Lymphocytic Thrombophilic Arteritis: A Review
Sharif Vakili1, John G Zampella2, Shawn G Kwatra1
1From the Department of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD.
Summary
Lymphocytic thrombophilic arteritis (LTA) is a distinct cutaneous arteritis, separate from cutaneous polyarteritis nodosa (cPAN). Current evidence supports LTA as a unique entity, warranting specific recognition and management strategies.
Area of Science:
- Dermatology
- Vascular Pathology
- Rheumatology
Background:
- Lymphocytic thrombophilic arteritis (LTA), previously termed macular lymphocytic arteritis, is a recently identified cutaneous arteritis.
- Limited data exists regarding LTA's demographics, diagnostic evaluation, and treatment protocols.
- Ongoing debate questions whether LTA is a distinct condition or a variant of cutaneous polyarteritis nodosa (cPAN).
Purpose of the Study:
- To systematically review existing literature on LTA.
- To analyze demographic data, histopathology, and treatment outcomes for LTA.
- To clarify controversies surrounding LTA's classification and its relationship with cPAN and systemic PAN.
Main Methods:
- Systematic literature review of published LTA cases.
- Analysis of demographic information, medical history, and histopathological findings.
- Evaluation of treatment management strategies and outcomes.
Main Results:
- Forty detailed cases of LTA were identified and analyzed.
- The findings suggest LTA is a distinct entity, separate from cPAN and systemic PAN.
- The term LTA is recommended to better reflect the condition's pathophysiology.
Conclusions:
- LTA appears to be a distinct cutaneous arteritis, differentiated from cPAN and systemic PAN.
- Continued use of the term LTA is encouraged over macular lymphocytic arteritis.
- Further research is needed to fully elucidate LTA's characteristics and optimal management.
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