Volume 59, Issue 2 pp. e127-e132
Case Report

Three cases of lymphocytic thrombophilic arteritis presenting with an annular eruption

Robert I Kelly

Robert I Kelly

Department of Dermatology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia

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Edmund Wee

Corresponding Author

Edmund Wee

Department of Dermatology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia

Correspondence: Dr Edmund Wee, Department of Dermatology, St Vincent's Hospital Melbourne, 41 Victoria Parade, Fitzroy, VIC 3065, Australia. Email: [email protected]Search for more papers by this author
Chasari Tancharoen

Chasari Tancharoen

Department of Dermatology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia

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Mei M Tam

Mei M Tam

Department of Dermatology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia

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Showan Balta

Showan Balta

Department of Anatomical Pathology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia

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Richard A Williams

Richard A Williams

Department of Anatomical Pathology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia

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First published: 28 July 2017
Citations: 11
Robert I Kelly, FACD. Edmund Wee, MBBS. Chasari Tancharoen, MBBS. Mei M Tam, Showan Balta, MBBS. Richard A Williams, FRCPA.
Conflict of interest: none.

Abstract

We describe three patients who presented with a striking erythematous non-blanching annular eruption and features of lymphocytic thrombophilic arteritis (LTA), with a prominent lymphocytic vasculitis involving deep dermal vessels. Lymphocytic inflammation was also evident in the superficial vessels and one patient had small superficial ulcers over the ankle area resembling livedoid vasculopathy (LV). Multiple biopsies demonstrated a persistent absence of neutrophils in the infiltrate consistent with a lymphocytic process. In addition to highlighting the annular morphology as a novel presentation of LTA, these cases suggest a possible relationship between LV and LTA and support the notion that they are distinct from neutrophilic vasculitides such as cutaneous polyarteritis nodosa.

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