Anatomic Pathology: Skin Pathology

741) A 40-year-old woman suddenly developed a 2-cm, blue-black nodule on the right thigh. Because of her strong family history of melanoma, her family physician referred her to a surgeon for excision of the lesion. The biopsy specimen is shown. The pathologic diagnosis is:

• Several terms have been used for dermatofibroma, including histiocytoma, fibrous histiocytoma, sclerosing hemangioma, and nodular subepidermal fibrosis, which reflect the variation in its histologic findings and controversy in its histogenesis.

• Histopathologically, dermatofibromas are composed of a variable mixture of fibroblast-like cells, histiocytes (some of which may be xanthomatous or multinucleate), and blood vessels. These different cells reflect the multiple subtypes of dermatofibroma.

• The hemosiderotic type of dermatofibroma is characterized by a proliferation of predominantly multinucleated histiocytes containing lipid and hemosiderin. Capillaries may be plentiful in the stroma in the angiomatous (aneurysmal) subtype. When there is associated sclerosis, such lesions have been referred to as sclerosing hemangioma.

• The histologic features of several variants of dermatofibroma can coexist in the same lesion and may correspond to different stages of the same disease.

• The epidermal changes of dermatofibromas include acanthosis, hyperkeratosis, and basal layer hyperpigmentation with elongation of rete ridges. In some cases, the changes resemble a seborrheic keratosis or may exhibit basaloid hyperplasia with follicular induction. Sebaceous structures and sebaceous hyperplasia uncommonly are present.

 
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