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A venous lake (also known as phlebectasis [1]) is a generally solitary, soft, compressible, dark blue to violaceous, 0.2- to 1-cm papule commonly found on sun-exposed surfaces of the vermilion border of the lip, face and ears. [2] [3] [4] Lesions generally occur among the elderly. [5] [6]
Angiosarcoma is a rare and aggressive cancer that starts in the endothelial cells that line the walls of blood vessels or lymphatic vessels.Since they are made from vascular lining, they can appear anywhere and at any age, but older people are more commonly affected, and the skin is the most affected area, with approximately 60% of cases being cutaneous (skin).
Angiokeratoma may be classified as: Angiokeratoma of Mibelli (also known as "Mibelli's angiokeratoma," [4] "Telangiectatic warts" [5]) consists of 1- to 5-mm red vascular papules, the surfaces of which become hyperkeratotic in the course of time.
A vascular tumor is a vascular anomaly where a tumor forms from cells that make blood or lymph vessels; a soft tissue growth that can be either benign or malignant. [1] ...
Melanoma is a malignant proliferation of melanocytes and the most aggressive type of skin cancer. [80] [81] [82] Acral lentiginous melanoma Nodular melanoma; Amelanotic melanoma; Animal-type melanoma; Desmoplastic melanoma (neurotropic melanoma, spindled melanoma) Lentigo maligna (lentiginous melanoma on sun-damaged skin) Lentigo maligna melanoma
Evolution of a 4 mm nodular melanoma. Nodular melanoma (NM) is the most aggressive form of melanoma. [1] It tends to grow more rapidly in thickness (vertically penetrate the skin) than in diameter compared to other melanoma subtypes. [2] Instead of arising from a pre-existing mole, it may appear in a spot where a lesion did not previously exist.
Blue nevi may be divided into the following types: [7]: 701 A patch blue nevus (also known as an "acquired dermal melanocytosis", and "dermal melanocyte hamartoma") is a cutaneous condition characterized by a diffusely gray-blue area that may have superimposed darker macules.
The most successful treatment for lymphangiosarcoma is amputation of the affected limb if possible. Chemotherapy may be administered if there is evidence or suspicion of metastatic disease. Evidence supporting the effectiveness of chemotherapy is, in many cases, unclear due to a wide variety of prognostic factors and small sample size.
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