Eruptive pseudoangiomatosis.
نویسندگان
چکیده
Eruptive pseudoangiomatosis (EPA) is a rare, benign, spontaneously regressing childhood exanthem. The term was recently coined by Prose et al.1 to describe a dermatosis characterized by the sudden onset of a few to several bright red angioma-like papules with a different histopathology from the true angiomas. We describe three patients with the typical lesions of EPA but with some peculiar features not previously described. We discuss the suspected viral aetiology of EPA, and hypothesize a multifactorial aetiopathogenesis.
منابع مشابه
Eruptive pseudoangiomatosis: three cases in Korean middle-aged women.
Sir, Eruptive pseudoangiomatosis (EPA) is a rare, selflimiting exanthem, which is known to occur primarily in children. The first reports on this disease can be traced back to 1969 when Cherry et al. (1) described acute haemangioma-like lesions occurring in children with echovirus infection. No skin biopsies, however, were performed. In 1993, Prose et al. (2) proposed the term ‘eruptive pseudoa...
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INTRODUCTION Eruptive pseudoangiomatosis consists in the acute development of small vascular lesions in the face and extremities that resolve in several weeks without scarring. Lesions are described as 3-4 mm asymptomatic macules and papules with peripheral whitish halo that blanch upon pressure. Initially it was considered a disease limited to children but it has also been described in adults....
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Eruptive pseudoangiomatosis (EPA) is a benign, asymptomatic and self-resolving disorder that is characterized by the sudden appearance of angiomatous-like papules [1, 2] . The consensus that EPA preferentially affects children had not been queried until Navarro et al. [3] reported their first adult case in 2000. We herein report a frequently relapsing adult case that was successfully controlled...
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ورودعنوان ژورنال:
- The British journal of dermatology
دوره 143 2 شماره
صفحات -
تاریخ انتشار 2000