Related Experiment Video
Updated: Mar 14, 2026

Refined Murine Model of Idiopathic Pulmonary Fibrosis
Published on: June 17, 2025
Novel Cutaneous Manifestations of Pleuroparenchymal Fibroelastosis
Christopher M Lowther1, Annie O Morrison, Nicole M Candelario
1*Big Horn Basin Skin Center, Cody, WY; †Department of Dermatology, Cockerell Dermatopathology, UT Southwestern, Dallas, TX; ‡Penrose-St Francis Hospital, Colorado Springs, CO; and §Department of Dermatology, Cockerell Dermatopathology, UT Southwestern, Dallas, TX.
Abstract:
Pleuroparenchymal fibroelastosis (PPFE) is a rare progressive disease that manifests as parenchymal fibrosis of the upper lobe and pleura. Approximately 100 cases have been reported. Cutaneous manifestations of PPFE have not previously been described. Diagnosis is dependent on histologic identification of fibrosis with atypical elastic fibers, necessitating an invasive peripheral lung wedge biopsy.A 68-year-old male with a history of pleuroparenchymal fibroelastosis presented with an asymptomatic, telangiectatic erythematous eruption on bilateral lower extremities. Biopsies demonstrated a subtle perivascular infiltrate with marked increase in atypical elastic fibers, similar to the elastosis in the patient's lungs.This is the first documented case of cutaneous manifestations in PPFE. Clinicians need to be aware that cutaneous eruptions clinically simulating telangiectasia macularis eruptiva perstans but lacking a mast cell infiltrate histologically, may have increased abnormal elastic fibers. Thus, early recognition of these lesions in patients with an undefined restrictive lung disorder, may facilitate the diagnosis of PPFE in some patients.
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