Angiokeratoma
(Redirected from Angiokeratoma circumscriptum naeviforme)
Introduction[edit | edit source]
Angiokeratoma (pronounced an-je-o-ker-at-o'-mah) is a rare skin condition characterized by small, dark vascular lesions that resemble warts. These lesions typically develop on dilated blood vessels in individuals with certain predisposing conditions, such as chilblains.
Definition and Characteristics[edit | edit source]
Angiokeratoma is a medical term combining "angio-" (referring to blood vessels), "kerat-" (from Greek 'Kerat,' meaning horn, indicating a hard texture), and "-oma" (denoting a tumor or growth). The condition is marked by:
- Warty-looking growths on dilated vessels.
- Dark vascular spots ranging in size from pin-points to pin-heads.
- A predilection for occurring in childhood.
Pathogenesis and Etiology[edit | edit source]
- Chilblains: Angiokeratomas often develop as an attack of chilblains is subsiding. Chilblains are small, itchy, red patches that can appear after exposure to cold.
- Vascular Dilatation: The condition involves the dilatation of blood vessels near the skin's surface.
Clinical Presentation[edit | edit source]
- Angiokeratoma lesions typically appear on the extremities.
- They are often dark red to black in color and have a rough surface.
- The condition is more common in children, but can occasionally be seen in adults.
Diagnosis[edit | edit source]
Diagnosis of angiokeratoma generally involves:
- Clinical examination of the characteristic lesions.
- Dermatoscopic evaluation to observe the vascular patterns.
- Biopsy and histopathological examination in uncertain cases.
Treatment and Management[edit | edit source]
While angiokeratomas are usually benign and asymptomatic, treatment options may be considered for cosmetic reasons or discomfort, including:
- Laser therapy.
- Cryotherapy.
- Surgical excision in rare cases.
Complications[edit | edit source]
In rare instances, angiokeratomas may be associated with systemic diseases, or complications such as bleeding may occur from the lesions.
Prognosis[edit | edit source]
The prognosis for isolated angiokeratomas is generally good, especially in children where the condition may resolve spontaneously.
Epidemiology[edit | edit source]
This condition is relatively rare and has a higher incidence in individuals with a history of chilblains or other vascular conditions.
References[edit | edit source]
External Links[edit | edit source]
See Also[edit | edit source]
Angiokeratoma Resources | |
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Contributors: Prab R. Tumpati, MD