Author: A/Prof Patrick Emanuel, Dermatopathologist, Auckland, New Zealand, 2014.
Melanocytic matricoma is a rare tumour that presents as a small heavily pigmented tumour. It clinically mimics nodular melanoma, haemangioma and other pigmented tumours. So far, these tumours have exhibited a benign clinical course.
Histology of melanocytic matricoma
Sections through melanocytic matricoma show a well-circumscribeddermaltumour which may encroach and erode the overlying epidermis (figure 1). There is heavy melanindeposition. The tumour is made up of basaloid cells with some nuclear pleomorphism and conspicuous mitotic activity. Intermixed with these epithelial cells are a population of dendritic melanocytes (figures 1-4). There is focal “ghost cell” keratinisation (figures 5, 6).
Keratin stains confirm that the tumour is epithelial (rather than a melanoma). Melanocytic stains demonstrate a population of intermixed dendritic melanocytes.
Differential diagnosis of melanocytic matricoma
Melanoma – These tumours may mimic melanoma clinically and histologically (the case illustrated herein was initially diagnosed a melanoma both clinically and histologically). Immunohistochemical studies can help exclude this possibility. Keratinisation should not be seen in melanoma.
Basal cell carcinoma – BCC can show focal matrical differentiation. However, other features such as stromal retraction and peripheral palisading should be seen with BCC.
Malignant matricoma – Malignancy in matrical tumours can be difficult to exclude in small biopsies given the marked pleomorphism and mitoses which are common in benign matrical tumours. Deep invasion, necrosis and large clinical size can be helpful features in diagnosing a malignanttumour.
Pathology of the Skin (Fourth edition, 2012). McKee PH, J. Calonje JE, Granter SR