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Earlier this week, we shared our third Skin Cancer Awareness Month quiz. Review the answers and your responses below.
This week we asked the question: How much do you know about dermoscopy and melanoma detection?
Haven't taken our quiz yet? Pause before reading below and follow this link to complete it: here.
Below, we recap our third quiz and the correct answers to each question.
Response options:
Correct response option: Dermatofibroma
Dermatofibroma is characterized by an increase in fibrocytes in the dermis and sometimes the subcutis, and includes a mix of macrophages and inflammatory cells like lymphocytes, and rarely eosinophils, neutrophils, and plasma cells. Dermatofibromas typically present as firm, single or multiple hard papules, plaques, or nodules with a smooth surface and variable color, often occurring on the lower extremities and is dermoscopically characterized by a “negative” of the pigment network.1
Response options:
Correct response option: Suggestive of melanoma
A key diagnostic feature of melanoma in dermoscopy images is the blue-white veil, which consists of irregular, structureless blue areas with an overlying white "ground-glass" film.2
Response options:
Correct response option: Hairpin vessels
In irritated seborrheic keratosis, hairpin-like vessels may become elongated, twisted, and branched. These vessels can show up as dark red dots in flat lesion areas and can take on perfect "U" shapes or twisted "U" shapes. Typical hairpin vessels are surrounded by a whitish halo, which is the keratin around them.3
Response options:
Correct response option: Blue-gray ovoid nests
A 2019 NCBI study identified the most common dermoscopic features of basal cell carcinoma (BCC) as follows: arborizing vessels in 59% of cases, shiny white structures in 49%, and large blue-grey ovoid nests in 34%.4
Response options:
Correct response option: True
Dermoscopy screening for melanoma involves a 3-point checklist: assessing asymmetry (due to variations in pigment network thickness, tumor regression areas, or unevenly distributed pigment globules), identifying atypical pigment networks (with thick branches and lack of peripheral fading), and spotting blue-colored areas. If a lesion shows more than one of these features, it should be biopsied, monitored, or the patient referred to a dermatologist.5
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