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Epidermoid Cyst

Also known as: Epidermal Inclusion Cyst

Epidermoid cysts (commonly misnamed sebaceous cysts) are benign, slowly growing, intradermal or subcutaneous cysts lined by stratified squamous epithelium and filled with laminated keratin. They are the commonest cutaneous cyst, and affect about 1 in 20 people, more often men and adults after puberty.

Pathogenesis

  • Implantation of epidermis into the dermis after trauma, or occlusion of the pilosebaceous follicular infundibulum (follicular cyst).
  • Lining epithelium has a granular layer and produces keratin, which accumulates. Rupture releases keratin into the dermis, causing an intense foreign-body inflammatory reaction that mimics infection.
  • Associated conditions: acne vulgaris (open comedones), hidradenitis, and Gardner syndrome (familial adenomatous polyposis: multiple epidermoid cysts, osteomas, desmoid tumours, colorectal polyps, often on the scalp and face). Other syndromes: basal cell nevus syndrome, pachyonychia congenita type 2.
  • HPV 57-related plantar epidermoid cysts.

Related cysts

  • Pilar (trichilemmal) cyst: scalp (90%), lined by trichilemmal keratin with no granular layer, firmer, familial (autosomal dominant), more in women. Proliferating trichilemmal tumour is a rare variant.
  • Milia: tiny superficial keratin cysts.
  • Steatocystoma multiplex: multiple sebaceous duct cysts with oily fluid (KRT17 mutations).
  • Dermoid cyst: congenital, along embryonic fusion lines, contains hair and adnexae.
  • Complications: inflammation or secondary infection (in 10 to 15%), abscess, rupture, calcification, rare malignant transformation (squamous cell carcinoma, basal cell carcinoma in long-standing lesions, over 0.1%), and recurrence after incomplete excision.

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