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Pigmented lesion clinic - Goals and Objectives - Dermatology

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<strong>Goals</strong> <strong>and</strong> <strong>Objectives</strong> <strong>Pigmented</strong> Lesion Clinic<br />

First-Year Residents:<br />

PIGMENTED LESION CLINIC<br />

RES C<br />

As a dermatologist you will become an expert on skin cancer, as well as a the main<br />

<strong>clinic</strong>al advisor for patients at risk. You have to be able to perform a thorough total<br />

body investigation to identify potential skin cancers <strong>clinic</strong>ally, <strong>and</strong> to decide whether a<br />

<strong>lesion</strong> will require total excision or further follow-up. Dermoscopy is a great tool for the<br />

diagnosis of early melanoma <strong>and</strong> other pigmented <strong>and</strong> non-pigmented tumors of the<br />

skin.<br />

This means you will have to:<br />

1. Recognize the <strong>clinic</strong>al features of common nevi, atypical nevi, melanoma, <strong>and</strong> other<br />

pigmented skin <strong>lesion</strong>s (pigmented BCC, seborrhoeic keratoses, angiomas, etc.)<br />

2. Learn the basic terminology used to describe pigmented <strong>lesion</strong>s examined with a<br />

dermoscope<br />

3. Learn the dermoscopic algorithm to differentiate between melanocytic <strong>and</strong> nonmelanocytic<br />

pigmented <strong>lesion</strong>s<br />

4. Learn one of the dermoscopic algorithms to diagnose melanoma <strong>and</strong> be able to use<br />

it in your daily routine (see readings below)<br />

Required Readings for First-Year Residents:<br />

1. Thompson JF et al. Cutaneous melanoma. Lancet 365:687-701, 2005<br />

2. Braun RP et al. Dermoscopy of pigmented skin <strong>lesion</strong>s. J Am Acad Dermatol:109-21,<br />

2005<br />

3. Kittler H et al. Diagnostic accuracy of dermoscopy. Lancet Oncol 3:159-65, 2002<br />

4. Curtin JA et al: Distinct sets of genetic alterations in melanoma. N Engl J Med<br />

353:2135-47, 2005<br />

5. Nachbar F, Stolz W et al. The ABCD rule of dermatoscopy. High prospective value in<br />

the diagnosis of doubtful melanocytic skin <strong>lesion</strong>s. J Am Acad Dermatol. 30:551-9,<br />

1994<br />

or<br />

Argenziano G et al. Epiluminescence microscopy for the diagnosis of doubtful<br />

melanocytic skin <strong>lesion</strong>s. Comparison of the ABCD rule of dermatoscopy <strong>and</strong> a new<br />

7-point checklist based on pattern analysis. Arch Dermatol. 134:1563-70, 1998<br />

or<br />

Menzies SW et al. A sensitivity <strong>and</strong> specificity analysis of the surface microscopy<br />

features of invasive melanoma. Melanoma Res. 6:55-62, 1996


<strong>Goals</strong> <strong>and</strong> <strong>Objectives</strong> <strong>Pigmented</strong> Lesion Clinic<br />

Second-Year Residents:<br />

PIGMENTED LESION CLINIC<br />

RES C<br />

You will learn to identify patients at increased risk for melanoma or who already have<br />

melanoma, <strong>and</strong> to manage, educate, encourage, <strong>and</strong> lead them. By improving your<br />

dermoscopy skills, <strong>and</strong> using short-term <strong>and</strong> long-term follow-up, you will improve<br />

early detection of melanoma <strong>and</strong> other skin cancers, <strong>and</strong> reduce unnecessary<br />

excisions, i.e. improve sensitivity <strong>and</strong> specificity of your melanoma diagnosis.<br />

In more detail, you will:<br />

1. Be able <strong>and</strong> confident in identifying <strong>lesion</strong>s suspicious for melanoma, <strong>and</strong> other<br />

pigmented tumors of the skin using dermoscopy.<br />

2. Be familiar with dermoscopic patterns suggestive for melanoma <strong>and</strong> other pigmented<br />

<strong>lesion</strong>s, as well as with the concept of “featureless melanoma”.<br />

3. Be able to outline a patient’s melanoma risk integrating patient’s common <strong>and</strong><br />

atypical melanocytic nevus counts, skin type, history, family history, <strong>and</strong> other<br />

factors.<br />

4. Learn to manage patients at high risk for melanoma, including required surgery, <strong>and</strong><br />

short- <strong>and</strong> long-term follow-up using digital images. You will learn the advantages<br />

<strong>and</strong> disadvantages of shave biopsies versus complete excisions.<br />

5. Be able to raise patient awareness of melanocytic nevi <strong>and</strong> melanoma risk without<br />

creating fear. You will also be able to educate patients regarding skin selfexamination,<br />

sun-protection, <strong>and</strong> required follow-up visits.<br />

6. Learn dermoscopic features of acral <strong>and</strong> facial pigmented tumors.<br />

Required Second-Year Readings:<br />

1. Bauer J, Garbe C. Acquired melanocytic nevi as risk factor for melanoma<br />

development. A comprehensive review of epidemiological data. Pigment Cell Res.<br />

16:297-306, 2003<br />

2. Pehamberger H, et al. In vivo epiluminescence microscopy of pigmented skin<br />

<strong>lesion</strong>s. I. Pattern analysis of pigmented skin <strong>lesion</strong>s. J Am Acad Dermatol 17:571-<br />

83, 1987<br />

3. Steiner A, et al. In vivo epiluminescence microscopy of pigmented skin <strong>lesion</strong>s. II.<br />

Diagnosis of small pigmented skin <strong>lesion</strong>s <strong>and</strong> early detection of malignant<br />

melanoma. J Am Acad Dermatol 17:584-91, 1987<br />

4. Menzies SW. Cutaneous melanoma: making a <strong>clinic</strong>al diagnosis, present <strong>and</strong> future.<br />

Dermatol Ther. 19:32-9, 2006<br />

5. Kittler H et al. Identification of <strong>clinic</strong>ally featureless incipient melanoma using<br />

sequential dermoscopy imaging. Arch Dermatol. 142:1113-9, 2006<br />

6. Stolz W at al. Dermatoscopy for facial pigmented skin <strong>lesion</strong>s. Clin Dermatol. 20:276-<br />

8, 2002<br />

7. Saida et al. Dermoscopy for acral pigmented skin <strong>lesion</strong>s. Clin Dermatol. 20:279-85,<br />

2002

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