Bonté I, Mahr A, Laroche L, Guillevin L, Robineau M
Department of Dermatology, Avicenne Hospital, Bobigny, France.
Scand J Rheumatol. 2005;34(1):71-3. doi: 10.1080/03009740410011235.
Kawasaki disease (KD) is an acute vasculitis characterized by marked tropism of the coronary vessels. Usually a childhood disease, KD can occasionally be observed in adults. We report a case of adult-onset KD that presented as a prolonged fever of unknown origin with subsequent development of severe vasculitis, manifested by coronary aneurysms and peripheral gangrene of the lower limbs. Therapy with intravenous immunoglobulins, corticosteroids, aspirin, anticoagulants, and prostacyclin analogue resulted in rapid improvement in the patient's condition but he required partial distal amputation for irreversible gangrene. Peripheral ischaemia leading to gangrene is a very rare feature of KD vasculitis with only 19 cases previously published in the Medline-indexed literature. The outcomes of those patients were poor, being either fatal or requiring distal amputation. All prior cases affected young children less than 1 year old and, to the best of our knowledge, the present case is the first description of peripheral gangrene in adult-onset KD.
川崎病(KD)是一种以冠状动脉显著嗜性为特征的急性血管炎。KD通常是一种儿童疾病,但偶尔也可见于成人。我们报告一例成人起病的KD,表现为不明原因的长期发热,随后发展为严重血管炎,表现为冠状动脉瘤和下肢外周坏疽。静脉注射免疫球蛋白、皮质类固醇、阿司匹林、抗凝剂和前列环素类似物治疗使患者病情迅速改善,但由于不可逆的坏疽,他需要进行部分远端截肢。外周缺血导致坏疽是KD血管炎非常罕见的特征,此前在Medline索引文献中仅发表过19例。这些患者的预后很差,要么死亡,要么需要进行远端截肢。所有先前病例均为1岁以下幼儿,据我们所知,本病例是成人起病KD中外周坏疽的首例描述。