Lymphocytic thrombophilic arteritis: an enigma.

Abstract:

:A 55-year-old woman presented with a 5-year history of livedo racemosa on her limbs. Histology showed vasculitis of medium-sized arteries with a circumferential, hyalinised, intraluminal fibrin ring. Her laboratory investigations did not indicate any underlying systemic disease. The findings were consistent with lymphocytic thrombophilic arteritis (LTA), alias macular arteritis, which is a recently described entity. The importance of LTA lies in the fact that it is a close clinical and microscopic mimic of polyarteritis nodosa (PAN). LTA is believed to be a distinct entity by some and as a form of PAN by others. We have discussed this case in our report.

journal_name

Indian J Dermatol

authors

Kalegowda IY,Tirumalae R,Murthy KS,Rout P

doi

10.4103/0019-5154.139907

subject

Has Abstract

pub_date

2014-09-01 00:00:00

pages

498-501

issue

5

eissn

0019-5154

issn

1998-3611

pii

IJD-59-498

journal_volume

59

pub_type

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