abstracts

EN
The blue (or purple) toe syndrome describes the development of a blue or violaceous discoloration in one or more toes in the absence of obvious trauma, serious cold-induced injury or disorders producing generalized cyanosis. The presence of blue toe syndrome requires the clinician to search for primary systemic vasculitides, as well as for malignancy, underlying infection, thrombosis, cardiovascular pathology and other diseases. An accurate diagnosis is critical because many of the causes threaten life or limb, but the patient’s medical history, accompanying non-dermatologic findings on physical examination and the use of discriminatory laboratory tests are usually more important than the nature of the cutaneous abnormalities. We describe the case of a 53-year-old Caucasian male patient presenting with blue toe syndrome as the initial manifestation of ANCA-associated vasculitis.

Publisher

Journal

Year

Volume

8

Issue

5

Pages

577-579

Physical description

Dates

published
1 - 10 - 2013
online
18 - 9 - 2013

Contributors

  • Clinic of Rheumatology, University Hospital St.Ivan Rilsky, Sofia, Bulgaria
  • Department of Clinical Immunology, University Hospital Alexandrovska, 1.G. Sofiiski Str., Sofia, 1431, Bulgaria
author
  • Department of Clinical Immunology, University Hospital Alexandrovska, 1.G. Sofiiski Str., Sofia, 1431, Bulgaria
  • Clinic of Rheumatology, University Hospital St.Ivan Rilsky, Sofia, Bulgaria

References

  • [1] Hirschmann J. V. and Raugi G.J., Blue (or purple) toe syndrome, J. Am. Acad. Dermatol., 2009, 60, 1–20 http://dx.doi.org/10.1016/j.jaad.2008.09.038[Crossref]
  • [2] Hahn B. H., Vasculitis: Attack of the Leukocytes, Lupus News, 2003, 23
  • [3] Pipitone N., Holl-Ulrich K., Gross W.L., Lamprecht P., Unclassified vasculitis with acral ischemic lesions: “form fruste” or idiopathic vasculitis, Clin. Exp. Rheumatol., 2008, 26(3 suppl. 49), S 41–66

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11536-012-0142-5
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