116 results match your criteria: "Atrophoderma of Pasini and Pierini"

BULGARIAN PATIENT WITH ATROPHODERMA OF PASINI AND PIERINI- DESCRIPTION OF A CASE AND SHORT UPDATE.

Georgian Med News

November 2023

1Onkoderma - Clinic for Dermatology, Venereology and Dermatologic Surgery, Sofia, Bulgaria; 4Department of Dermatology and Venereology, Medical Institute of Ministry of Interior, Sofia, Bulgaria.

Article Synopsis
  • Atrophoderma of Pasini and Pierini is a rare, benign skin condition characterized by single or multiple asymptomatic atrophic plaques, predominantly affecting women of European descent, usually appearing in their 20s or 30s.
  • Recent reports suggest a potential link between this condition and COVID-19, with a notable case of rapid progression post-infection observed in a 63-year-old female patient who was initially misdiagnosed with morphea.
  • Accurate diagnosis relies on histopathological verification and clinical examination, as the condition often resembles morphea and may lead to treatment delays if not correctly identified.
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Article Synopsis
  • Atrophoderma of Pasini and Pierini (APP) is a rare skin condition mainly found in young women, marked by hyperpigmented, depressed patches without surrounding redness.
  • A case study highlights a 43-year-old South Asian male with a history of multiple asymptomatic, bluish-brown plaques on his body, leading to a diagnosis of idiopathic atrophoderma of Pasini and Pierini (IAPP).
  • The report also includes a review of existing literature on IAPP to provide further insights into the condition.
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Combined high-frequency and Doppler ultrasound in early diagnosis of atrophoderma of Pasini and Pierini.

An Bras Dermatol

October 2019

Discipline of Dermatology, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Article Synopsis
  • Atrophoderma of Pasini and Pierini is a skin condition that results in depressed, well-defined plaques due to changes in dermal collagen.
  • Diagnosis often involves comparing affected skin to healthy skin from the same area, as the histopathological changes are not very distinct.
  • High-frequency ultrasound can effectively diagnose atrophic skin changes, and a case study demonstrates its utility in supporting both clinical and histopathological diagnoses.
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Atrophoderma of Pasini and Pierini in a young adult: a case report.

Acta Dermatovenerol Alp Pannonica Adriat

March 2019

Nuclear Medicine Department, University Clinical Center, Prishtina, Kosovo.

Article Synopsis
  • Atrophoderma of Pasini and Pierini is a skin condition characterized by sharply defined, darkened patches that appear slightly depressed, which can merge into larger areas of atrophy.
  • First identified in 1923 and 1936, this condition differs from other skin diseases due to its unique morphology and clinical presentation.
  • Although initially linked to Borrelia burgdorferi infection, current theories suggest that genetic, neurogenetic, and immunological factors may contribute to its development, as illustrated by a patient with widespread atrophic skin lesions and no known tick bite history.
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Article Synopsis
  • - Idiopathic Atrophoderma of Pasini and Pierini is a skin condition that should be considered when a patient has an asymptomatic atrophic skin plaque.
  • - It can be difficult to distinguish this condition from Linear Atrophoderma of Moulin and morphea.
  • - Diagnosis can be aided by observing specific features and performing a tissue biopsy.
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Article Synopsis
  • A 45-year-old Chinese man developed facial asymmetry 30 years ago, along with vision issues in his right eye and weakness on the left side of his body.
  • Over time, he experienced the emergence of brownish, atrophic patches on his side, which he reported had not been associated with trauma or other skin conditions.
  • After a long period without progression of the lesions, he sought medical advice in November 2010 for a diagnosis and prognosis of his condition, confirming he had no history of tick bites or seizures.
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Idiopathic atrophoderma of Pasini and Pierini: A case study of collagen and elastin texture by multiphoton microscopy.

J Am Acad Dermatol

November 2017

Biophotonics Group, Department of Quantum Electronics, Institute of Physics Gleb Wataghin, University of Campinas, Campinas, Brazil; National Institute of Science and Technology on Photonics Applied to Cell Biology, University of Campinas, Campinas, Brazil; Department of Physics, Federal University of Ceara, Fortaleza, Brazil.

Background: The diagnosis of idiopathic atrophoderma of Pasini and Pierini (IAPP) relies on typical clinical features, particularly distinctive pigmented ovular/round depressed plaques. Histologic examination often reveals no obvious changes, but patterns of collagen distribution, using multiphoton imaging and second harmonic generation can help track hidden details of tissue organization contributing to atrophy.

Objective: To identify histologic features that distinguish IAPP from unaffected skin.

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Linear atrophoderma of Moulin: an underrecognized entity.

Pediatr Rheumatol Online J

October 2015

Division of Dermatology, Department of Pediatrics, Montreal Children's Hospital, McGill University Health Centre, 1001 Boulevard Décarie, Montreal, QC, H4A 3J1, Canada.

Linear atrophoderma of Moulin (LAM) is an acquired skin condition that manifests in early childhood and adolescence. It likely represents a form of cutaneous mosaicism that presents with linear, hyperpigmented and atrophic lesions appearing on the trunk and limbs. Its clinical appearance varies and may closely resemble that of atrophoderma of Pasini and Pierini (APP) and linear scleroderma.

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