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Klippel Trenaunay Syndrome: A Case Report
M N Islam1, M A Hossain, M S Rahman
1Dr Md Nazrul Islam, Assistant Professor, Department of Neonatology, Mymensingh Medical College, Mymensingh, Bangladesh; E-mail; mnislamdr1@yahoo.com.
Mymensingh Medical Journal : MMJ
|December 13, 2016
Summary
Klippel Trenaunay Syndrome is a rare congenital condition causing limb overgrowth and vascular malformations. This case highlights a preterm neonate presenting with typical Klippel Trenaunay Syndrome features at birth.
Area of Science:
- Vascular Malformations
- Pediatric Genetics
- Congenital Anomalies
Background:
- Klippel Trenaunay Syndrome (KTS) is a rare congenital disorder.
- It is characterized by a triad of capillary, venous, and lymphatic malformations.
- KTS is often associated with limb overgrowth, including soft tissue and bony hypertrophy.
Observation:
- This report details a preterm male neonate.
- The neonate presented with a port wine stain, varicose veins, and excessive soft tissue growth.
- These clinical features were observed on the left lower limb.
Findings:
- The observed clinical presentation is consistent with Klippel Trenaunay Syndrome.
- The condition was evident at birth in the neonate.
- The affected limb showed significant soft tissue hypertrophy.
Implications:
- Early recognition of Klippel Trenaunay Syndrome is crucial for timely management.
- This case underscores the importance of recognizing KTS in neonates with vascular anomalies and limb overgrowth.
- Further research into the genetic and developmental origins of KTS is warranted.
