Cutaneous collagenous vasculopathy
Individuals present with diffuse telangiectasias, initially on the lower extremities, that progressively spread to the trunk and upper extremities. Lesions typically spare the head and neck, but involvement of these areas has been observed. Telangiectasias are usually asymptomatic, but associated pruritus or pain has been reported. They also characteristically spare the mucosa and nails, but a 2018 case documented recurrent bleeding from gastric mucosal telangiectasias requiring multiple transfusions.
I73.89 – Other specified peripheral vascular diseases
718634003 – Cutaneous collagenous vasculopathy
- Generalized essential telangiectasia (GET) – Clinically indistinguishable. Histology shows dilated capillaries or postcapillary venules in the superficial dermis without thickened walls.
- Hereditary hemorrhagic telangiectasia (HHT) – Systemic involvement, family history, and early onset.
- Hereditary benign telangiectasia – Family history and early onset.
- Telangiectasia macularis eruptiva perstans
- Ataxia-telangiectasia syndrome
- Angioma serpiginosum
- Drug-induced telangiectasias – Calcium channel blockers and interferon alpha most commonly. Histology shows dilated superficial capillaries without thickening of the vessel walls.
- Collagen vascular diseases (eg, scleroderma, dermatomyositis, lupus erythematosus)
- Primary amyloidosis