No familial or genetic component has been identified, and there appears to be no preference for sex or geographic or ethnic population. The cases of apocrine poroma in the literature have been only described in adults over the age of 40; however, due to its rarity, occurrence in children cannot be excluded. No pathogenetic mechanism has been identified.
Apocrine poroma has been referred to by several names including sebocrine adenoma, complex poroma-like adenoma, apocrine adenoma, and poroma with sebaceous differentiation.
D23.9 – Other benign neoplasm of skin, unspecified
403933005 – Sebaceoma
- Eccrine poroma – histopathology will not show sebaceous or follicular differentiation
- Seborrheic keratosis
- Basal cell carcinoma
- Nevus sebaceus – will be present at birth
- Sebaceous adenoma
- Infundibular adenoma
- Verruca vulgaris with sebaceous differentiation
- Extramammary Paget disease
- Pyogenic granuloma – these tend to bleed very easily
- Dermatofibroma – will have positive "dimple sign"
- Squamous cell carcinoma
- Trichoblastoma – these lack epidermal connection on histology