Literature DB >> 25054763

Case for diagnosis.

Carolina Mayana de Avila Batista1, Monica Oliveira Piantino Lemos1, Luis Eduardo de Almeida Prado Franceschi1, Carolina Borges Basilio1, Carmelia Matos Santiago Reis1.   

Abstract

Idiopathic Atrophoderma of Pasini and Pierini (IAPP) is a rare, exclusively cutaneous disease. It is more frequent in females, with incidence peak in the second and third decades of life. The etiopathogenesis remains unknown. IAPP most commonly affects the back, abdomen and proximal regions of the limbs. Lesions may be rounded, oval or circular; single or multiple. The evolution is variable and the course is initially progressive. Collagen changes such as atrophy, thinning, condensation and sclerosis may be observed in the papillary dermis. This paper describes a case of Idiopathic Atrophoderma of Pasini and Pierini with histopathologic findings.

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Year:  2014        PMID: 25054763      PMCID: PMC4148290          DOI: 10.1590/abd1806-4841.20142977

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN: 0365-0596            Impact factor:   1.896


  2 in total

Review 1.  Cutaneous Manifestations of Scleroderma and Scleroderma-Like Disorders: a Comprehensive Review.

Authors:  Caterina Ferreli; Giulia Gasparini; Aurora Parodi; Emanuele Cozzani; Franco Rongioletti; Laura Atzori
Journal:  Clin Rev Allergy Immunol       Date:  2017-12       Impact factor: 8.667

2.  Atrophoderma of Pasini and Pierini.

Authors:  Ricardo Ruiz-Villaverde; Daniel Sánchez-Cano; Luis Salvador-Rodriguez; Carlos Cuenca-Barrales
Journal:  Sultan Qaboos Univ Med J       Date:  2017-10-10
  2 in total

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