Literature DB >> 17116831

Livedoid vasculopathy: further evidence for procoagulant pathogenesis.

Bethany R Hairston1, Mark D P Davis, Mark R Pittelkow, Iftikhar Ahmed.   

Abstract

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.

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Year:  2006        PMID: 17116831     DOI: 10.1001/archderm.142.11.1413

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  21 in total

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2.  Livedoid vasculopathy associated with sickle cell trait: significant improvement on aspirin treatment.

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6.  Vasculitic Diseases and Prothrombotic States Contributing to Delayed Healing In Chronic Wounds.

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8.  Livedoid vasculopathy associated with combined prothrombin G20210A and factor V (Leiden) heterozygosity and MTHFR C677T homozygosity.

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10.  Livedoid vasculopathy associated with peripheral neuropathy: a report of two cases.

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