Alquorain Nada Abdulaziz A, Aljabr Abdullah Salih H, Alghamdi Nada Juman
Department of Dermatology, King Fahd Hospital of the University, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Saudi J Med Med Sci. 2018 May-Aug;6(2):104-107. doi: 10.4103/sjmms.sjmms_148_16. Epub 2018 Apr 16.
Cutaneous polyarteritis nodosa is a rare type of cutaneous vasculitis. It affects the small- and medium-sized arteries of the dermis and subcutaneous tissue without extracutaneous involvement. The diagnosis is by skin biopsy, and the characteristic finding is a leukocytoclastic vasculitis. We report a case of a 14-year-old Saudi girl who was referred to the dermatology service because of multiple ulceronecrotic lesions on the frontal aspects of the distal lower limbs. She had past medical consultations and treatment but without improvement. The histopathology confirmed the clinical diagnosis of cPAN, and ultimately, she responded to treatment with pentoxifylline and topical clobetasol propionate. It is important to be aware of this disease and refer the patient to the dermatology service for the appropriate evaluation and treatment.
皮肤型结节性多动脉炎是一种罕见的皮肤血管炎。它累及真皮和皮下组织的中小动脉,不累及皮肤外组织。诊断依靠皮肤活检,特征性表现为白细胞破碎性血管炎。我们报告一例14岁沙特女孩,因双下肢远端前部多发溃疡坏死性皮损转诊至皮肤科。她曾接受过多次医学咨询和治疗,但均无改善。组织病理学证实了临床诊断为皮肤型结节性多动脉炎,最终,她对己酮可可碱和外用丙酸氯倍他索治疗有反应。认识到这种疾病并将患者转诊至皮肤科进行适当评估和治疗很重要。