Simplifying Forehead and Temple Reconstruction: A Narrative Review.

J Clin Med

Department of Dermatology, University Clinic of Navarra, 28027 Madrid, Spain.

Published: August 2023

AI Article Synopsis

  • The forehead and temporal regions are common sites for skin cancer, requiring careful reconstruction after tumor removal to maintain facial symmetry and conceal scars.
  • Skin grafts and secondary wound healing often result in poor cosmetic outcomes, making skin flaps the preferred method for reconstruction when direct closure isn't possible.
  • Techniques like the frontalis myocutaneous transposition flap and the preauricular skin advancement flap are effective for closing larger defects on the forehead and temporal areas, respectively.

Article Abstract

The forehead and temporal region are frequent areas of skin cancer development. After tumor removal, reconstruction must be performed, maintaining the frontal-temporal line of the scalp and symmetry of the eyebrows in an attempt to hide the scars within these marks or natural folds and wrinkles. Second wound healing and skin grafts generally do not produce an acceptable cosmetic result. When direct closure is not possible, the technique of choice is skin flaps. In the midfrontal line continuation of the glabella, there is a remnant of skin to be used as a donor area for local flaps; similarly, it occurs in the preauricular cheek, which can move toward the temple. In addition to the classic advancement and rotation flaps, the frontalis myocutaneous transposition flap is an excellent technique for closing defects which are wider than higher on the forehead. Its design is very versatile and can be performed between the two pupil lines at different heights depending on the location of the defect. On the other hand, the preauricular skin advancement flap with an infralobular Burow's triangle is also an excellent option for reconstructing tumors in the temporal area.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455930PMC
http://dx.doi.org/10.3390/jcm12165399DOI Listing

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