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Klippel-Trenaunay syndrome.
Rashid Rasheed1, Durr-e-Sabih, Muhammad Kashif Rahim
1Department of Nuclear Medicine, Multan Institute of Nuclear Medicine and Radiotherapy, Nishtar Hospital, Multan.
Klippel-Trenaunay Syndrome (KTS) is a rare vascular disorder. This case highlights diagnostic findings in a young woman with leg swelling and a limp, confirming KTS.
Area of Science:
- Vascular Medicine
- Medical Imaging
- Genetics
Background:
- Klippel-Trenaunay Syndrome (KTS) is a congenital vascular malformation.
- KTS classically presents with a triad of port-wine stains, varicose veins, and limb hypertrophy.
- Diagnosis can be challenging due to variable clinical manifestations.
Observation:
- A 20-year-old female presented with a limp and right leg swelling.
- Doppler ultrasonography revealed dilated arteries and increased blood flow velocity in the affected limb.
- The patient's clinical presentation was further evaluated with nuclear medicine and radiological imaging.
Findings:
- Diagnostic imaging confirmed findings consistent with Klippel-Trenaunay Syndrome.
- The case underscores the utility of advanced imaging in diagnosing KTS.
- Specific radiological and nuclear medicine findings supported the KTS diagnosis.
Implications:
- Early and accurate diagnosis of KTS is crucial for appropriate management.
- Understanding the vascular anomalies in KTS aids in predicting disease progression.
- This case contributes to the literature on KTS diagnostic modalities.
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