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Idiopathic atrophoderma of Pasini and Pierini: A case report and review of the literature

机译:Pasini和Pierier的特发性萎缩症:一例病例报告并文献复习

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Idiopathic atrophoderma of Pasini and Pierini (IAPP) is a type of rarely seen dermal atrophy which little sunken from the skin, characterized with sharp edged plaque le-sion. Lesions frequently placed symmetrically and not cause to subjective complaint. It is not certain whether IAPP is a different entity or it is a primary atrophic variant of morphea. Seventeen year-old male patient applied to our clinic with complainant of many slightly sunken from skin brown color spots that settle the front of body and at the middle line of back. The patient was diagnosed of IAPP according to clinical and histopathological findings. In this case of presentation, the clinical and histopatho-logical features of the IAPP has been described and other atrophic dermatosis and their distinctive features have been excluded in the discussion
机译:帕西尼和皮埃里尼(IAPP)的特发性萎缩症(IAPP)是一种罕见的皮肤萎缩症,很少从皮肤下陷,其特征是边缘锐利的斑块病变。病变通常对称放置,不会引起主观不适。不确定IAPP是不同的实体还是它是吗啡的主要萎缩变体。一名17岁的男性患者在我们的诊所接受了治疗,主诉许多浅褐色的皮肤褐色斑点沉入了身体的前部和背部的中线。根据临床和组织病理学发现,该患者被诊断为IAPP。在这种情况下,已经描述了IAPP的临床和组织病理学特征,并且在讨论中排除了其他萎缩性皮肤病及其独特特征。

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