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Full-length video Where can I learn more about Mohs versus standard excision?
What is the key difference between Mohs and standard excision?

The Answer Is in the Margin

Both Mohs surgery and standard excision aim to remove skin cancer. The most important difference is not the shape of the incision. It is how the edge of the removed tissue—the surgical margin—is evaluated, and when that information becomes available.

Mohs surgery is built around complete mapped peripheral and deep margin assessment during the operation. Standard excision removes the visible tumor with a planned margin of normal-appearing skin; the specimen is then usually evaluated with representative vertical sections in a pathology laboratory.1–4

Think of the cancer as an irregular property and the margin as its fence line. Mohs creates a map of the fence and checks the mapped border. Standard excision removes a planned buffer around the property and checks scheduled cross-sections. Both approaches can work. The question is whether the cancer and the anatomy justify a continuous map or whether representative sections are sufficient.

That is the decision patients should remember:

“Do not ask which operation sounds more advanced. Ask whether having a mapped margin during surgery would change the safety, cure, tissue preservation, or reconstruction plan.”

- Dr. Hocker
Why can standard and wide local excision sound confusing?

Why Standard Excision and Wide Local Excision Can Sound Confusing

Patients often hear both terms. In basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC) guidance, standard excision usually means removal of the visible tumor with a planned clinical margin followed by routine pathology. Wide local excision, or WLE, is frequently used in studies and in everyday surgical language to describe the same general approach, although wide local excision has a more specific and familiar role in melanoma care.

The label is less important than four operational questions:

  1. How much tissue will be removed initially?
  2. How will the peripheral and deep margins be processed?
  3. When will the margin result be available?
  4. What happens if cancer remains at an edge?

Two surgeons can use the same procedure name and process the specimen differently. Conversely, different names can describe essentially the same margin strategy. Patients should ask about the method rather than relying on the label.

What does complete mapped margin assessment mean?

What Does Complete Mapped Margin Assessment Actually Mean?

The phrase does not mean that surgery can see the future or guarantee that a patient will never develop another cancer. It means the removed layer is oriented to the patient, mapped, and processed so its peripheral and deep surgical margin can be evaluated as an en face surface. If a positive focus is found, the surgeon can match it back to the wound.1–3

That distinction matters because three different ideas are often collapsed into the word margin:

  • Clinical margin: the normal-appearing rim planned around the visible tumor.
  • Specimen margin: the physical edge of the tissue that was removed.
  • Microscopic margin assessment: the method used to inspect that edge.

Mohs does not merely take a smaller clinical margin. Its defining advantage is that tissue removal and microscopic mapping form one feedback loop.

How does Mohs surgery work?

How Does Mohs Surgery Work?

In Mohs surgery, the surgeon removes the visible tumor with a narrow layer of surrounding tissue. The specimen is oriented, color-coded, divided when needed, and mapped to the wound. Frozen horizontal sections are prepared so the peripheral and deep margin can be evaluated as a mapped surface. If cancer remains, the map tells the surgeon where it remains. Another layer is removed only from that area. The cycle continues until the mapped margins are clear.1–3

The surgeon therefore performs three linked jobs:

  1. removes the cancer;
  2. interprets the margin tissue under the microscope; and
  3. returns to the exact positive location if another stage is needed.

This is why Mohs is described as both margin-controlled and tissue-sparing. It does not promise that every defect will be small. An extensive cancer still creates an extensive defect. The advantage is that subsequent tissue removal is directed to mapped positive areas.

How does standard excision work?

How Does Standard Excision Work?

In standard excision, the surgeon removes the visible tumor plus a predetermined clinical margin. The specimen is sent to a laboratory, where it is usually cut into vertical sections—often described as bread-loaf sections because the specimen is sliced like a loaf of bread.2,4

Each section provides an excellent cross-sectional view at that location. The tissue between the sections is not directly examined. That is not a flaw hidden from medicine; it is the known design of routine surgical pathology. It is appropriate when the tumor is well defined, low risk, and likely to be cleared by a standard planned margin.

A methodologic facial BCC study illustrates the difference without proving that standard excision usually fails. Researchers analyzed 42 small, well-defined, primary, nonmorpheaform facial BCCs excised with 2-mm margins and already known to have positive margins on Mohs processing. Simulated sections at 4-mm intervals detected residual BCC in 44% of the 50 positive margins. The lesson is not that routine excision misses half of all cancers. The lesson is that representative sections and a complete mapped margin answer different questions.5

A broader systematic review found that incomplete excision after standard excision remains a real clinical problem, but the studies varied greatly and did not directly compare standard excision with Mohs. Its useful lesson is to match the margin method to tumor risk rather than quote one universal miss rate.11

How do the margin-assessment methods compare?

Margin-Assessment Comparison

Margin-Assessment Comparison
FeatureMohs surgeryStandard excision
Tissue removalNarrow mapped layer, followed by additional tissue only where the map remains positiveVisible tumor plus a planned clinical margin removed at the first operation
Margin processingHorizontal/en face processing designed for complete mapped peripheral and deep margin assessmentRepresentative vertical sections through the specimen
Timing of resultDuring the surgical visitAfter laboratory processing; timing varies
If cancer remains at an edgeMore tissue is removed from the corresponding mapped locationRe-excision or another treatment may be needed after the pathology result
Strongest fitHigh-risk, recurrent, aggressive, poorly defined, or tissue-sensitive tumorsSelected well-defined, low-risk tumors where a planned margin is safe
Reconstruction sequenceRepair can often follow same-day mapped clearanceMajor repair may need to wait when meaningful margin uncertainty remains
When does Mohs add the most value?

When Does Mohs Add the Most Value?

Mohs is most useful when the margin information changes the decision. Common examples include:

A cancer that has already returned

A recurrent tumor has already shown that prior treatment did not achieve durable local control. Scar tissue can also blur borders and alter anatomy. Recurrent tumors are where a mapped search is especially valuable.

The strongest direct comparison comes from a randomized trial of facial BCC with 10-year follow-up. Among recurrent facial BCCs, recurrence was 3.9% after Mohs and 13.5% after standard excision.6 In plain English, that was about 1 recurrence in 25 after Mohs versus about 1 in 7 after standard excision: 9.6 fewer recurrences per 100 patients and about a 71% relative reduction in this specific high-risk population.

High-risk anatomy

The nose, eyelid, lip, ear, central face, hands, feet, and genital skin have little room for unnecessary tissue loss and little tolerance for persistent cancer. On the eyelid, a few millimeters can affect closure and eye protection. On the lip, they can affect oral competence. On the nose, they can change which flap or graft is possible.

High-stakes anatomy does not make Mohs automatically correct for every diagnosis. It makes the value of mapped margin assessment and tissue preservation much greater when the tumor is one that Mohs appropriately treats.1,2,7

Aggressive or poorly defined pathology

Infiltrative, morpheaform, micronodular, and related BCC patterns can extend beyond what is visible. cSCC with very-high-risk features can behave more aggressively and deserves a margin strategy matched to that risk. Current guidance favors Mohs or another form of peripheral and deep en face margin assessment (PDEMA) for many high-risk BCCs and very-high-risk cSCCs.1,2

Immune suppression

Solid-organ transplant recipients and other immunosuppressed patients can develop more numerous and more aggressive cSCCs. Mohs does not erase the biological risk of immune suppression, but complete mapped margin assessment may be particularly important when the tumor itself is high risk. These patients may also need closer surveillance and, in selected cases, imaging, nodal evaluation, radiation, or systemic therapy beyond surgery.2

Poorly defined clinical borders

Some cancers blend into sun-damaged skin, scar, inflammation, or prior treatment change. A wide visible margin can still miss an irregular extension; a very wide margin can also sacrifice healthy tissue unnecessarily. Mohs turns that uncertainty into a mapped microscopic search.

What does the recurrence evidence show?

What Does the Recurrence Evidence Show?

The evidence does not have one universal number because BCC and cSCC are different diseases, and primary low-risk tumors are not the same as recurrent or very-high-risk tumors.

Recurrent facial BCC: the clearest randomized comparison

Recurrent facial BCC: the clearest randomized comparison
Treatment10-year recurrence in recurrent facial BCC
Mohs surgery3.9%
Standard excision13.5%

These numbers come from one randomized trial and apply to recurrent facial BCC, not every skin cancer.6

Keratinocyte cancers across multiple studies

A 2024 systematic review and meta-analysis combined 17 studies and 6,503 keratinocyte cancers. Recurrence was 3.1% with micrographic surgery and 5.3% with conventional excision. The pooled relative risk was 0.48, which represents about a 52% relative reduction; the analysis reported an absolute reduction of 2.9 percentage points, or roughly one fewer recurrence for every 35 tumors treated with micrographic surgery.8

Evidence in numbersEvidence in Numbers: High-Risk Tumors Magnify the Margin Advantage

Evidence in Numbers: High-Risk Tumors Magnify the Margin Advantage

A separate meta-analysis of 28 high-risk keratinocyte-carcinoma studies found pooled recurrence of 3.9% after complete margin assessment versus 13.5% after sectional assessment. In the study subsets, recurrence was 9.8% versus 32.0% for cSCC with perineural invasion and 4.4% versus 11.9% for recurrent BCC.9

The complete-margin group included Mohs and related complete-margin techniques. The study therefore supports the margin-control principle rather than claiming that every tumor in the analysis underwent classic Mohs surgery.

Very-high-risk cSCC

There is no randomized Mohs-versus-standard-excision trial for cSCC. A recent 12-site observational study followed 2,752 very-high-risk cSCCs and associated complete margin assessment with lower adverse outcomes than standard vertical-section assessment.10

Evidence in numbersEvidence in Numbers: Very-High-Risk cSCC at Three Years

Evidence in Numbers: Very-High-Risk cSCC at Three Years

Evidence in Numbers: Very-High-Risk cSCC at Three Years
OutcomeMohs/PDEMAStandard excision with vertical sections
Local recurrence5.9%12.5%
Nodal metastasis6.0%11.6%
Distant metastasis1.9%4.3%
Disease-specific death3.3%6.2%

These are adjusted observational-cohort results, not a randomized trial. Their value is that the same direction of benefit appeared across local control, spread, and cancer-related death.10

These studies are observational, so they should not be presented as randomized proof. They do, however, reinforce the same clinical principle found in current guidelines: as cSCC risk rises, complete mapped margin assessment becomes more important.2

Why is there no single honest cure rate?

Why There Is No Single Honest Cure Rate

Websites often advertise one cure rate for Mohs as though every tumor were interchangeable. That is memorable but medically incomplete.

Recurrence depends on:

  • cancer type;
  • primary versus recurrent disease;
  • microscopic subtype;
  • location and size;
  • immune status;
  • prior radiation or treatment;
  • length and quality of follow-up;
  • whether the study counts local recurrence, nodal spread, or disease-specific death.

An older five-year estimate for primary low-risk BCC should not be pasted onto a recurrent infiltrative cSCC in an immunosuppressed patient. The strongest way to make the Mohs case is to use the correct number for the correct patient group. For recurrent facial BCC, that is the randomized 3.9% versus 13.5% 10-year comparison.6 For very-high-risk cSCC, the comparative evidence is newer and observational.10

The honest teaching point is still strongly pro-Mohs: when tumor risk and anatomy make residual cancer costly, complete mapped margin assessment is the most rational surgical design.

What are the tradeoffs of Mohs surgery?

What Are the Tradeoffs of Mohs?

Mohs is not a free advantage. Patients may spend several hours at the surgical visit because the tissue is processed one stage at a time. More than one stage may be required. The wound cannot be reconstructed until the margins are clear. The technique also depends on an appropriately trained surgeon, laboratory, and team.

Mohs can be unnecessary when a standard excision would predictably clear a low-risk tumor without sacrificing important tissue. Using a complex method where it adds no meaningful information wastes time and resources.

Standard excision has its own practical strengths:

  • it is familiar and widely available;
  • it provides conventional vertical sections showing tumor architecture and depth;
  • it can remove a low-risk tumor efficiently in one planned specimen;
  • it may be paired with immediate linear closure when the risk and margin plan support that sequence.

The comparison is not advanced versus primitive. It is mapped feedback versus planned removal with representative sectioning. The better method is the one whose information matches the clinical problem.

Why does tissue preservation matter?

Why Does Tissue Preservation Matter?

Tissue preservation is not cosmetic vanity. On the face and other constrained sites, normal tissue has jobs.

  • Eyelid skin closes and protects the eye.
  • Nasal tissue supports breathing and contour.
  • Lip tissue preserves speech, oral seal, and expression.
  • Ear tissue preserves shape and supports glasses or hearing devices.
  • Finger and genital skin preserve movement, sensation, and function.

A small randomized study of 30 nodular BCCs found a median defect area of 116.6 mm² after Mohs versus 187.7 mm² after standard excision, approximately 38% smaller.12 The study was small and does not prove universally better scars. It supports the mechanism: mapped removal can spare uninvolved tissue in selected tumors.

The most defensible claim is simple: Mohs is designed to remove additional tissue only where microscopic cancer remains. The final defect is still determined by the actual cancer.

Why should the margin plan come before the repair?

Why Should the Margin Plan Come Before the Repair?

Skin cancer removal and reconstruction are connected, but they are different decisions.

  1. Cancer decision: Is the tumor clear, and how was that determined?
  2. Reconstruction decision: What repair best fits the actual defect after clearance?

A flap moves nearby tissue into the wound. A graft brings skin from another site. Both can produce excellent results. But moving tissue changes landmarks. If a significant margin question remains, a later re-excision can become more complicated.

Current BCC and cSCC guidance therefore supports a margin-first sequence when complex tissue rearrangement would otherwise precede clear-margin confirmation.1,2 This is conditional, not a blanket prohibition against flaps after standard excision. A low-risk tumor removed with an appropriate plan may be safely repaired at the same operation. The principle is that the certainty required before repair should match the tumor risk and reconstruction complexity.

Mohs often resolves both steps in one visit: mapped clearance first, reconstruction after the actual defect is known. The Mohs surgeon may perform the repair, or reconstruction may be coordinated with plastic surgery, oculoplastic surgery, facial plastic surgery, otolaryngology, or another specialist when the anatomy requires it.

When is standard excision a good choice?

When Is Standard Excision a Good Choice?

Standard excision is not an inferior operation used when Mohs is unavailable. It is the right operation for many appropriately selected tumors.

It commonly fits when the tumor is:

  • primary rather than recurrent;
  • small and well defined;
  • low risk under current diagnosis-specific guidance;
  • located on the trunk or an extremity where a standard margin is safe;
  • not showing aggressive pathology or clinically important nerve involvement;
  • in a patient whose overall plan does not require same-day mapped information.1,2,13

The key is honest risk classification. A low-risk tumor should not be upgraded merely because Mohs is technically possible. A high-risk facial tumor should not be treated like a low-risk trunk lesion merely because both are called BCC.

When might surgery not be necessary?

When Might Surgery Not Be Necessary?

Some patients do not need Mohs or standard excision. Depending on the diagnosis and risk, a cancer-specific option such as electrodesiccation and curettage (ED&C), topical therapy, or radiation may fit; carefully selected patients with low-risk BCC and major competing health risks may reasonably choose observation.1,2

These paths are not interchangeable. A topical medication that fits a superficial BCC does not become a substitute for Mohs in an infiltrative recurrent nasal BCC. Use the diagnosis-specific treatment guide to compare the appropriate options.

Which treatment path usually fits the situation?

Decision Table: Which Path Usually Fits?

Decision Table: Which Path Usually Fits?
Clinical situationPath usually consideredWhy
Recurrent facial BCCMohs strongly favoredBest direct randomized evidence and mapped search through scarred anatomy
Primary BCC on the nose, eyelid, lip, or central faceMohs often favoredHigh-stakes anatomy and tissue preservation; confirm tumor-specific risk
Infiltrative or morpheaform BCCMohs/PDEMA often favoredSubclinical extension can exceed the visible edge
Very-high-risk cSCCMohs/PDEMA preferred in many surgical candidatesCurrent guidance and comparative cohorts favor complete margin control
Small, well-defined, low-risk BCC on the trunkStandard excision often appropriateA planned margin is usually safe; Mohs may add little
Small, low-risk cSCC on a low-risk extremity siteStandard excision often appropriateRisk and anatomy may not require mapped surgery
Superficial low-risk lesion in a suitable patientNonsurgical or simpler treatment may fitCancer-specific topical therapy, ED&C, or observation may be reasonable
Melanoma or rare tumorDiagnosis-specific specialist planThe correct pathway may involve WLE, staged excision, Mohs, immunostains, staging, or multidisciplinary care
What do common decision changes look like?

Four Examples That Show How the Decision Changes

Example 1: A small nodular BCC on the back

The tumor is primary, well defined, in a low-risk location, and has no aggressive subtype. Standard excision may clear it efficiently with an appropriate planned margin. ED&C may also be reasonable in a suitable lesion. Mohs would be technically possible but may add little.

Example 2: A recurrent infiltrative BCC on the nose

Recurrence, aggressive histology, high-stakes anatomy, and limited spare tissue all point in the same direction. Mohs is strongly favored because the margin is hard to predict and the reconstruction should be based on the true defect.

Example 3: A small cSCC on an extremity in an immunocompetent patient

If the tumor is primary, well differentiated, shallow, well defined, and otherwise low risk, standard excision may be appropriate. The same diameter would not guarantee the same answer on the ear or in a transplant recipient.

Example 4: A very-high-risk cSCC with nerve involvement

Mapped margin assessment is only one part of the plan. Mohs/PDEMA may be preferred for local control, but imaging, nodal evaluation, radiation, or systemic therapy may also require discussion. Mohs is a treatment for the primary tumor margin; it does not replace staging.2

What should I ask my dermatologist or surgeon?

Questions to Ask Your Dermatologist or Surgeon

  • Is my tumor low risk, high risk, or very high risk—and which exact features create that category?
  • Are the clinical borders well defined?
  • How will the peripheral and deep margins be evaluated?
  • Will I know the margin result before a flap or graft is performed?
  • What is the chance that a second operation will be needed if standard excision is used?
  • Does Mohs offer a meaningful tissue-preservation advantage at this site?
  • Is a nonsurgical option medically appropriate for this exact tumor?
  • Does the diagnosis require staging or treatment beyond margin clearance?
Frequently asked questions about Mohs versus excision

Frequently Asked Questions

Is Mohs always better than standard excision?

No. Mohs adds the most value when complete mapped margin assessment, tissue preservation, recurrence risk, or reconstruction planning matters. Standard excision is often the right choice for a well-defined, low-risk tumor where a planned margin is safe.

Does Mohs examine the entire margin?

Mohs is designed to examine the complete mapped peripheral and deep surgical margin with horizontal/en face processing. The technically useful phrase is complete mapped margin assessment; it is more precise than treating 100% as a magic guarantee.1–3

Does standard pathology examine only 1% of the margin?

Published estimates vary because specimens, section intervals, and processing methods differ. The durable teaching point is that routine vertical sections are representative samples with intervals between them, whereas Mohs creates a mapped en face assessment.3–5

Can Mohs and plastic surgery be used together?

Yes. The cancer can be cleared with Mohs and the defect repaired by the Mohs surgeon or another reconstructive specialist. The important sequence is margin strategy first, reconstruction second.

Can reconstruction happen the same day as Mohs?

Often, yes. Once the mapped margins are clear, the repair can commonly be planned around the actual defect. Some complex cases are deliberately staged or coordinated with another specialist.

Does a high cure rate mean I do not need follow-up?

No. A person who has developed one skin cancer has an increased risk of another. High-risk cSCC and immunosuppressed patients may also need more intensive surveillance. Follow the schedule recommended by the treating dermatologist.

Is Mohs used for melanoma?

Melanoma follows a diagnosis-specific pathway. Do not apply BCC/cSCC margin rules; use the melanoma treatment guide.

What if my prior excision has positive margins?

Positive margins mean tumor reaches an examined edge. The next step depends on cancer type, location, risk, prior repair, and whether mapped surgery would improve clearance. Recurrent or incompletely treated facial BCC or cSCC deserves a serious Mohs discussion.

Where should I go next in the Patient Journey?

Next Steps in the Patient Journey

  • First decide whether the tumor is low risk or high risk.
  • Review Do I Need Mohs Surgery? for a diagnosis-specific appropriateness framework.
  • If Mohs is planned, continue to What Happens on the Day of Mohs Surgery?
  • Compare the treatment menu for BCC, cSCC, melanoma, or the diagnosed rare tumor.
  • Share this guide with the treating dermatologist or surgeon and ask how the margins will be evaluated.
  • Consider consultation with a fellowship-trained Mohs surgeon when mapped margin control may change the plan.
Who reviewed and authored this comparison guide?
Portrait of Dr. Thomas L.H. Hocker

About the Author

Dr. Thomas L.H. Hocker is a Harvard- and Mayo Clinic-trained, triple board-certified dermatologist, Mohs surgeon, and dermatopathologist. He is the Founding Director of Dermatologic Surgery at the UMKC School of Medicine and University Health and an Iron Surgeon lecturer at the American Society for Dermatologic Surgery. His work focuses on Mohs surgery for melanoma, complex and rare skin tumors, and aesthetic reconstruction after skin-cancer treatment. He co-authored the best-selling textbook Review of Dermatology and created Skin Trust to give patients and clinicians free access to clear, current, evidence-based education.

Read Dr. Hocker's background and mission

Dr. Hocker earned his bachelor's degree with honors from Yale University, where he was inducted into Phi Beta Kappa. As a Winston Churchill Scholar, he then studied at the University of Cambridge and earned an M.Phil. in Organic Chemistry. He received his M.D. with honors from Harvard Medical School, where his research focused on melanoma genetics. He completed dermatology residency at Mayo Clinic, a dermatopathology fellowship at the University of Michigan, and a Mohs micrographic and reconstructive surgery fellowship at Mayo Clinic. He is board-certified in Dermatology, Dermatopathology, and Mohs Micrographic Surgery.

Dr. Hocker serves as the Founding Director of Dermatologic Surgery at the UMKC School of Medicine and University Health. He is an internationally invited lecturer and speaker who teaches about Mohs surgery for melanoma, complex and rare tumors, dermatopathology, and aesthetic reconstruction after skin-cancer treatment. He has also been selected as an Iron Surgeon lecturer by the American Society for Dermatologic Surgery. He is the co-author of Review of Dermatology, a best-selling dermatology review textbook, and he continues to teach and mentor medical students, residents, and physicians.

Skin Trust exists because Dr. Hocker believes access to excellent medical knowledge should not depend on geography, wealth, or proximity to a major academic center. After training at several of the world's leading institutions, he sees that education as both a gift and a responsibility: to translate current evidence, expert judgment, and hard-won clinical experience into guidance that patients, families, and clinicians can actually use.

The mission is to increase awareness, reduce avoidable suffering, and give every person equal access to trustworthy, up-to-date information that can help them make the best decisions for their life. Skin Trust also extends Dr. Hocker's lifelong commitment to teaching, writing, and mentoring medical students and residents as they build lives and careers of purpose and service.

For Dr. Hocker, this work is also an expression of faith. He regards the opportunities to learn at Yale, Cambridge, Harvard, Mayo Clinic, and the University of Michigan as blessings from God. Teaching, writing, mentoring, and building Skin Trust are ways to pay those blessings forward in service to patients, learners, and the broader community. His faith is the personal motivation to do this work carefully, generously, and with integrity; it is not a condition of using or benefiting from this free resource.

References for this Mohs-versus-excision guide

References

  1. National Comprehensive Cancer Network. Basal Cell Skin Cancer. Version 2.2026.
  2. National Comprehensive Cancer Network. Squamous Cell Skin Cancer. Version 2.2026.
  3. Tolkachjov SN, Brodland DG, Coldiron BM, et al. Understanding Mohs micrographic surgery: a review and practical guide for the nondermatologist. Mayo Clin Proc. 2017;92(8):1261-1271. DOI: 10.1016/j.mayocp.2017.04.009. PMID: 28778259.
  4. Wehner MR. Keratinocyte carcinoma: a review. JAMA. 2026;335(1):70-81. Published online October 30, 2025. DOI: 10.1001/jama.2025.18749. PMID: 41165676.
  5. Kimyai-Asadi A, Goldberg LH, Jih MH. Accuracy of serial transverse cross-sections in detecting residual basal cell carcinoma at the surgical margins. J Am Acad Dermatol. 2005;53(3):469-474. DOI: 10.1016/j.jaad.2005.02.049. PMID: 16112355.
  6. van Loo E, Mosterd K, Krekels GAM, et al. Surgical excision versus Mohs micrographic surgery for basal-cell carcinoma of the face: a randomized trial with 10-year follow-up. Eur J Cancer. 2014;50(17):3011-3020. DOI: 10.1016/j.ejca.2014.08.018. PMID: 25262378.
  7. Connolly SM, Baker DR, Coldiron BM, et al. AAD/ACMS/ASDSA/ASMS 2012 appropriate-use criteria for Mohs micrographic surgery. J Am Acad Dermatol. 2012;67(4):531-550. DOI: 10.1016/j.jaad.2012.06.009. PMID: 22959232.
  8. Lacerda PN, Lange EP, Luna NM, Miot HA, Abbade LPF. Efficacy of micrographic surgery versus conventional excision in reducing recurrence for basal cell carcinoma and squamous cell carcinoma: a systematic review and meta-analysis. J Eur Acad Dermatol Venereol. 2024;38(6):1058-1069. DOI: 10.1111/jdv.19743. PMID: 38116955.
  9. Fraga SD, Besaw RJ, Murad F, Schmults CD, Waldman A. Complete margin assessment versus sectional assessment in surgically excised high-risk keratinocyte carcinomas: a systematic review and meta-analysis. Dermatol Surg. 2022;48(7):704-710. DOI: 10.1097/DSS.0000000000003462. PMID: 35778249.
  10. Wang DM, Ran NA, Granger EE, et al. Excision with total margin control versus vertical section margin assessment for NCCN very-high-risk cutaneous squamous cell carcinoma. J Natl Compr Canc Netw. 2025;23(12):531-537. DOI: 10.6004/jnccn.2025.7072. PMID: 41671454.
  11. Nolan GS, Kiely AL, Totty JP, et al. Incomplete surgical excision of keratinocyte skin cancers: a systematic review and meta-analysis. Br J Dermatol. 2021;184(6):1033-1044. DOI: 10.1111/bjd.19660. PMID: 33131067.
  12. Müller FM, Dawe RS, Moseley H, Fleming CJ. Randomized comparison of Mohs micrographic surgery and surgical excision for small nodular basal cell carcinoma: tissue-sparing outcome. Dermatol Surg. 2009;35(9):1349-1354. DOI: 10.1111/j.1524-4725.2009.01240.x. PMID: 19500127.
  13. Kim JYS, Kozlow JH, Mittal B, et al. Guidelines of care for the management of cutaneous squamous cell carcinoma. J Am Acad Dermatol. 2018;78(3):560-578. DOI: 10.1016/j.jaad.2017.10.007. PMID: 29331386.