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Cutaneous angiomyolipoma (hereinafter described as “cutaneous AML”) is a benign tumor composed of varying proportions of thick-walled blood vessels, mature adipose tissue, and smooth muscle cells arranged in bundles, histologically identical to renal and extrarenal angiomyolipoma (hereinafter described as “classic AML”). Cutaneous AML is extremely rare and is not included in the latest 2018 World Health Organization (WHO) classification of skin tumors [1].
JMIR Dermatol 2022;5(3):e40168
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