The Role of Free Perforator Flaps in Complex Post-Oncological Reconstruction: Insights into DIEP, ALT, and SCIP Flap Techniques
Background: Complex post-oncological reconstruction remains a cornerstone in restoring form and function following extensive oncological resections. Among the reconstructive options, free perforator flaps, including the deep inferior epigastric perforator (DIEP), anterolateral thigh (ALT), and superficial circumflex iliac perforator (SCIP) flaps, have emerged as versatile tools offering superior outcomes. Objective: This article evaluates the indications, surgical techniques, and outcomes associated with the use of DIEP, ALT, and SCIP flaps in managing complex defects in oncological reconstruction. Methods: A comprehensive review of the literature was conducted, focusing on patient selection, anatomical considerations, operative nuances, and postoperative results for each flap type. Results: DIEP, ALT, and SCIP flaps provide significant benefits, including reduced donor-site morbidity, reliable vascularity, and aesthetic outcomes. Each flap exhibits unique advantages depending on the reconstructive needs and patient characteristics, with tailored approaches enhancing both functional and cosmetic results. Conclusion: Free perforator flaps represent the gold standard for addressing complex reconstructive challenges in post-oncological surgery. An individualized, multidisciplinary approach is critical to optimize outcomes and patient satisfaction.
Authors
- Abigail Berenice Gómez Valenzuela
- Angélica Estefanía Carpinteiro Valero
- Joab Ulises Calderón Barrientos
Institutions
- Benemerito Hospital General con Especialidades "Juan Maria de Salvatierra" (MX)
- Institute for Social Security and Services for State Workers (MX)
Publication Details
- Journal
- International Journal of Medical Science and Clinical Research Studies
- Published
- 2025-02-19
- DOI
- https://doi.org/10.47191/ijmscrs/v5-i02-17
- Primary Topic
- Reconstructive Surgery and Microvascular Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00