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  Vol. 142 No. 11, November 2006 TABLE OF CONTENTS
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Livedoid Vasculopathy

Further Evidence for Procoagulant Pathogenesis

Bethany R. Hairston, MD; Mark D. P. Davis, MD; Mark R. Pittelkow, MD; Iftikhar Ahmed, MD

Arch Dermatol. 2006;142:1413-1418.

Objective  To further characterize the clinical and pathologic features, disease associations, and laboratory abnormalities of livedoid vasculopathy.

Design  Retrospective study of patients identified from our institutional database from January 1, 1990, to December 31, 2000.

Setting  Tertiary care institution.

Patients  Forty-five patients with biopsy-proved livedoid vasculopathy.

Main Outcome Measures  Clinical presentation, histopathologic diagnosis, results of testing for coagulation abnormalities, and assessment of vascular status.

Results  Thirty-two patients (71.1%) were female (mean age, 45 years; age range, 10-85 years). Bilateral lower extremity disease occurred in 36 patients (80.0%), ulceration in 31 (68.9%), and atrophie blanche in 32 (71.1%). In patients tested, transcutaneous oximetry measurements were decreased in 20 (74.1%) of 27, and factor V Leiden mutation (heterozygous) was noted in 2 (22.2%) of 9, decreased activity for protein C or protein S in 2 (13.3%) of 15, prothrombin G20210A gene mutation in 1 (8.3%) of 12, and lupus anticoagulant in 5 (17.9%) of 28. Anticardiolipin antibodies were present in 8 (28.6%) of 28 patients, and elevated homocysteine levels in 3 (14.3%) of 21. Intraluminal thrombosis was observed in 44 (97.8%) of 45 skin biopsy specimens. Direct immunofluorescence disclosed multiple vascular conjugates in 31 (86.1%) of 36 biopsy specimens.

Conclusions  Livedoid vasculopathy was predominantly bilateral, affected the lower extremities, and was associated with ulceration and atrophie blanche. Histologic evidence of intraluminal thrombosis was observed in almost all biopsy specimens reviewed. Laboratory testing revealed numerous heterogeneous coagulation abnormalities, providing further evidence of procoagulant mechanisms.


Author Affiliations: Departments of Dermatology (Drs Hairston, Davis, Pittelkow, and Ahmed) and Laboratory Medicine and Pathology (Dr Ahmed), Mayo Clinic, Rochester, Minn.


RELATED ARTICLES

Livedoid Vasculopathy Associated With Plasminogen Activator Inhibitor-1 Promoter Homozygosity (4G/4G) Treated Successfully With Tissue Plasminogen Activator
April Deng, Christopher D. Gocke, John Hess, Meyer Heyman, Michael Paltiel, and Anthony Gaspari
Arch Dermatol. 2006;142(11):1466-1469.
ABSTRACT | FULL TEXT  

Livedoid Vasculopathy: What It Is and How the Patient Should Be Evaluated and Treated
Jeffrey P. Callen
Arch Dermatol. 2006;142(11):1481-1482.
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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Successful use of rituximab in a patient with recalcitrant livedoid vasculopathy
Zeni et al.
Ann Rheum Dis 2008;67:1055-1056.
FULL TEXT  

Livedoid vasculopathy: what it is and how the patient should be evaluated and treated.
Callen
Arch Dermatol 2006;142:1481-1482.
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