Abstract:A 52-year-old Japanese woman presented with a 1.5-cm black, glossy, flat, pediculated lump that clinically mimicked a melanocytic nevus on the left temporal side of her head. The subcutaneous tumor beneath the nodule was elastic and hard. A histological examination showed that the tumor was well circumscribed with an exo-and endophytic growth 2.4 × 1.9 cm in size. The lesion contained several keratinous cysts and was composed of funicular fascicles containing squamoid cells. Excessive mucinous material deposit… Show more
“…However, morphological variations with lesions clinically mimicking melanocytic naevus and seborrhoeic keratosis have been described. 3,4 The importance of recognising this rare variant of BCC in dark skin phototype is twofold. Firstly, it needs to be differentiated from other variants of BCC due to its less aggressive behaviour as most of the lesions are slow-growing small tumours without ulceration.…”
mentioning
confidence: 99%
“…It can occur as a solitary lesion or as a part of multiple hereditary infundibulocystic basal cell carcinoma syndrome. 2,3 The solitary form typically presents as a well-circumscribed slow-growing small (average diameter: 1-10 mm) dome-shaped superficial pearly papule or dermal nodule commonly on the face. However, morphological variations with lesions clinically mimicking melanocytic naevus and seborrhoeic keratosis have been described.…”
In conclusion, SCLE induced by PD-1 Inhibitor therapy is a rarely reported adverse effect, which can be persistent after immunotherapy discontinuation. Treatment withholding and systemic corticosteroids and/or hydroxychloroquine are usually needed.
“…However, morphological variations with lesions clinically mimicking melanocytic naevus and seborrhoeic keratosis have been described. 3,4 The importance of recognising this rare variant of BCC in dark skin phototype is twofold. Firstly, it needs to be differentiated from other variants of BCC due to its less aggressive behaviour as most of the lesions are slow-growing small tumours without ulceration.…”
mentioning
confidence: 99%
“…It can occur as a solitary lesion or as a part of multiple hereditary infundibulocystic basal cell carcinoma syndrome. 2,3 The solitary form typically presents as a well-circumscribed slow-growing small (average diameter: 1-10 mm) dome-shaped superficial pearly papule or dermal nodule commonly on the face. However, morphological variations with lesions clinically mimicking melanocytic naevus and seborrhoeic keratosis have been described.…”
In conclusion, SCLE induced by PD-1 Inhibitor therapy is a rarely reported adverse effect, which can be persistent after immunotherapy discontinuation. Treatment withholding and systemic corticosteroids and/or hydroxychloroquine are usually needed.
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