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Review
. 2020 Dec 22;8(12):e3300.
doi: 10.1097/GOX.0000000000003300. eCollection 2020 Dec.

Treatment of Non-melanoma Skin Cancers in the Absence of Mohs Micrographic Surgery

Affiliations
Review

Treatment of Non-melanoma Skin Cancers in the Absence of Mohs Micrographic Surgery

Andrew M Ferry et al. Plast Reconstr Surg Glob Open. .

Abstract

Non-melanoma skin cancers are the most common malignancies globally. Although non-melanoma skin cancers exhibit low metastatic potential, they can be locally destructive, necessitating complex excisions and reconstructions. Mohs micrographic surgery is the gold-standard treatment for high-risk non-melanoma skin cancers in patients who are appropriate surgical candidates. Despite its efficacy, Mohs micrographic surgery is not readily available in most geographic regions, necessitating that plastic surgeons be well-versed in alternative treatment modalities for non-melanoma skin cancer. Herein, we will discuss the management of non-melanoma skin cancers in settings where Mohs micrographic surgery is not readily available.

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Conflict of interest statement

Disclosures: The authors have no financial interest to declare in relation to the content of this article. This study did not receive any support.

Figures

Fig. 1.
Fig. 1.
Incidence of non-melanoma skin cancers of the face.
Fig. 2.
Fig. 2.
Proper labeling of skin specimens. Skin specimens (including the outer layers of the skin) may be marked for orientation using a single suture at the 12 o’clock position (A). In contrast, deep specimens require a 3 o’clock or 9 o’clock suture so that the pathologist may identify the anterior aspect of the sample (B).
Fig. 3.
Fig. 3.
Patient with a post-excisional defect involving the entire vermillion of the lower lip (A). Application of biologic acellular dermal matrix (B). Patient 3 months postoperatively (C).
Fig. 4.
Fig. 4.
Patient with a large, circumferential defect of the infraorbital cheek following excision of her malignancy (A). The defect was reconstructed utilizing a cervicofacial flap (B). Patient 3 weeks postoperatively without signs of ectropion or lip retraction (C). Patient 1 year postoperatively with minimal scarring (D).
Fig. 5.
Fig. 5.
Patient with a full-thickness defect of the nasal ala following excision of a nonmelanoma skin cancer (A). Inset of the paramedian forehead flap into the alar defect (B). Patient 3 weeks post-operatively following inset of the flap (C). Patient 3 months postoperatively following flap division and inset (D).

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