Indian Dermatology Online Journal

CASE REPORT
Year
: 2012  |  Volume : 3  |  Issue : 1  |  Page : 21--24

Cutaneous polyarteritis nodosa: A rare isolated cutaneous vasculitis


Praveen Kumar A Subbanna1, Negi Vir Singh2, Rathinam P Swaminathan1 
1 Department of Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India
2 Department of Immunology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India

Correspondence Address:
Praveen Kumar A Subbanna
Department of Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry - 605 006
India

Cutaneous polyarteritis nodosa (CPAN) is a rare form of cutaneous vasculitis that involves small and medium sized arteries of the dermis and subcutaneous tissue without systemic involvement. It presents with tender subcutaneous nodules, digital gangrene, livedo reticularis and subcutaneous ulcerations. The diagnosis is by skin biopsy and characteristic pathologic feature is a leukocytoclastic vasculitis in the small to medium-sized arterioles of the dermis. We report a rare case of benign cutaneous PAN in a 14-year-old girl who presented with history of fever, subcutaneous nodules with cutaneous ulcer and digital gangrene. The skin biopsy showed leukocytoclastic vasculitis with fibrinoid necrosis in the dermal vessels. She received treatment with steroids and lesions resolved completely over a period of month.


How to cite this article:
Subbanna PA, Singh NV, Swaminathan RP. Cutaneous polyarteritis nodosa: A rare isolated cutaneous vasculitis.Indian Dermatol Online J 2012;3:21-24


How to cite this URL:
Subbanna PA, Singh NV, Swaminathan RP. Cutaneous polyarteritis nodosa: A rare isolated cutaneous vasculitis. Indian Dermatol Online J [serial online] 2012 [cited 2021 Sep 25 ];3:21-24
Available from: https://www.idoj.in/article.asp?issn=2229-5178;year=2012;volume=3;issue=1;spage=21;epage=24;aulast=Subbanna;type=0