Literature DB >> 16476392

[Idiopathic atrophoderma of Pasini and Pierini. Study of 4 cases].

Alfonso González-Morán1, Rocío Martín-López, María L Ramos, Concepción Román, María P González-Asensio.   

Abstract

Idiopathic atrophoderma of Pasini and Pierini (IAPP) is an infrequent form of cutaneous atrophy, of unknown etiology. We describe the clinical and histological symptoms of four women with IAPP. Three of them had lesions on the back, while the fourth had them on the buttocks. The histological study of two patients revealed a variable degree of collagen alteration (sclerosis and hyalinization). In the other patients, the dermis was apparently normal. There is discussion about whether IAPP is a distinct entity or is related to morphea. Both sets of symptoms, although separate, could form part of the same spectrum within the fibrosing type of dermatoses. We found no positive serology for B. burgdorferi in our patients.

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Year:  2005        PMID: 16476392     DOI: 10.1016/s0001-7310(05)75059-6

Source DB:  PubMed          Journal:  Actas Dermosifiliogr        ISSN: 0001-7310


  2 in total

1.  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.  Idiopathic Atrophoderma of Pasini and Pierini: Case report and literature review.

Authors:  Anastasiya Muntyanu; Margaret Redpath; Osama Roshdy; Abdulhadi Jfri
Journal:  Clin Case Rep       Date:  2018-12-18
  2 in total

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