Choi Seung Won, Lew Sogu, Cho Sung Do, Cha Hee Jeong, Eum Eun A, Jung Hyun Chul, Park Jae Hoo
Department of Internal Medicine, Ulsan University Hospital, College of Medicine, University of Ulsan, Dong-gu, Ulsan, Korea.
J Korean Med Sci. 2006 Apr;21(2):371-3. doi: 10.3346/jkms.2006.21.2.371.
Cutaneous polyarteritis nodosa (CPAN) is an uncommon form of vasculitis involving small and medium sized arteries of unknown etiology. The disease can be differentiated from polyarteritis nodosa by its limitation to the skin and lack of progression to visceral involvement. The characteristic manifestations are subcutaneous nodule, livedo reticularis, and ulceration, mostly localized on the lower extremity. Arthralgia, myalgia, peripheral neuropathy, and constitutional symptoms such as fever and malaise may also be present. We describe a 34-yr-old woman presented with severe ischemic change of the fingertip and subcutaneous nodules without systemic manifestations as an unusual initial manifestation of CPAN. Therapy with corticosteroid and alprostadil induce a moderate improvement of skin lesions. However, necrosis of the finger got worse and the finger was amputated.
皮肤型结节性多动脉炎(CPAN)是一种罕见的血管炎形式,累及病因不明的中小动脉。该疾病可因其局限于皮肤且无内脏受累进展而与结节性多动脉炎相鉴别。其特征性表现为皮下结节、网状青斑和溃疡,大多局限于下肢。也可能出现关节痛、肌痛、周围神经病变以及发热和不适等全身症状。我们描述了一名34岁女性,以指尖严重缺血改变和皮下结节为表现,无全身症状,这是CPAN一种不寻常的初始表现。使用皮质类固醇和前列地尔治疗使皮肤病变有中度改善。然而,手指坏死加重,最终手指被截肢。