06. Skin Malignancies

Resident Editor: John Landefeld, M.D.

Faculty Editor: Ryan Arakaki, M.D.

Background

  • Non-melanoma skin cancer (NMSC) is the most common cancer in humans
  • 75% of NMSCs are basal cell carcinomas; 25% of NMSC’s are squamous cell carcinomas
  • Melanoma incidence has risen from 1/100,000 to 15/100,000 over the last 40 years

Table 6: Skin Malignancies

Type

Description

Management

Actinic keratosis

- 1-2% progression per year to SCC if untreated

- Ill-defined, erythematous, scaly papule or plaque in sun-exposed areas

- Often better palpated than seen

- May itch or hurt

 

 

Individual lesions

- Cryotherapy

 

Field treatment for multiple lesions

- Imiquimod 5% cream BIW x16 weeks

- 5-FU 5% cream BID x2-4 weeks

- Photodynamic therapy (performed in the office, takes only one day, longer recovery time)

Squamous cell carcinoma

- Erythematous, scaly, indurated papule, plaque, or nodule.

- People describe nonhealing lesion that bleeds with minimal trauma

- Confirm diagnosis with biopsy before treatment

- In all-comers, 5% risk of metastases at the time of diagnosis

- In people with darker skin, 20-40% of metastases at the time of diagnosis

 

SCC In Situ:

- ED&C

- Simple excision

- Can consider imiquimod or 5-FU if the patient does not wish to have surgery

 

SCC:

- Simple excision

- Mohs micrographic surgery

 

 

Basal cell carcinoma

- Pearly papule or nodule with rolled borders and arborizing telangiectasias under dermoscopy

- Central, non-healing ulceration and/or pigment may be present

 

4 different pathologic subtypes:

- Nodular

- Infiltrative/Morpheaform

- Superficial

- Micronodular

 

Superficial BCC

- Electrodessication and curettage (ED&C)

- Imiquimod 5% cream M-F daily x6 weeks

- 5-fluorouracil 5% cream BID x3-12 weeks

 

Nodular, infiltrative, micronodular

- Options are ED&C (nodular only), simple excision, or Mohs micrographic surgery (especially for high risk)

- Choice of treatment will depend on size, depth, subtype, and anatomic site

- After treatment, will usually follow with derm q6-12 months for 2 years, then PCP

Melanoma

 

 

 

 

- Increasing incidence (2.2% lifetime risk), and accounts for 1% of cancer deaths

- Requisite full-body exam to check all of the patient’s lesions as well as to get a sense of their baseline nevi

- Look for “ugly duckling” that is different from the patient’s baseline nevi

- Can using “ABCDE” scoring to help decide on biopsy:

- Asymmetry

- Borders irregular

- Color (multi-colored)

- Diameter >6mm

- Evolution

- When in doubt, refer to derm

- Biopsy (performed by derm) should contain the entire lesion so that pathologist can accurately stage it (i.e. punch or excisional preferred, shave ok if lesion small and superficial)

- Excision and potential sentinel lymph node biopsy if tumor stage Ib or higher

- Refer to dermatologist or melanoma clinic for evaluation and management

Safe Sun Guidelines

  • Minimize sun exposure during the peak ultraviolet-B (UV-B) 10 a.m. to 4 p.m.
  • Apply sunscreen with UVA (not measured by SPF) and UVB protection (broad-spectrum means both UVA and UVB protection) of at least 30. Zinc or titanium-containing products are preferred. Also, remember UVA goes through windows (especially important for patients with photosensitive connective tissue diseases).
  • Persons should wear wide-brimmed hats, sunglasses, and protective clothing (e.g., tightly woven fabrics and long-sleeved shirts) when sun exposure cannot be avoided. Physical protection is stronger than sunscreen and preferable when an option.
  • Avoid deliberate sun tanning and use of tanning parlors. Tanning parlors are classified as Group 1 carcinogens by the WHO, a classification that includes cigarettes and plutonium.

References

Bolognia, J et al. Dermatology. 3rd Edition. 2011. Elsevier Ltd.