| CASE REPORT |
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| Year : 2020 | Volume
: 11
| Issue : 3 | Page : 404-408 |
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Klippel–Trenaunay syndrome with arterio-veno-lymphatic malformation: A rare presentation
Bhagyashree B Supekar1, Apoorva D Chopkar1, Vaishali H Wankhade1, Rajesh Pratap Singh1, Dharitri Mukund Bhat2, Parvathy Suresh3
1 Department of Dermatology, Venereology and Leprology, Government Medical College and Hospital, Nagpur, Maharashtra, India
2 Department of Pathology, Government Medical College and Hospital, Nagpur, Maharashtra, India
3 Department of Radiology, Government Medical College and Hospital, Nagpur, Maharashtra, India
Correspondence Address:
Vaishali H Wankhade
Department of Dermatology, Venereology and Leprology, Government Medical College Nagpur - 440 003, Maharashtra
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/idoj.IDOJ_220_19
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Klippel–Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity. Port wine stain is the most common vascular malformation associated with this syndrome. Various other rare vascular malformations described are angiokeratomas, angiokeratoma circumscriptum naeviformae, angiodermatitis, etc. This is the first instance, to the best of our knowledge, describing the capillary, venous, and lymphatic malformations in a same case of KTS.
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