Final answer:
Steatocystoma multiplex is an inherited benign condition causing multiple sebum-filled cysts, associated with KRT17 gene mutations, and treatment usually involves minor surgical procedures.
Step-by-step explanation:
Steatocystoma multiplex is a benign, inherited condition characterized by the development of multiple noncancerous cysts that are filled with sebum. These cysts typically appear during adolescence or early adulthood and are often found clustered on the torso, neck, upper arms, underarms, and thighs. The cysts are usually harmless but can occasionally become inflamed or infected, causing discomfort. This skin disorder is associated with mutations in the KRT17 gene, which plays a role in the development of hair follicles, nails, and certain types of epithelial cells. Treatment options for steatocystoma multiplex primarily consist of minor surgical procedures or needle aspiration to remove or drain the cysts, improving comfort and cosmetic appearance.