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Superficial acral fibromyxoma impacts the palm, heel, and ankle in addition to the acral regions, with a clear preference for the periungual and subungual regions of the fingers and toes. [2] It begins as a slow-growing, solitary nodule limited to the dermis and subcutaneous tissue, and it is typically painless. [3]
Superficial acral fibromyxoma, also termed acral fibromyxoma. [15] Gardner fibroma, a benign proliferation of thick, irregularly arranged collagen bundles with interspersed fibroblasts often association with the genetic disease of familial adenomatous polyposis [23] and its variant, the Gardner's syndrome. [24
Acral angifibromeae occur primarily in areas close to the nails of fingers and toes (~80% of cases) [28] or, less commonly, palms of the hands or soles of the feet. [14] The tissues of this tumor consists of bland spindle-shaped and star-shaped cells within a collagen fiber -rich stroma containing prominent blood vessels and mast cells .
Acral myxoinflammatory fibroblastic sarcoma (AMSF), also termed myxoinflammatory fibroblastic sarcoma (MSF), is a rare, low-grade, soft tissue tumor that the World Health Organization (2020) classified as in the category of rarely metastasizing fibroblastic and myofibroblastic tumors. [1]
Myxoma is a rare, benign stromal tumor of mesenchymal origin often confused with other conjunctival stromal tumors. Conjunctival myxomas are thought to originate in Tenon's capsule and can masquerade as conjunctival lymphoma, lymphangioma, ocular surface squamous neoplasia (OSSN), or amelanotic melanoma.
Acral fibrokeratoma, also known as an acquired digital fibrokeratoma, and acquired periungual fibrokeratoma [1]: 668 is a skin lesion characterized by a pinkish, hyperkeratotic, hornlike projection occurring on a finger, toe, or palm.
Cutaneous myxoma appears as a little, slowly expanding dermal or subcutaneous lump that typically affects adults' heads and necks. [3] Alopecic lesions have been reported, [4] [5] characterized by hair tufts overlaying the lesion or even hypertrichosis. [6]
Angiolipoleiomyoma is an acquired, solitary, asymptomatic acral nodule, characterized histologically by well-circumscribed subcutaneous tumors composed of smooth muscle cells, blood vessels, connective tissue, and fat.