2013
DOI: 10.1055/s-0033-1343293
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Rezidivierende Ulzerationen bei Livedovaskulopathie

Abstract: This case report demonstrates that unusual entities like livedoid vasculopathy should be considered as rare causes for recurrent leg ulcers because different underlying etiologies need different specific treatment strategies. Until now treatment for patients with livedoid vasculopathy has not been standardized but anticoagulative therapy with low-molecular-weight heparin is considered to be one treatment of first choice.

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Cited by 3 publications
(1 citation statement)
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“…Its pathogenesis involves the focal non-inflammatory thrombosis of dermal veins and venulae in the subpapillary vascular plexus [39,40] that can usually be observed in histopathological examinations [41,42]. Other features include epidermal spongiosis or atrophy in the margin area, vessel wall thickening with endothelial proliferation, fibrinoid degeneration, fibrin deposits and fibrin thrombi in the lumen [38,39,[43][44][45][46]. Subintimal hyalinization and the absence of perivascular inflammation are characteristic, even though secondary inflammatory changes may be observed in later stages [38,42,44,47] (see Table 2, Figure 2).…”
Section: Livedoid Vasculopathymentioning
confidence: 99%
“…Its pathogenesis involves the focal non-inflammatory thrombosis of dermal veins and venulae in the subpapillary vascular plexus [39,40] that can usually be observed in histopathological examinations [41,42]. Other features include epidermal spongiosis or atrophy in the margin area, vessel wall thickening with endothelial proliferation, fibrinoid degeneration, fibrin deposits and fibrin thrombi in the lumen [38,39,[43][44][45][46]. Subintimal hyalinization and the absence of perivascular inflammation are characteristic, even though secondary inflammatory changes may be observed in later stages [38,42,44,47] (see Table 2, Figure 2).…”
Section: Livedoid Vasculopathymentioning
confidence: 99%