none 10.31254/dentistry.2026.11102 BioMed Research Publishers BioMed Research Publishers 16195 194913437 314763 20260515013037558 10.31254 2026-05-15T01:30:47Z 2026-05-15T01:30:42Z 0 International Journal of Dentistry Research Int J Dentistry Res 25813218 10.31254/dentistry https://dentistryscience.com/ 4 29 2026 11 1 Filipa Reis Faculty of Dental Medicine, University of Lisbon, Lisbon, Portugal https://orcid.org/0009-0006-9609-6132 Isabel Gomes Oral and Biomedical Sciences Research Unit, Faculty of Dental Medicine, University of Lisbon, Lisbon, Portugal https://orcid.org/0000-0002-9509-7495 João Paulo Martins Oral and Biomedical Sciences Research Unit, Faculty of Dental Medicine, University of Lisbon, Lisbon, Portugal https://orcid.org/0000-0001-9330-772X Cátia Branco Faculty of Dental Medicine, University of Lisbon, Lisbon, Portugal https://orcid.org/0009-0009-3028-8934 Luís Miguel Lopes Laboratory for Instrumentation, Biomedical Engineering and Radiation Physics (LIBPhys), Lisbon, Portugal https://orcid.org/0000-0001-8633-827X Acrylic removable partial dentures have long been used to rehabilitate partially edentulous patients. Conventional fabrication workflows involve multiple clinical and laboratory procedures that require high precision, are time-consuming, and are susceptible to human error. The integration of computer-aided design and computer-aided manufacturing (CAD-CAM) technologies has enabled the development of streamlined digital workflows for prosthesis fabrication. This clinical report describes the rehabilitation of a partially edentulous patient using an acrylic removable partial denture produced through a fully digital workflow. An intraoral scan was obtained using an intraoral scanner, and the prosthesis was designed with CAD software. The denture was fabricated using stereolithography 3D printing in a monolithic tooth-colored resin, followed by characterization of the flanges with pink resin to simulate gingival tissues. The prosthesis demonstrated satisfactory functional and aesthetic outcomes during a 1-year follow-up period, and the patient reported a high level of satisfaction with the treatment. 4 29 2026 7 11 1 10.31254/biomed-crossmark-policy www.biomedresearch.org false 10.31254/dentistry.2026.11102 https://www.dentistryscience.com/IJDR_2026111_02.pdf