In simple words: This is a rare skin condition that causes changes in skin color, visible blood vessels, and thinning of the skin.

Poikiloderma vasculare atrophicans is a rare skin disorder that can resemble chronic radiodermatitis. It is often considered a variant of mycosis fungoides, a type of cutaneous T-cell lymphoma.

Example 1: A patient presents with mottled skin discoloration, prominent blood vessels, and thinning of the skin on their arms and legs. After a thorough examination and skin biopsy, they are diagnosed with poikiloderma vasculare atrophicans., A dermatologist examines a patient with a history of lymphoma. The patient exhibits patchy skin discoloration with telangiectasia and atrophy, suggestive of poikiloderma vasculare atrophicans. Further investigation is done to rule out disease progression or recurrence., A patient undergoing treatment for mycosis fungoides develops skin changes including hyperpigmentation, hypopigmentation, telangiectasia, and atrophy. These findings indicate the development of poikiloderma vasculare atrophicans as a complication of their underlying condition.

Documentation should include a detailed description of the skin lesions, including their location, size, color, and texture.Any relevant history, such as previous lymphoma or other skin conditions, should be noted.Results of any diagnostic tests, such as skin biopsies, should also be included.

** Poikiloderma vasculare atrophicans is a rare condition, and its etiology is not fully understood. It can occur as a primary disorder or secondary to other conditions, such as mycosis fungoides. The condition is typically chronic and progressive.