See spot change: Lesion identification and management in primary care ERIN HENNESSEY DNP, APRN, FNP-C

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See spot change: Lesion identification and management in primary care ERIN HENNESSEY DNP, APRN, FNP-C Learning objectives Discuss malignant and benign skin lesions commonly seen in primary care. Identify common treatments and surgical procedures utilized for management. Review criteria for referral to appropriate specialty. Commonly seen malignant skin lesions in primary care. 1) Basal cell carcinoma 2) Squamous cell carcinoma 3) Melanoma 1

Commonly seen non malignant lesions Acrochordon (skin tag) Keloid Hypertrophic Scars Epidermal inclusion cyst Lipoma Seborrheic Keratosis Skin Cancer Screening Recommendations from Various Organizations ORGANIZATION American Academy of Dermatology; Skin Cancer Foundation; and American Cancer Society RECOMMENDATION Annual complete skin examination for all patients Annual complete skin examination for all patients Age 20 to 39 years: complete skin examination every three years Age 40 years and older: annual complete skin examination U.S. Preventive Services Task Force and American Academy of There is insufficient evidence to recommend for or against Family Physicians Policy Recommendation for Periodic Health routine complete skin examination. Examination* Physicians should be alert to potentially malignant lesions when examining patients for other reasons, especially when they have risk factors for melanoma, and should consider referring patients with marker lesions (i.e., atypical nevi) to a skin cancer specialist. Non Melanoma and Melanoma Skin Cancer History and Physical With evaluating lesions that may be non healing or present for an extended period of time, it is helpful to obtain the following: - Ethnicity and skin color (fair, olive, African American) - Lifetime sun exposure (frequent vs. intermittent) - History of sunburn as a child or adult - Tanning bed use - Smoking or chewing tobacco use - Occupational exposure - Immunosuppression or organ transplantation (renal transplant patients have a 253 fold increase in the risk for squamous cell carcinoma) - History of radiation treatment for cancer or previous PUVA or UVA treatment for psoriasis 2

Basal Cell Carcinoma Basal cell carcinoma is the most common invasive malignant cutaneous neoplasm. It is traditionally diagnosed by clinical identification and shave or scoop biopsy. The most common presenting complaint is a bleeding or scabbing sore that heals and recurs. Although it will not metastasize, if left untreated it will advance by direct extension and destroy normal tissue causing significant damage. Basal Cell carcinoma Basal cell carcinoma Inferior lateral canthus Nodular Basal Call Carcinoma Left cheek / side burn area BCC Note the rolled borders BCC 3

- these folks took tanning to a whole new level Actinic Keratosis Management single lesions of Actinic Keratosis Cryotherapy CO2 laser resurfacing, dermabrasion and chemical peels. Electrodessication and Curettage Surgical excision 4

Management of multiple or diffuse actinic keratoses Field Directed therapy total sun avoidance is recommended. 5-fluorouracil topically applied chemotherapy agent Imiquimod- topically applied chemotherapy agent Picato (ingenol mebutate) plant based (Euphorbia puplus) from Australia Management of multiple or diffuse actinic keratoses (con t) PDT photo dynamic therapy topical chemotherapy provides much better histologic response Diclofenac (Solaraze) BID for 60 90 days great placebo control studies in transplant patients out of Germany: a complete clearance of AK lesions was achieved in 41% (9/22) compared to 0% (0/6) in the vehicle group. At 24 months 55% of the patients had recurrent AKs but there were 0 SCC within the group. Squamous Cell carcinoma invasive Squamous cell carcinoma Squamous cell carcinoma In situ Squamous cell carcinoma Of the lower right lip 5

Management of Basal cell and Squamous Cell carcinoma Mohs procedure PDT Electrodesiccation and curettage Surgical Excision Erivedge (vismodegib) Malignant Melanoma Malignant melanoma is a cancerous neoplasm of pigment forming cells, melanocytes, and nevus cells. Clinically it s hallmarks are: irregularly shaped and pigmented patches, papules or plaques. Melanoma can arise from a preexisting lesion or de novo. There is no difference in the survival rate, but melanoma arising from a pre-existing lesion is more commonly found on the trunk, in younger individuals, and is more likely to be superficial spreading The earlier melanoma is diagnosed the better the changes of complete surgical eradication. Down and dirty - New research shows that having more than 11 nevi on one arm can indicate a increased risk for melanoma and patients can be appropriately advised to follow up with yearly skin exams Melanoma Cutaneous melanoma types: Superficial spreading melanoma Nodular melanoma Acral lentiginous melanoma Lentigo maligna melanoma 6

Epidemiology and Pathogenesis Melanoma is the fifth most common cancer in men and the sixth most common cancer in women. 1 in 50 Americans will develop melanoma in their lifetime For historical perspective, in 1935, the risk was 1 in 1500. The majority of melanoma in the US is diagnosed in the 15 50 year old age group. Patient with acute, episodic exposures to sunlight have a greater chance of developing melanoma than those with continuous exposure in either adulthood, adolescence or via occupational exposure. ABCDEs of identifying characteristics. A asymmetry B Border irregularity C Color variegation D Diameter > 6mm or approximately the size of a pencil eraser E Evolution or change Lesions can be red, white, blue, have notched borders or a papule or nodule within it. Ugly duckling rule 10% of melanoma do not follow the traditional rules. When a patient presents with any pigmented lesion that appear different from other nevi, it should be biopsied. Malignant Melanoma 7

Melanoma of the Lip Superficial spreading melanoma 70% of ALL cutaneous melanoma Location: Most commonly found on the trunks of men and the extremities of women (questionable correlation with intermittent sun exposure) Asymmetrical presentation with variation in color and border irregularities are common Papular or nodular component to the lesion may suggest a deeper invasion Can arise from preexisting moles Nodular melanoma Nodular melanoma comprises 9-20% or invasive melanoma Occurs most often in the fifth or sixth decade and more often in men than women 2:1 It does not conform to the usual pattern is it occasionally flesh colored and resembles a flesh colored nevi or basal cell carcinoma. It is most frequently misdiagnosed as a blood blister, hemangioma, nevus, seborrheic keratosis or dermatofibroma. They have rapid growth patterns and tend to ulcerate. 8

Lentigo Maligna Melanoma 4 15% of melanomas Located on the head, neck, arms and sun damaged skin Slow growing: 5 20 years Most commonly presents in the sixth or seventh decade Clinically appears as a brown to black or blue to black nodule Acral lentiginous melanoma 2 7% found in Caucasians 30 75% of melanomas in African American, Asian and Hispanic Located on the palms or soles as well as within the proximal nail fold Management of melanoma A punch biopsy is performed and lesions are micro staged by a pathologist. If there is extension to the border, a wider excision is indicated. Breslow thickness, ulceration status, mitotic rate, peripheral and deep margin status, anatomic level of invasion and tumor infiltrating lymphocytes are all factored into the staging process. Surgical margins for invasive melanoma should be at least 1 2 cm clinically measured around the primary tumor. The decision to perform sentinel node biopsy is based on clinical staging. Pathologic stage 0 IA do not routinely need node biopsy. 9

Acrochordon (skin tag) Frequently found in areas of rubbing Characterized by multiple round, black, or oval exophytic lesions attached by short broad to narrow stalks. The most frequent area we see these in are the axilla (48%) Correlation with patients that have T2DM, obesity, hyperlipidemia, and adenomatous polyps. No causation noted in studies. Pigmented skin tags and non pigmented 10

Dermatosis Papulosa Nigra Keloid vs Hypertrophic scar Caused by injury or surgery Hypertrophic Scar inappropriately large but remains confined to the wound site and in time regresses. Keloid Scar extends beyond the margins of injury and are often symptomatic (tenderness, pain, hyperesthesia). Histologically keloid scars have large collagen bundles and hypertrophic scars do not. Keloid Scar 11

Epidermal Inclusion Cyst The common epidermal or sebaceous cyst occurs primarily of the face, back, base of the ears, chest, and back, but can occur on any skin surface. The cyst wall is lined with stratified squamous epithelium which produces keratin. They may vary in size from a few millimeters to several centimeters. Treatment fluctuant and inflamed cysts must be excised and evacuated. If the cyst wall or sack is not excised, there is a possibility that the cyst can recur. Antibiotics are not usually necessary for non inflamed draining cysts. Epidermoid cyst Lipoma Lipomas are freely mobile, non pulsatile, exophytic skin masses. Usually are non tender, doughy feeling They are non malignant, but can be excised if they are enlarging, causing pressure on a nerve or blood vessel. Also called fatty tumors by some. They can be quite large. 12

An advanced basal cell carcinoma on the nare / nasal ala Significant retraction and destruction of the surrounding tissue. 13

In the pipeline Sunscreen Scientists out of Yale have developed a method for encapsulating padimate O creating a bio adhesive nano particle that adheres to the stratum corneum and does not absorb into the skin. It is water resistant, but comes off with towel friction. Field treatment for actinic keratosis - Low-dose 5-FU/SA is an effective and well-tolerated treatment option licensed for the lesion-directed treatment of mild-to-moderate hyperkeratotic AK lesions and currently under investigation for field-directed treatment. Europe has developed guidelines for the treatment of actinic keratosis recently and I expect the US to adopt similar guidelines in the next couple years. Clinical snapshot If you suspect a non melanoma skin cancer on evaluation, shave or scoop biopsy is appropriate. For a suspected melanoma or pigmented nevus biopsy, punch is recommended to obtain Breslow thickness which better predicts prognosis. Encourage all patients to utilize chemical free sunscreen. Benefits of wearing chemical containing sunscreen outweigh the risk of damage from UVA and UVB rays in the absence of a better option. SPF 30 50 is recommended. Any SPF below 12 will prevent burn, but provide no protection against UVA / UVB radiation. Follow up for patients who have AKs or have had BCC or SCC treated should be evaluated once yearly with a full body skin exam. Patient s with a history of melanoma should be evaluated with a full body skin exam every 3 months for the first year then every 6 months or yearly there after. Patient s who have greater than 11 nevi on one arm on physical exam should be advised to obtain once yearly skin checks. References Bradford PT, Goldstein AM, McMaster ML, Tucker MA. Acral lentiginous melanoma: incidence and survival patterns in the United States, 1986-2005. Arch Dermatol. 2009 Apr;145(4):427-434. doi: 10.1001/archdermatol.2008.609. Claas Ulrich, Antje Johannsen, Joachim Röwert-Huber, Martina Ulrich, Wolfram Sterry, Eggert Stockfleth Skin Cancer Centre Charité, Department of Dermatology, Charité Universitätsmedizin, Charité-Platz 1, 10117 Berlin, Germany Deng, Y., Ediriwickrema, A., Yang, F., Lewis, J., Girardi, M., & Saltzman, W. M. (2015). A Sunblock Based On Bioadhesive Nanoparticles. Nature Materials,14(12), 1278 1285. http://doi.org/10.1038/nmat4422 Habif, T. P. (2004). Clinical dermatology: A color guide to diagnosis and therapy. Edinburgh: Mosby. Lin, W. M., Luo, S., Muzikansky, A., Lobo, A. C., Tanabe, K. K., Sober, A. J., &... Duncan, L. M. (2015). Outcome of patients with de novo versus nevus-associated melanoma. Journal Of The American Academy Of Dermatology, 72(1), 54-58. doi:10.1016/j.jaad.2014.09.028 Marks, J. G., Miller, J. J., Lookingbill, D. P., & Lookingbill, D. P. (2006). Lookingbill and Marks' principles of dermatology. Philadelphia, PA: Saunders Elsevier. Ribero, S., Zugna, D., Osella-Abate, S., Glass, D., Nathan, P., Spector, T. and Bataille, V. (2016), Prediction of high naevus count in a healthy U.K. population to estimate melanoma risk. Br J Dermatol, 174: 312 318. doi:10.1111/bjd.14216 Werner RN, Jacobs A, Rosumeck S, Erdmann R, Sporbeck B, Nast A. Methods and Results Report - Evidence and consensus-based (S3) Guidelines for the Treatment of Actinic Keratosis - International League of Dermatological Societies in cooperation with the European Dermatology Forum. J Eur Acad Dermatol Venereol. 2015;29(11):e1-66. http://cms.sagepub.com/content/early/2016/07/19/1203475416659259 14