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CASE REPORT
Year : 2015  |  Volume : 16  |  Issue : 3  |  Page : 165-167

Angiokeratoma circumscriptum in a child of Klippel-Trenaunay syndrome: A rare association


Department of Dermatology, Venereology and Leprosy, BYL Nair charitable Hospital and T. N. Medical College, Mumbai, India

Correspondence Address:
Dipti Das
Flat No. 706, E Wing, Trans Residency 1, Subhash Nagar, MIDC, Road-23, Andheri East, Mumbai - 400 093, Maharashtra
India
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Source of Support: Nil., Conflict of Interest: There are no conflicts of interest.


DOI: 10.4103/2319-7250.160671

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Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterized by capillary malformation, vascular anomalies, and bony and soft tissue hypertrophy. Angiokeratomas are of several types. Angiokeratoma circumscriptum (AC) is a nevoid form which presents as dark red papules and plaques mostly with a verrucous surface. AC is itself very rare. KTS along with AC is even rarer. Here, we present a rare case of KTS with AC on the background of port-wine stain.


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