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Angiokeratoma circumscriptum in a young male
Dinkar Sadana1, Yugal K Sharma1, Kedarnath Dash1
1Department of Dermatology, Dr. D. Y. Patil Medical College and Hospital, Pimpri, Pune, Maharashtra, India.
This case report details a rare instance of angiokeratoma circumscriptum (AKC) in a young male, a condition typically affecting females. Successful surgical excision and skin grafting provided a favorable cosmetic outcome.
Area of Science:
- Dermatology
- Vascular Malformations
- Neoplastic Disease
Background:
- Angiokeratomas are vascular ectasias of the papillary dermis.
- Angiokeratoma circumscriptum (AKC) is the rarest variant, typically showing female predominance.
- AKC is an extremely rare nevoid disorder with limited reported cases.
Purpose of the Study:
- To report a case of angiokeratoma circumscriptum in a young male.
- To highlight diagnostic challenges and the importance of accurate counseling.
- To present a successful treatment outcome for AKC.
Main Methods:
- Clinical examination of a 20-year-old male with congenital leg lesions.
- Histopathological analysis confirming hyperkeratosis, acanthosis, and vascular proliferation.
- Surgical excision and skin grafting for treatment.
Main Results:
- The patient presented with painful, verrucous linear plaques on the right leg.
- Histopathology confirmed angiokeratoma circumscriptum.
- Excision and skin grafting resulted in a cosmetically favorable outcome.
Conclusions:
- Angiokeratoma circumscriptum can occur in males, contrary to its typical female preponderance.
- Accurate diagnosis and appropriate counseling are crucial for managing AKC.
- Surgical intervention can achieve favorable cosmetic results for AKC.
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