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白色萎缩。临床诊断与治疗。

Atrophie blanche. Clinical diagnosis and treatment.

作者信息

Elisaf M, Nikou-Stefanaki S, Drosos A A, Moutsopoulos H M

机构信息

Department of Internal Medicine, School of Medicine, University of Ioannina, Greece.

出版信息

Ann Med Interne (Paris). 1991;142(6):415-8.

PMID:1772181
Abstract

In this report, we describe 11 Greek patients with atrophie blanche (AB). All patients had characteristic skin lesions: petechial or purpuric papules or hemorrhagic bullae, that became necrotic and formed ulcers which in turn, became atrophic scars with hyperpigmentation of the surrounding skin. The majority of patients presented these skin lesions on the lower limbs. Two had idiopathic AB, 3 in association with venous insufficiency of the lower extremities and 6 with livedo reticularis (LR) and/or Raynaud's phenomenon (RP). Prior to our evaluation, most of these patients were diagnosed as having skin vasculitis and were treated with prednisone and/or cyclophosphamide. We conclude that AB is a distinct clinical entity with characteristic skin lesions affecting the legs. The disease is associated mainly with LR and RP. Very careful clinical assessment is needed to avoid incorrect diagnosis and unnecessary and potentially harmful therapeutic intervention.

摘要

在本报告中,我们描述了11例患有白色萎缩(AB)的希腊患者。所有患者均有特征性皮肤损害:瘀点或紫癜性丘疹或出血性大疱,这些损害会坏死并形成溃疡,进而发展为萎缩性瘢痕,周围皮肤伴有色素沉着。大多数患者的这些皮肤损害出现在下肢。2例为特发性AB,3例与下肢静脉功能不全相关,6例与网状青斑(LR)和/或雷诺现象(RP)相关。在我们进行评估之前,这些患者中的大多数被诊断为皮肤血管炎,并接受了泼尼松和/或环磷酰胺治疗。我们得出结论,AB是一种具有特征性皮肤损害、累及腿部的独特临床实体。该疾病主要与LR和RP相关。需要非常仔细的临床评估以避免误诊以及不必要的、可能有害的治疗干预。

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