Poikiloderma vasculare atrophicans
PVA is characterized by atrophic patches with telangiectasia and mottled pigmentation, usually on the trunk and flexural areas. The condition is typically asymptomatic; however, there may be pruritus.
Onset is typically between 40 and 60 years of age, with a slight male predilection. Initial presentation may be with one to a few patches that persist for many years. Over time, the lesions may remain stable in size or gradually enlarge or thicken as well as increase in number. Wrinkled, thin plaques that are not poikilodermatous and that resemble patch-stage MF may also be present.
Progression to a more advanced stage of MF is not reliably predictable, and the disease may remain quiescent for many years or indefinitely.
L94.5 – Poikiloderma vasculare atrophicans
16341002 – Poikiloderma vasculare atrophicans
Differential Diagnosis & Pitfalls
- Burns (see ; chemical burns are covered separately, by chemical agent)
- – Poikilodermatous changes are usually in areas of chronic erythema; histologic findings are consistent with connective tissue disease, eg, dermal mucin and interface changes.
- Acrodermatitis chronica atrophicans – A late stage of active infection with Borrelia afzelii. Affected areas may have dark-reddish discoloration; cryoglobulins are positive in the majority of patients.
- – Presents with indurated lesions initially with progression to atrophy with a violaceous border.
- – Presents as ivory to porcelain-white colored plaques and papules with fissuring, telangiectasia, and sometimes erosion.
- – Erythema with mottled hyperpigmentation, usually on the sun-exposed areas of the neck and upper chest.
- Genodermatoses including (poikiloderma congenitale), (congenital telangiectatic erythema), , , and – Usually will have other history and findings associated with syndrome.