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Histological evaluation of palatal donor site healing with leukocyte–platelet–rich fibrin versus collagen sponge

  • José C. Rosas-Díaz
    ,
  • María E. Guerrero
    ,
  • Nancy E. Córdova-Limaylla
    ,
  • ,
  • Jerson J. Palomino-Zorrilla
    ,
  • Rocio del Carmen Alvarez-Medina
  • Universidad Privada San Juan Bautista
    ,
  • Universidad Nacional Mayor de San Marcos
    ,
  • ,
  • Universidad Científica del Sur
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

63488

Pages from-to (Number of pages)

Pages e79-e84

Journal (Volume, Issue Number)

Journal of Clinical and Experimental Dentistry (Volume 18, Issue 1)

Publication milestones

  • Published - 01/2026

Publication status

Published - 01/2026

Publication IDs

  • Scopus: 105028013595

Abstract

Background: The palate is the primary donor site for autogenous connective tissue grafts in periodontal and peri-implant plastic surgery, yet healing by secondary intention often results in morbidity. Collagen sponge (CS) and leukocyte–platelet-rich fibrin (L-PRF) have been proposed to enhance donor site repair, but comparative histological evidence in humans remains scarce. Objective: To compare the histological characteristics of palatal donor site healing following coverage with CS or L-PRF. Material and Methods: A retrospective cross-sectional histological study was performed on palatal biopsies collected four months after connective tissue graft harvesting covered with CS (n = 9) or L-PRF (n = 9). Epithelial type and thickness, lamina propria thickness, submucosal composition, inflammatory infiltrate, vascular congestion, and edema were evaluated using hematoxylin–eosin staining. Results: Both biomaterials supported uneventful healing without necrosis or severe inflammation. Compared with CS, L-PRF was associated with thicker epithelium, a higher frequency of hyperparakeratinization, and the presence of orthokeratinization. Lamina propria thickness was slightly greater in L-PRF, while fibrous submucosa predominated in both groups. Mild leukocyte infiltration and transient edema were more common with L-PRF, suggesting a more active regenerative response. Conclusions: CS and L-PRF both promoted favorable palatal donor site healing. L-PRF demonstrated histological features consistent with enhanced tissue regeneration, likely due to its growth factor content. These preliminary findings warrant validation in randomized controlled trials with larger sample sizes.