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Cutaneous Polyarteritis Nodosa Treated with Pentoxifylline and Clobetasol Propionate: A Case Report

机译:己酮可可碱和丙酸氯倍他索治疗皮肤结节性多发性动脉炎:一例报告

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摘要

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.
机译:结节性多发性动脉炎是一种罕见的皮肤血管炎。它会影响真皮和皮下组织的中小动脉,而不会引起皮外侵犯。诊断是通过皮肤活检,特征发现是白细胞碎裂性血管炎。我们报告了一名14岁沙特女孩的病例,该女孩由于下肢远端额叶多处溃疡性坏死病灶而被转诊至皮肤科。她曾经接受过医疗咨询和治疗,但没有改善。组织病理学证实了cPAN的临床诊断,最终,她对己酮可可碱和丙酸氯倍他索局部治疗产生了反应。重要的是要意识到这种疾病,并将患者转至皮肤科服务进行适当的评估和治疗。

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